Semiconductor materials prepared from bridged bithiazole copolymers

Abstract

The present invention provides semiconducting compounds, oligomers and polymers of formula

Description

Organic semiconducting materials can be used in electronic devices such as organic photovoltaic (OPV) cells, organic field-effect transistors (OFETs) and organic light emitting diodes (OLEDs).

It is desirable that the organic semiconducting materials are compatible with liquid processing techniques such as spin coating, solution casting or printing. Liquid processing techniques are convenient from the point of processability, and can also be applied to plastic substrates. Thus, organic semiconducting materials which are compatible with liquid processing techniques allow the production of low cost, light weight and, optionally also flexible, electronic devices, which is a clear advantage of these organic semiconducting materials compared to inorganic semiconducting materials.

Furthermore, it is desirable that the organic semiconducting materials are stable, in particular towards oxidation.

When used in organic field-effect transistors (OFETs), the organic semiconducting materials should show a high charge carrier mobility and a high on/off ratio.

The use of organic semiconducting materials in electronic devices, in particular in organic field effect transistors (OFETs) is known in the art.

Fuchigami, H.; Tsumura, A.; Koezuka, H. Appl. Phys. Lett. 1993, 63, 1372-1374 describes the use of poly(2,5-thienylenevinylene) in field-effect transistors.

Bao, Z.; Dobadalapur, A.; Lovinger, A. J. Appl. Phys. Lett. 1996, 69, 4108-4110 describes the use of regioregular poly(3-hexylthiophene) in field-effect transistors.

Zhang, M.; Tsao, H. N.; Pisula, W.; Yang, C.; Mishra, A. K.; Müllen, K. J. Am. Chem. Soc. 2007, 129, 3472-3473 describes polymers of formula

for use in organic field effect transistors (OFETs).

Xiao, S; Zhou H.; You, W. Macromolecules 2008, 41, 5688-5696 describes the following polymers

as donor materials for use in photovoltaic devices.

Scharber, M. C.; Koppe, M.; Gao, J.; Cordella, F.; Loi, M. A.; Denk, P.; Morana, M.; Egelhaaf, H.-J.; Forberich, K.; Dennler, G.; Gaudiana, R.; Waller, D.; Zhu, Z.; Shi, X.; Brabec, C. J. Adv. Mater. 2009, 21, 1-4 describes the following polymers

as donor materials for use in solar cells.

Rieger, R.; Beckmann, D.; Pisula, W.; Steffen, W.; Kastler, M.; Müllen K. Adv. Mater. 2010, 22, 83-86 describes the following polymers

for use in organic field-effect transistor (OFET).

Kim, D. H.; Lee, B.-L-; Moon, H.; Kang, H. M.; Jeong, E. J.; Park, J.; Han, K.-M.; Lee, S.; Yoo, B. W.; Koo, B. W.; Kim, J. Y.; Lee, W. H.; Cho, K.; Becerril, H. A.; Z. Bao Z. J. Am. Chem. Soc. 2009, 131, 6124-6132 describes the polymer

for use in organic field effect transistors (OFETs).

Osaka, I.; Sauvé, G.; Zhang, R.; Kowalewski, T.; McCullough R. D. Adv. Mater. 2007, 19, 4160-4165 describes the polymers

for use in organic field effect transistors (OFETs).

EP 2 085 401 A1 describes benzobisthiazole polymers comprising a unit having the following formula

wherein each of R¹, R², R³ and R⁴ represents a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group or a substituted or unsubstituted thioalkoxy group, wherein at least one of R¹, R², R³ and R⁴ is not a hydrogen atom, and n is a positive integer, wherein when n is 2 or more, each of R³ is the same as or different from the others and each of R⁴ is the same or different from the others,for use in transistors.

US 2008/0121281 A1 describes photovoltaic cells with thiazole-containing polymers such as bithiazole-containing polymers, cyclopentadithiazole-containing polymers or thiazolothiazole-containing polymers. Cyclopentadithiazole-containing polymers can be polymers which include a first comonomer repeat unit comprising a cyclopentadithiazole moiety, and a second comonomer repeat unit different from the first comonomer repeat unit. In some embodiments, the first comonomer repeat unit includes a cyclopentadithiazole moiety of formula

in which each of R¹ and R², independently, is H, C_1-20-aklyl, C_1-20-alkoxy, C_3-20-cycloalkyl, C_1-20-heterocycloalkyl, aryl, heteroaryl, halo, CN, OR, C(O)R, C(O)OR, or SO₂R; R being H, C_1-20-alkyl, C_1-20-alkoxy, C_3-20-cycloalkyl, C_1-20-heterocycloalkyl, aryl, or heteroaryl.

WO 2009/069687 describes a polymer represented by the general formula

wherein Z²¹ and Z²² independently represent, for example, —S—.

It is the object of the present invention to provide organic semiconducting materials suitable for use in electronic devices, in particular in organic field effect transistors (OFETs), where the organic semiconducting materials show a high oxidative stability, particularly in ambient conditions, and are compatible with liquid processing techniques. The organic field effect transistors comprising the organic semiconducting materials should show an acceptable charge carrier mobility and current on/off ratio.

This object is solved by the compound, oligomer or polymer of claim 1 and the electronic device of claim 19.

The compound, oligomer or polymer of the present invention are of formula

wherein

• A¹ and A² can be the same or different and are S or Se,
• E is selected from the group consisting of

• • wherein
  • R¹ and R² can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X¹—R⁶, —X²—Ar¹, —X²—Ar²—Ar¹, —X²—Ar²—R⁷ or —X²—Ar²—Ar³—R⁷,
    • wherein
    • X¹ at each occurrence is independently —O—, —[Z¹—O]_a—, —[O—Z¹]_a—O—, —S—, —[Z¹—S—]_a—, —[S—Z¹]_a—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR⁸—, C(O)S—, —O(CO)—, —S(CO)—, —NR⁸C(O)— or —NR⁸—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
      • R⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²—C_6-14-aryl,
        • wherein
        • Z² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R⁶ at each occurrence is independently C_1-3-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR⁹, —C(O)S—, —O(CO)—, —S(CO)—, —NR⁹C(O)—, —NR⁹—, —Z³—SiR⁹₂—Z⁴—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R⁹ at each occurrence is independently H, C_1-20-alkyl, or —Z⁵—C_6-14-aryl,
        • wherein
        • Z⁵ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar² and Ar³ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^b, wherein each R^b is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X³—Ar⁴, —X³—Ar⁵—Ar⁴, —X³—Ar⁵—R¹⁰, or —X³—Ar⁵—Ar⁶—R¹⁰,
      • wherein
      • X³ at each occurrence is independently —Z⁶—O—Z⁷—, —Z⁶—S—Z⁷, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹¹, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹¹C(O)—, —NR¹¹—, —Z⁶—SiR¹¹₂—Z⁷—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z⁶ and Z⁷ at each occurrence are independently C_1-6-alkylene,
        • C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹¹ at each occurrence is independently H, C_1-20-alkyl or —Z⁸—C_6-14-aryl,
        •  wherein
        •  Z⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene,
        •  C_1-6-haloalkylene or a covalent bond,
      • Ar⁴ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^c, wherein each R^c is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar⁵ and Ar⁶ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^d, wherein each R^d is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
      • R¹⁰ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl,
      • C_1-20-haloalkyl or C_1-20-alkoxy,
  • R³, R⁴ and R⁵ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X⁴—R¹², —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,
    • wherein
    • X⁴ at each occurrence is independently —[Z⁹—O]_b—, —[Z⁹—S—]_b—, —S(O)—, —C(O)—, —C(O)O—, —C(O)NR¹⁴— or C(O)S—,
      • wherein
      • Z⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • b at each occurrence is independently an integer from 1 to 10 and
      • R¹⁴ at each occurrence is independently H, C_1-20-alkyl, or —Z¹⁰—C_6-14-aryl,
        • wherein
        • Z¹⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R¹² at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁵ at each occurrence is independently —Z¹¹—O—Z¹², —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁵, —C(O)S—, —Z¹¹—SiR¹⁵₂—Z¹²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z¹¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • Z¹² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R¹⁵ at each occurrence is independently H, C_1-20-alkyl, or —Z¹³—C_6-14-aryl,
        • wherein
        • Z¹³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
    • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁶—Ar¹⁰, —X⁶—Ar¹¹—Ar¹⁰, —X⁶—Ar¹¹—R¹⁶, or —X⁶—Ar¹¹—Ar¹²—R¹⁷,
      • wherein
      • X⁶ at each occurrence is independently —Z¹⁴—O—Z¹⁵—, —Z¹⁴—S—Z¹⁵—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹⁸C(O)—, —NR¹⁸—, —Z¹⁴—SiR¹⁸₂—Z¹⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z¹⁴ and Z¹⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹⁸ at each occurrence is independently H, C_1-20-alkyl or —Z¹⁶—C_6-14-aryl,
        •  wherein
        •  Z¹⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar¹⁰ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^g, wherein each R^g is independently selected from the group consisting of halogen, CN, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar¹¹ and Ar¹² at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^h, wherein each R^h is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
      • R¹⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
  • R¹⁹ is O or C(CN)₂, and
  • R²⁰ and R²¹ are the same or different and are R²² or CN, wherein R²² has the same meaning as R¹,
• G¹ and G² are the same or different and are phenylene or a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue, which phenylene and monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of halogen, —CN, —NO₂, —OH, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_5-10-cycloalkenyl, —Z¹⁷—C_8-10-cycloalkynyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_mH, —S(O)_m—C_1-20-alkyl, —S(O)₂OH, —S(O)_m—OC_1-20-alkyl, —S(O)_m—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_mNH₂, —S(O)_mNH(C_1-20-alkyl), —S(O)_mN(C_1-20-alkyl)₂, —S(O)_mNH(C_6-14-aryl), —S(O)_mN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_mN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • m at each occurrence is independently 0, 1 or 2,
• L is C_6-24-arylene or a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein C_6-24-arylene and bivalent 5 to 18 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, OH, *═C(C_1-30-alkyl)₂, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-30-cycloalkyl, —Z¹⁸—C_5-10-cycloalkenyl, —Z¹⁸—C_8-10-cycloalkynyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_oH, —S(O)_o—C_1-20-alkyl, —S(O)₂OH, —S(O)_o—OC_1-20-alkyl, —S(O)_o—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_oNH₂, —S(O)_oNH(C_1-20-alkyl), —S(O)_oN(C_1-20-alkyl)₂, —S(O)_oNH(C_6-14-aryl), —S(O)_oN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_oN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, —S—C_1-20-alkyl, C_1-20-haloalkyl,
• wherein
• Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
• o at each occurrence is independently 0, 1 or 2,or
• L is

• • wherein
  • R²³ and R²⁴ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar¹⁴—R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,
    • wherein
    • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_c—, —[O—Z¹⁹]_c—O—, —S—, —[Z¹⁹—S—]_c—, —[S—Z¹⁹]_c—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR²⁷—, C(O)S—, —O(CO)—, —S(CO)—, —NR²⁷C(O)— or —NR²⁷—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
      • R²⁷ at each occurrence is independently H, C_1-20-alkyl, or C_6-14-aryl,
        • wherein
        • Z²⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR²⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR²⁸C(O)—, —NR²⁸—, —Z²¹—SiR²⁸₂—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R²⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²³—C_6-14-aryl,
        • wherein
        • Z²³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹³ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁹—Ar¹⁶, —X⁹—Ar¹⁷—Ar¹⁶, —X⁹—Ar¹⁷—R²⁹, or —X⁹—Ar¹⁷—Ar¹⁸—R²⁹,
      • wherein
      • X⁹ at each occurrence is independently —Z²⁴—O—Z²⁵—, —Z²⁴—S—Z²⁵, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR³⁰, —C(O)S—, —O(CO)—, —S(CO)—, —NR³⁰C(O)—, —NR³⁰—, —Z²⁴—SiR³⁰₂—Z²⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z²⁴ and Z²⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R³⁰ at each occurrence is independently H, C_1-20-alkyl or —Z²⁶—C_6-14-aryl,
        •  wherein
        •  Z²⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar¹⁶ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^q, wherein each R^q is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar¹⁷ and Ar¹⁸ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^r, wherein each R^r is independently selected from the group consisting of halogen, CN, C_1-6-alkoxy and C_1-6-haloalkyl, and
      • R²⁹ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
• q and s are the same or different and are 0, 1, 2, 3, 4 or 5,
• r is 0, 1 or 2,and
• n is an integer from 1 to 10,000.

Preferred are oligomers or polymers of formula

wherein

• A¹ and A² can be the same or different and are S or Se,
• E is selected from the group consisting of

• • wherein
  • R¹ and R² can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X¹—R⁶, —X²—Ar¹, —X²—Ar²—Ar¹, —X²—Ar²—R⁷ or —X²—Ar²—Ar³—R⁷,
    • wherein
    • X¹ at each occurrence is independently —O—, —[Z¹—O]_a—, —[O—Z¹]_a—O—, —S—, —[Z¹—S—]_a—, —[S—Z¹]_a—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR⁸—, C(O)S—, —O(CO)—, —S(CO)—, —NR⁸C(O)— or —NR⁸—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
      • R⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²—C_6-14-aryl,
        • wherein
        • Z² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R⁶ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, —S(O)—, —O(O)—, —C(O)O—, —(CO)NR⁹, —C(O)S—, —O(CO)—, —S(CO)—, —NR⁹C(O)—, —NR⁹—, —Z³—SiR⁹₂—Z⁴—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R⁹ at each occurrence is independently H, C_1-20-alkyl, or —Z⁵—C_6-14-aryl,
        • wherein
        • Z⁵ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar² and Ar³ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^b, wherein each R^b is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X³—Ar⁴, —X³—Ar⁵—Ar⁴, —X³—Ar⁵—R¹⁰, or —X³—Ar⁵—Ar⁶—R¹⁰,
      • wherein
      • X³ at each occurrence is independently —Z⁶—O—Z⁷—, —Z⁶—S—Z⁷, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹¹, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹¹C(O)—, —NR¹¹—, —Z⁶—SiR¹¹₂—Z⁷—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z⁶ and Z⁷ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹¹ at each occurrence is independently H, C_1-20-alkyl or —Z⁸—C_6-14-aryl,
        •  wherein
        •  Z⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar⁴ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^c, wherein each R^c is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar⁵ and Ar⁶ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^d, wherein each R^d is independently selected from the group consisting of halogen, CN, C_1-6-alkoxy and C_1-6-haloalkyl, and
      • R¹⁰ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
  • R³, R⁴ and R⁵ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X⁴—R¹², —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,
    • wherein
    • X⁴ at each occurrence is independently —[Z⁹—O]_b—, —[Z⁹—S—]_b—, —S(O)—, —C(O)—, —C(O)O—, —C(O)NR¹⁴— or C(O)S—,
      • wherein
      • Z⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • b at each occurrence is independently an integer from 1 to 10 and
      • R¹⁴ at each occurrence is independently H, C_1-20-alkyl, or —Z¹⁰—C_6-14-aryl,
        • wherein
        • Z¹⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R¹² at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁵ at each occurrence is independently —Z¹¹—O—Z¹², —Z¹¹—S—Z¹²—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁵, —C(O)S—, —Z¹¹—SiR¹⁵₂—Z¹²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z¹¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • Z¹² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R¹⁵ at each occurrence is independently H, C_1-20-alkyl, or —Z¹³—C_6-14-aryl,
        • wherein
        • Z¹³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
    • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁶—Ar¹⁰, —X⁶—Ar¹¹—Ar¹⁰, —X⁶—Ar¹¹—R¹⁶, or —X⁶—Ar¹¹—Ar¹²—R¹⁷,
      • wherein
      • X⁶ at each occurrence is independently —Z¹⁴—O—Z¹⁵—, —Z¹⁴—S—Z¹⁵, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹⁸C(O)—, —NR¹⁸—,
      • —Z¹⁴—SiR¹⁸₂—Z¹⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z¹⁴ and Z¹⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹⁸ at each occurrence is independently H, C_1-20-alkyl or —Z¹⁶—C_6-14-aryl,
        •  wherein
        •  Z¹⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar¹⁰ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^g, wherein each R^g is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar¹¹ and Ar¹² at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^h, wherein each R^h is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
      • R¹⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
  • R¹⁹ is O or C(CN)₂, and
  • R²⁰ and R²¹ are the same or different and are R²² or CN,
    • wherein R²² has the same meaning as R¹,
• G¹ and G² are the same or different and are phenylene or a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue, which phenylene and monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of halogen, —CN, —NO₂, —OH, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_5-10-cycloalkenyl, —Z¹⁷—C_8-10-cycloalkynyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl),
• —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_mH, —S(O)_m—C_1-20-alkyl, —S(O)₂OH, —S(O)_m—OC_1-20-alkyl, —S(O)_m—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_mNH₂, —S(O)_mNH(C_1-20-alkyl), —S(O)_mN(C_1-20-alkyl)₂, —S(O)_mNH(C_6-14-aryl), —S(O)_mN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_mN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, —S—C_1-20-alkyl, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • m at each occurrence is independently 0, 1 or 2,
• L is C_6-24-arylene or a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein C_6-24-arylene and bivalent 5 to 18 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, OH, *═C(C_1-30-alkyl)₂, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_5-10-cycloalkenyl, —Z¹⁸—C_8-10-cycloalkynyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_oH, —S(O)_o—C_1-20-alkyl, —S(O)₂OH, —S(O)_o—OC_1-20-alkyl, —S(O)_o—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_oNH₂, —S(O)_oNH(C_1-20-alkyl), —S(O)_oN(C_1-20-alkyl)₂, —S(O)_oNH(C_6-14-aryl), —S(O)_oN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_oN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, —S—C_1-20-alkyl, C_1-20-haloalkyl,
• wherein
• Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
• o at each occurrence is independently 0, 1 or 2,or
• L is

• • wherein
  • R²³ and R²⁴ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar¹⁴—R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,
    • wherein
    • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_c—, —[O—Z¹⁹]_c—O—, —S—, —[Z¹⁹—S—]_c—, —[S—Z¹⁹]_c—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR²⁷—, C(O)S—, —O(CO)—, —S(CO)—, —NR²⁷C(O)— or —NR²⁷—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
      • R²⁷ at each occurrence is independently H, C_1-20-alkyl, or —Z²⁰—C_6-14-aryl,
        • wherein
        • Z²⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR²⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR²⁸C(O)—, —NR²⁸—, —Z²¹—SiR²⁸₂—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R²⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²³—C_6-14-aryl,
        • wherein
        • Z²³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹³ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁹—Ar¹⁶, —X⁹—Ar¹⁷—Ar¹⁶, —X⁹—Ar¹⁷—R²⁹, or —X⁹—Ar¹⁷—Ar¹⁸—R²⁹,
      • wherein
      • X⁹ at each occurrence is independently —Z²⁴—O—Z²⁵—, —Z²⁴—S—Z²⁵, —S(O)—, —O(O)—, —C(O)O—, —(CO)NR³⁰, —C(O)S—, —O(CO)—, —S(CO)—, —NR³⁰C(O)—, —NR³⁰—, —Z²⁴—SiR³⁰₂—Z²⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z²⁴ and Z²⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R³⁰ at each occurrence is independently H, C_1-20-alkyl or —Z²⁶—C_6-14-aryl,
        •  wherein
        •  Z²⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar¹⁶ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^q, wherein each R^q is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar¹⁷ and Ar¹⁸ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^r, wherein each R^r is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
      • R²⁹ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
• q and s are the same or different and are 0, 1, 2, 3, 4 or 5,
• r is 0, 1 or 2,and
• n is an integer from 2 to 10'000.

Examples of halogen are —F, —Cl, —Br and —I.

Examples of C_1-6-alkyl are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, neopentyl, isopentyl and n-hexyl. Examples of C_1-20-alkyl are C_1-6-alkyl, n-heptyl, n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀). Examples of C_1-30-alkyl are C_1-20-alkyl, n-docosyl (C₂₂), n-tetracosyl (C₂₄), n-hexacosyl (C₂₆), n-octacosyl (C₂₈) and n-triacontyl (C₃₀).

Examples of C_1-6-haloalkyl are CF₃, CHF₂, CH₂F, C₂F₅, CH₂(CH₂)₄CF₃, CF₃, CCl₃, CHCl₂, CH₂Cl, C₂Cl₅ and CH₂(CH₂)₄CCl₃. Examples of C_1-20-haloalkyl and of C_1-30-haloalkyl are C_1-6-haloalkyl and CH₂(CH₂)₈CF₃, CH₂(CH₂)₁₄CF₃.

Examples of C_1-6-alkoxy are methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy, n-pentoxy, neopentoxy, isopentoxy and n-hexoxy. Examples of C_1-20-alkoxy are C_1-6-alkoxy, n-heptoxy, n-octoxy, n-nonoxy and n-decoxy, n-undecoxy, n-dodoxy, n-undecoxy, n-dodecoxy, n-tridecoxy, n-tetradecoxy, n-pentadecoxy, n-hexadecoxy, n-heptadecoxy, n-octadecoxy, n-nonadecoxy and n-eicosoxy (C₂₀).

Examples of C_2-20-alkenyl are ethenyl, propenyl, cis-2-butenyl, trans-2-butenyl, 3-butenyl, cis-2-pentenyl, trans-2-pentenyl, cis-3-pentenyl, trans-3-pentenyl, 4-pentenyl, 2-methyl-3-butenyl, hexenyl, heptenyl, octenyl, nonenyl, docenyl, undocenyl and oleyl (C₁₈). Examples of C_2-20-alkenyl are also butadienyl, pentadienyl, hexadienyl, linoleyl (C₁₈), linolenyl (C₁₈) and arachidonyl (C₂₀). Examples of C_2-30-alkenyl are C_2-20-alkenyl and erucyl (C₂₂).

Examples of C_2-20-alkynyl are ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl, undecynyl, dodecynyl, undecynyl, dodecynyl, tridecynyl, tetradecynyl, pentadecynyl, hexadecynyl, heptadecynyl, octadecynyl, nonadecynyl and icosynyl (C₂₀). Examples of C_2-30-alkynyl are C_2-20-alkynyl.

Examples of C_3-10-cycloalkyl are preferably monocyclic C_3-10-cycloalkyls such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl, but include also polycyclic C_3-10-cycloalkyls such as decalinyl, norbornyl and adamantyl.

Examples of C_5-10-cycloalkenyl are preferably monocyclic C_5-10-cycloalkenyls such as cyclopentenyl, cyclohexenyl, cyclohexadienyl and cycloheptatrienyl, but include also polycyclic C_5-10-cycloalkenyls.

An example of C_8-10-cycloalkynyl is cyclooctynyl.

The monovalent 3 to 12 membered aliphatic heterocyclic residues can be monocyclic monovalent 3 to 8 membered aliphatic heterocyclic residues or polycyclic, for example bicyclic, monovalent 7 to 12 membered aliphatic heterocyclic residues.

Examples of monocyclic monovalent 3 to 8 membered aliphatic heterocyclic residues are monocyclic monovalent 5 membered aliphatic heterocyclic residues containing one heteroatom such as pyrrolidinyl, 1-pyrrolinyl, 2-pyrrolinyl, 3-pyrrolinyl, tetrahydrofuryl, 2,3-dihydrofuryl, tetrahydrothiophenyl and 2,3-dihydrothiophenyl, monocyclic monovalent 5 membered aliphatic heterocyclic residues containing two heteroatoms such as imidazolidinyl, imidazolinyl, pyrazolidinyl, pyrazolinyl, oxazolidinyl, oxazolinyl, isoxazolidinyl, isoxazolinyl, thiazolidinyl, thiazolinyl, isothiazolidinyl and isothiazolinyl, monocyclic monovalent 5 membered aliphatic heterocyclic residues containing three heteroatoms such as 1,2,3-triazolyl, 1,2,4-triazolyl and 1,4,2-dithiazolyl, monocyclic monovalent 6 membered aliphatic heterocyclic residues containing one heteroatom such as piperidyl, piperidino, tetrahydropyranyl, pyranyl, thianyl and thiopyranyl, monocyclic monovalent 6 membered aliphatic heterocyclic residues containing two heteroatoms such as piperazinyl, morpholinyl and morpholino and thiazinyl, monocyclic monovalent 7 membered aliphatic heterocyclic residues containing one hereoatom such as azepanyl, azepinyl, oxepanyl, thiepanyl, thiapanyl, thiepinyl, and monocyclic monovalent 7 membered aliphatic heterocyclic residues containing two hereoatom such as 1,2-diazepinyl and 1,3-thiazepinyl.

The monovalent 3 to 12 membered aliphatic heterocyclic residues can contain one or more heteroatoms, which can independently be selected from the group consisting of nitrogen, oxygen, sulfur, phosphor, silicon and arsenic, preferably from the group consisting of nitrogen, oxygen and sulfur.

Examples of monocyclic monovalent 3 to 12 membered aliphatic heterocyclic residue substituted with *═O are 2-oxazolidonyl, 4-piperidonyl, 4-piperidono, pyrimidine-2,4(1H,3H)-dionyl and 2-pyridonyl.

An example of a bicyclic monovalent 7 to 12 membered aliphatic heterocyclic residue is decahydronaphthyl.

C_6-14-aryl can be monocyclic or polycyclic. Examples of C_6-14-aryl are monocyclic C₆-aryl such as phenyl, bicyclic C_9-10-aryl such as 1-naphthyl, 2-naphthyl, indenyl, indanyl and tetrahydronaphthyl, and tricyclic C_12-14-aryl such as anthryl, phenanthryl, fluorenyl and s-indacenyl.

C_6-14-haloaryl can be monocyclic or polycyclic. Examples of C_6-14-haloaryl are 6-chlorophenyl and 2-chlorophenyl.

The monovalent 5 to 14 membered aromatic heterocyclic residues can be monocyclic monovalent 5 to 8 membered aromatic heterocyclic residues, or polycyclic monovalent 7 to 12 membered aromatic heterocyclic residues, for example bicyclic or tricyclic monovalent 9 to 14 membered aromatic heterocyclic residues.

Examples of monocyclic monovalent 5 to 8 membered aromatic heterocyclic residues are monocyclic monovalent 5 membered aromatic heterocyclic residues containing one heteroatom such as pyrrolyl, furyl and thiophenyl, monocyclic monovalent 5 membered aromatic heterocyclic residues containing two heteroatoms such as imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, monocyclic monovalent 5 membered aromatic heterocyclic residues containing three heteroatoms such as 1,2,3-triazolyl, 1,2,4-triazolyl and oxadiazolyl, monocyclic monovalent 5 membered aromatic heterocyclic residues containing four heteroatoms such as tetrazolyl, monocyclic monovalent 6 membered aromatic heterocyclic residues containing one heteroatom such as pyridyl, monocyclic monovalent 6 membered aromatic heterocyclic residues containing two heteroatoms such as pyrazinyl, pyrimidinyl and pyridazinyl, monocyclic monovalent 6 membered aromatic heterocyclic residues containing three heteroatoms such as 1,2,3-triazinyl, 1,2,4-triazinyl and 1,3,5-triazinyl, monocyclic monovalent 7 membered aromatic heterocyclic residues containing one heteroatom such as azepinyl, and monocyclic monovalent 7 membered aromatic heterocyclic residues containing two heteroatoms such as 1,2-diazepinyl,

Examples of bicyclic monovalent 7 to 12 membered aromatic heterocyclic residues are bicyclic 9 membered aromatic heterocyclic residues containing one heteroatom such as indolyl, isoindolyl, indolizinyl, indolinyl, benzofuryl, isobenzofuryl, benzothiophenyl and isobenzothiophenyl, bicyclic monovalent 9 membered aromatic heterocyclic residues containing two heteroatoms such as indazolyl, benzimidazolyl, benzimidazolinyl, benzoxazolyl, benzisooxazolyl, benzthiazolyl, benzisothiazolyl, furopyridyl and thienopyridyl, bicyclic monovalent 9 membered aromatic heterocyclic residues containing three heteroatoms such as benzotriazolyl, benzoxadiazolyl, oxazolopyridyl, isooxazolopyridyl, thiazolopyridyl, isothiazolopyridyl and imidazopyridyl, bicyclic monovalent 9 membered aromatic heterocyclic residues containing four heteroatoms such as purinyl, bicyclic monovalent 10 membered aromatic heterocyclic residues containing one heteroatom such as quinolyl, isoquinolyl, chromenyl and chromanyl, bicyclic monovalent 10 membered aromatic heterocyclic residues containing two heteroatoms such as quinoxalinyl, quinazolinyl, cinnolinyl, phthalazinyl, 1,5-naphthyridinyl and 1,8-naphthyridinyl, bicyclic monovalent 10 membered aromatic heterocyclic residues containing three heteroatoms such as pyridopyrazinyl, pyridopyrimidinyl and pyridopyridazinyl, and bicyclic monovalent 10 membered aromatic heterocyclic residues containing four heteroatoms such as pteridinyl.

Examples of tricyclic monovalent 9 to 14 membered aromatic heterocyclic residues are dibenzofuryl, acridinyl, phenoxazinyl, 7H-cyclopenta[1,2-b:3,4-b′]dithiophenyl and 4H-cyclopenta[2,1-b:3,4-b′]dithiophenyl.

The monovalent 5 to 14 membered aromatic heterocyclic residue can contain one or more heteroatoms which can independently be selected from the group consisting of nitrogen, oxygen, sulfur, phosphor, silicon and arsenic, preferably from the group consisting of nitrogen, oxygen and sulfur.

Examples of C_1-6-alkylene are methylene, ethylene, butylene, pentylene, hexylene and 2-methylpentylene. Examples of C_1-30-alkylene are C_1-6-alkylene, CH₂(CH₂)₁₀)CH₂ and CH₂(CH₂)₂₀)CH₂.

Examples of C_2-6-alkenylene are ethenylene, cis-2-butenylene, trans-butenylene, cis-2-pentenylene, trans-2-pentenylene, trans-2-hexenylene, trans-3-hexenylene and 2-methyl-trans-3-pentenylene. Examples of C_2-30-alkenylene are C_2-6-alkenylene, CH₂(CH₂)₄—CH═CH—(CH₂)₄CH₂ and CH₂(CH₂)₉—CH═CH—(CH₂)₉CH₂.

Examples of C_1-6-haloalkylene are CF₂, CCl₂, CF₂CF₂, CCl₂CCl₂, CHFCH₂, CHFCH₂CH₂CHF and CHF(CH₂)₄CHF. Examples of C_1-30-haloalkylene are C_1-6-haloalkylene, CHF(CH₂)₁₀CHF and CHF(CH₂)₂₀CHF.

Examples of C_6-14-arylene are monocyclic C₆-arylene such as phenylene, bicyclic C_9-10-arylene such as 1-naphthylene, 2-naphthyl, indenylene, indanylene and tetrahydronaphthylene, and tricyclic C_12-14-arylene such as anthrylene, phenanthrylene, fluorenylene and s-indacenylene. Examples of C_6-24-arylene are C_6-14-arylene and pyrenylene, tetracenylene, perylenylene, indenofluorenylene, pentacenylene, coronenylene and tetraphenylenylene.

The bivalent 5 to 14 membered aromatic heterocyclic residues can be monocyclic bivalent 5 to 8 membered aromatic heterocyclic residues, or polycyclic bivalent 7 to 12 membered aromatic heterocyclic residues, for example bicyclic or tricyclic bivalent 9 to 14 membered aromatic heterocyclic residues.

Examples of monocyclic bivalent 5 to 8 membered aromatic heterocyclic residues are monocyclic bivalent 5 membered aromatic heterocyclic residues containing one heteroatom such as pyrrolylene, furylene and thiophenylene, monocyclic bivalent 5 membered aromatic heterocyclic residues containing two heteroatoms such as imidazolylene, pyrazolylene, oxazolylene, isoxazolylene, thiazolylene, isothiazolylene, monocyclic bivalent 5 membered aromatic heterocyclic residues containing three heteroatoms such as 1,2,3-triazolylene, 1,2,4-triazolylene and oxadiazolylene, monocyclic bivalent 5 membered aromatic heterocyclic residues containing four heteroatoms such as tetrazolylene, monocyclic bivalent 6 membered aromatic heterocyclic residues containing one heteroatom such as pyridylene, monocyclic bivalent 6 membered aromatic heterocyclic residues containing two heteroatoms such as pyrazinylene, pyrimidinylene and pyridazinylene, monocyclic bivalent 6 membered aromatic heterocyclic residues containing three heteroatoms such as 1,2,3-triazinylene, 1,2,4-triazinylene and 1,3,5-triazinylene, monocyclic bivalent 7 membered aromatic heterocyclic residues containing one heteroatom such as azepinylene, and monocyclic bivalent 7 membered aromatic heterocyclic residues containing two heteroatoms such as 1,2-diazepinylene.

Examples of bicyclic bivalent 7 to 12 membered aromatic heterocyclic residues are bicyclic bivalent 9 membered aromatic heterocyclic residues containing one heteroatom such as indolylene, isoindolylene, indolizinylene, indolinylene, benzofurylene, isobenzofurylene, benzothiophenylene and isobenzothiophenylene, bicyclic bivalent 9 membered aromatic heterocyclic residues containing two heteroatoms such as indazolylene, benzimidazolylene, benzimidazolinylene, benzoxazolylene, benzisooxazolylene, benzthiazolylene, benzisothiazolylene, furopyridylene and thienopyridylene, bicyclic bivalent 9 membered aromatic heterocyclic residues containing three heteroatoms such as benzotriazolylene, benzoxadiazolylene, oxazolopyridylene, isooxazolopyridylene, thiazolopyridylene, isothiazolopyridylene and imidazopyridylene, bicyclic bivalent 9 membered aromatic heterocyclic residues containing four heteroatoms such as purinylene, bicyclic bivalent 10 membered aromatic heterocyclic residues containing one heteroatom such as quinolylene, isoquinolylene, chromenylene and chromanylene, bicyclic bivalent 10 membered aromatic heterocyclic residues containing two heteroatoms such as quinoxalinylene, quinazolinylene, cinnolinylene, phthalazinylene, 1,5-naphthyridinylene and 1,8-naphthyridinylene, bicyclic bivalent 10 membered aromatic heterocyclic residues containing three heteroatoms such as pyridopyrazinylene, pyridopyrimidinylene and pyridopyridazinylene, and bicyclic bivalent 10 membered aromatic heterocyclic residues containing four heteroatoms such as pteridinylene.

Examples of tricyclic bivalent 9 to 14 membered aromatic heterocyclic residues containing one heteroatom are dibenzofurylene and acridinylene. Examples of a tricyclic bivalent 9 to 14 membered aromatic heterocyclic residues containing two heteroatoms are phenoxazinylene, 7H-cyclopenta[1,2-b:3,4-b′]dithiophenylene and 4H-cyclopenta[2,1-b:3,4-b′]dithiophenylene.

Examples of bivalent 5 to 18 membered aromatic heterocyclic residues are bivalent 5 to 14 membered aromatic heterocyclic residues.

The bivalent 5 to 14 membered, respectively, 5 to 18 membered aromatic heterocyclic residue can contain one or more heteroatoms which can independently be selected from the group consisting of nitrogen, oxygen, sulfur, phosphor, silicon and arsenic, preferably from the group consisting of nitrogen, silicon and sulfur.

Preferably, A¹ and A² are S.

Preferably, E is selected from the group consisting of

More preferably, E is selected from the group consisting of

Most preferably, E is

Preferably, R¹ and R² are the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X¹—R⁶, —X²—Ar¹, —X²—Ar²—Ar¹, —X²—Ar²—R⁷ or —X²—Ar²—Ar³—R⁷,

• • wherein
  • X¹ at each occurrence is independently —O—, —[Z¹—O]_a—, —[O—Z¹]_a—O—, —S—, —[Z¹—S—]_a—, —[S—Z¹]_a—S—, —S(O), —C(O)—, —C(O)O—, —C(O)—NR⁸—, C(O)S—, —O(CO)—, —S(CO)—, —NR⁸C(O)— or —NR⁸—,
    • wherein
    • Z¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • a at each occurrence is independently an integer from 1 to 10 and
    • R⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²—C_6-14-aryl,
      • wherein
      • Z² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
  • R⁶ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR⁹, —C(O)S—, —O(CO)—, —S(CO)—, —NR⁹C(O)—, —NR⁹—, —Z³—SiR⁹₂—Z⁴—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
    • R⁹ at each occurrence is independently H, C_1-20-alkyl, or —Z⁵—C_6-14-aryl,
      • wherein
      • Z⁵ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
  • Ar¹ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar² and Ar³ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^b, wherein each R^b is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
  • R⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl and C_1-20-alkoxy.

More preferably, R¹ and R² are the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X¹—R⁶, —X²—Ar¹, —X²—Ar²—Ar¹, —X²—Ar²—R⁷ or —X²—Ar²—Ar³—R⁷,

• • wherein
  • X¹ at each occurrence is independently —O—, —[Z¹—O]_a—, —[O—Z¹]_a—O—, —S—, —[Z¹—S—]_a—, or
    • wherein
    • Z¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • a at each occurrence is independently an integer from 1 to 10 and
  • R⁶ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • Ar¹ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar² and Ar³ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^b, wherein each R^b is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
  • R⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy.

Even more preferably, R¹ and R² are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X¹—R⁶ or —X²—Ar¹,

• • wherein
  • X¹ at each occurrence is independently —[Z¹—O]_a—, —[Z¹—S—]_a—, or —[S—Z¹]_a—S—,
    • wherein
    • Z¹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
    • a at each occurrence is independently an integer from 1 to 10 and
  • R⁶ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
  • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, C_1-30-alkylene or C_1-30-haloalkylene,
    • wherein
    • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
  • Ar¹ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

Most preferably, R¹ and R² are the same or different and are C_1-30-alkyl, C_1-30-haloalkyl or —X²—Ar¹,

• • wherein
  • X² at each occurrence is independently C_1-30-alkylene or C_1-30-haloalkylene, and
  • Ar¹ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

In particular, R¹ and R² are the same or different and are C_1-30-alkyl, for example C_1-20-alkyl or C_1-6-alkyl, for example methyl or n-hexyl.

Preferably, R³ is H, halogen, CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X⁴—R¹², —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,

• • wherein
  • X⁴ at each occurrence is independently —[Z⁹—O]_b—, —[Z⁹—S—]_b—, —S(O)—, —C(O)—, —C(O)O—, —C(O)NR¹⁴— or C(O)S—,
    • wherein
    • Z⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • b at each occurrence is independently an integer from 1 to 10 and
    • R¹⁴ at each occurrence is independently H, C_1-20-alkyl, or —Z¹⁰—C_6-14-aryl,
      • wherein
      • Z¹⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
  • R¹² at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X⁵ at each occurrence is independently —Z¹¹—O—Z¹², —Z¹¹—S—Z¹²—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁵, —C(O)S—, —Z¹¹—SiR¹⁵₂—Z¹²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z¹¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • Z¹² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
    • R¹⁵ at each occurrence is independently H, C_1-20-alkyl, or —Z¹³—C_6-14-aryl,
      • wherein
      • Z¹³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
  • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
  • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,

More preferably, R³ is H, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X⁴—R¹², —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,

• • wherein
  • X⁴ at each occurrence is independently —[Z⁹—O]_b— or —[Z⁹—S—]_b—,
    • wherein
    • Z⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene, and
    • b at each occurrence is independently an integer from 1 to 10 and
  • R¹² at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X⁵ at each occurrence is independently —Z¹¹—O—Z¹²—, —Z¹¹—S—Z¹²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z¹¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene, and
    • Z¹² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and

R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy.

Most preferably, R³ is —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,

• • wherein
  • X⁵ at each occurrence is a covalent bond,
  • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
  • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy.

In particular, R³ is —X⁵—Ar⁸—R¹³,

• • wherein
  • X⁵ is a covalent bond,
  • Ar⁸ is C_6-14-arylene, for example phenylene, and
  • R¹³ is C_1-20-alkyl.

For example R³ is

Preferably, G¹ and G² are the same or different and are phenylene, such as

or, preferably, a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue selected from the group consisting of

• • wherein
  • M¹ is S, O, NH or SiR^sR^s, preferably M¹ is S or NH, more preferably M¹ is S,
    • wherein R^s is hydrogen or C_1-30-alkyl,
• which phenylene or monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 2 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of —CN, C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN, *═O, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_m—C_1-20-alkyl, —S(O)_m—OC_1-20-alkyl, —S(O)_m—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_mNH₂, —S(O)_mNH(C_1-20-alkyl), —S(O)_mN(C_1-20-alkyl)₂, —S(O)_mNH(C_6-14-aryl), —S(O)_mN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_mN(C_6-14-aryl)₂ and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond, and
  • m at each occurrence is independently 0, 1 or 2.

Preferably, each Rⁱ is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond.

More preferably, each Rⁱ is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁷—C_6-14-aryl,

• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O,
  • wherein
  • Z¹⁷ at each occurrence is a covalent bond and
  • C_6-14-aryl is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy.

Most preferably, each Rⁱ is independently C_1-30-alkyl, preferably n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀), more preferably, n-dodecyl.

More preferably, G¹ and G² are the same or different and are phenylene, such as

or, preferably, a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue selected from the group consisting of

• which phenylene or monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 2 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond.

Most preferably, G¹ and G² are the same or different and are a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue which monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue is

• which monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue is substituted with 1 to 2 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁷—C_6-14-aryl,
• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_6-14-aryl is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy,
  • wherein
  • Z¹⁷ at each occurrence is a covalent bond.

In particular, G¹ and G² are the same or different and are a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue which monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue is

• which monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue is substituted with 1 substituents Rⁱ, wherein Rⁱ is C_1-30-alkyl, preferably n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀), more preferably, n-dodecyl.

Preferably, L is C_6-24-arylene or a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein C_6-24-arylene and bivalent 5 to 18 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of —CN, C_1-30-alkyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_3-30-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN, *═O, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_o—C_1-20-alkyl, —S(O)_o—OC_1-20-alkyl, —S(O)_o—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_oNH₂, —S(O)_oNH(C_1-20-alkyl), —S(O)_oN(C_1-20-alkyl)₂, —S(O)_oNH(C_6-14-aryl), —S(O)_oN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_oN(C_6-14-aryl)₂ and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, —S—C_1-20-alkyl, C_1-20-haloalkyl,
  • wherein
  • Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond, and
  • o at each occurrence is independently 0, 1 or 2,or
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar¹⁴—R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,
    • wherein
    • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_o—, —[O—Z¹⁹]_o—O—, —S—, —[Z¹⁹—S—]_o—, —[S—Z¹⁹]_o—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR²⁷—, C(O)S—, —O(CO)—, —S(CO)—, —NR²⁷C(O)— or —NR²⁷—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
      • R²⁷ at each occurrence is independently H, C_1-20-alkyl, or —Z²⁰—C_6-14-aryl,
        • wherein
        • Z²⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR²⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR²⁸C(O)—, —NR²⁸—, —Z²¹—SiR²⁸₂—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R²⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²³—C_6-14-aryl,
        • wherein
        • Z²³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹⁴ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl and C_1-20-alkoxy.

Preferably, each R^l is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-30-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁶ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond.

More preferably, each R^l is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁸—C_6-14-aryl,

• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_6-14-aryl is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy,
  • wherein
  • Z¹⁸ at each occurrence is a covalent bond.

Most preferably, each R^l is independently C_1-30-alkyl, preferably n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀), more preferably, n-hexadecyl.

Preferably, R²³ and R²⁴ are the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar¹⁴—R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,

• • wherein
  • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_c—, —[O—Z¹⁹]_c—O—, —S—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
    • wherein
    • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • c at each occurrence is independently an integer from 1 to 10 and
  • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • Ar¹³ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
  • Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
  • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy.

More preferably, R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁸—Ar¹³,

• • wherein
  • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
    • wherein
    • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
    • c at each occurrence is independently an integer from 1 to 10 and
  • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
  • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
    • wherein
    • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
  • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

Most preferably, R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl or C_1-30-haloalkyl, in particular H.

More preferably, L is a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond,or
• L is

wherein

• R²³ and R²⁴ are the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_1-30-haloalkyl, —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar¹⁴—R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,
  • wherein
  • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_c—, —[O—Z¹⁹]_c—O—, —S—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
    • wherein
    • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
    • c at each occurrence is independently an integer from 1 to 10 and
  • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
  • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
    • wherein
    • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • Ar¹³ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,

Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and

• • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy.

Even more preferably, L is a bivalent 5 to 18 membered aromatic heterocyclic residue selected from the group consisting of

• wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^l, wherein each R^l R^l is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁸—C_6-14-aryl,
• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_6-14-aryl is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy,
  • wherein
  • Z¹⁸ at each occurrence is a covalent bond,
  • wherein,
  • M¹, M² and M³ can be the same or different and are S, O, NH or SiR^tR^t, preferably M¹, M² are S or NH, and M³ is S, O, NH or SiR^tR^t, more preferably M¹ and M² are S, and M³ is NH or SiR^tR^t,
    • wherein R^t is H or C_1-30-alkyl,or
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁸—Ar¹³,
    • wherein
    • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
    • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

Even more preferably,

• L is a bivalent 5 to 18 membered aromatic heterocyclic residue selected from the group consisting of

• wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^l, wherein each wherein each R^l R^l is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁸—C_6-14-aryl,
• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_6-14-aryl is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy,
  • wherein
  • Z¹⁸ at each occurrence is a covalent bond,
  • wherein R¹ is hydrogen or C_1-30-alkyl,or
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁸—Ar¹³,
    • wherein
    • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
    • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

Even more preferably,

• L is a bivalent 5 to 18 membered aromatic heterocyclic residue selected from the group consisting of

• wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^l, wherein each R^l R^l is independently selected from the group consisting of C_1-30-alkyl and —Z¹⁸—C_6-14-aryl,
• wherein C_1-30-alkyl and C_6-14-aryl are optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_6-14-aryl is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl and C_1-20-alkoxy,
  • wherein
  • Z¹⁸ at each occurrence is a covalent bond,
  • wherein R¹ is hydrogen or C_1-30-alkyl,or
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁸—Ar¹³,
    • wherein
    • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
    • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

Most preferably,

• L is

• wherein each R^l is independently C_1-30-alkyl, preferably n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀), more preferably, n-hexadecyl,or
• L is

wherein

• R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl or C_1-30-haloalkyl, in particular H.

Preferably, q, r and s are 0 or 1, with the proviso that q, r and s are not all 0 at the same time.

Preferably, n is an integer from 1 to 5000, 1 to 1000, 1 to 100, 1 to 50 or from 1 to 30, for example n can be an integer from 2 to 5000, 2 to 1000, 2 to 50, 2 to 30. In some embodiments, n can be an integer from 4 to 1000, 4 to 100, 8 to 1000 or 8 to 100.

In one embodiment,

• A¹ and A² are S,
• E is

• • wherein
  • R¹ and R² are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X¹—R⁶ or —X²—Ar¹,
    • wherein
    • X¹ at each occurrence is independently —[Z¹—O]_a—, —[Z¹—S—]_a—, or —[S—Z¹]_a—S—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
    • R⁶ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy.

L is a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—S—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond,
• q and s are 0,
• r is 1,and
• n is an integer from 1 to 1000, preferably 4 to 100.

In a second embodiment,

• A¹ and A² are S,
• E is

• • wherein
  • R¹ and R² are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X¹—R⁶ or —X²—Ar¹,
    • wherein
    • X¹ at each occurrence is independently —[Z¹—O]_a—, —[Z¹—S—]_a—, or —[S—Z¹]_a—S—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
    • R⁶ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy,
• G¹ and G² are the same or different and are phenylene such as

or, preferably, a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue selected from the group consisting of

• which phenylene or monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 2 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30 alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond.
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁵—Ar¹³,
    • wherein
    • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
    • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy,
• q and s are 1,
• r is 1,and
• n is an integer from 1 to 1000, preferably from 2 to 50.

In a third embodiment,

• A¹ and A² are S,
• E is

• • wherein
  • R¹ and R² are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X¹—R⁶ or —X²—Ar¹,
    • wherein
    • X¹ at each occurrence is independently —[Z¹—O]_a—, —[Z¹—S—]_a—, or —[S—Z¹]_a—S—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
    • R⁶ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy,
• G¹ and G² are the same or different and are phenylene such as

or, preferably, a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue selected from the group consisting of

• which phenylene or monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 2 substituents Rⁱ wherein each Rⁱ is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-30-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond,
• q and s are 1,
• r is 0,and
• n is an integer from 1 to 1000, preferably from 1 to 30.

In a fourth embodiment,

• A¹ and A² are S,
• E is

• • wherein
  • R³ is —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,
    • wherein
    • X⁵ at each occurrence is a covalent bond,
    • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
  • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
• G¹ and G² are the same or different and are phenylene such as

or, preferably, a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue selected from the group consisting of

• which phenylene or monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 2 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of C_1-30-alkyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN and *═O, and
• wherein C_3-10-cycloalkyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_1-6-haloalkylene or a covalent bond,
• L is

• • wherein
  • R²³ and R²⁴ are the same or different and are H, C_1-30-alkyl, C_1-30-haloalkyl, —X⁷—R²⁵ or —X⁸—Ar¹³,
    • wherein
    • X⁷ at each occurrence is independently —[Z¹⁹—O]_c—, —[Z¹⁹—S—]_c—, or —[S—Z¹⁹]_c—S—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
    • R²⁵ at each occurrence is independently C_1-30-alkyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, C_1-30-alkylene or C_1-30-haloalkylene,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene or C_1-6-haloalkylene, and
    • Ar¹³ at each occurrence is independently C_6-14-aryl, optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen C_1-6-alkyl and C_1-6-alkoxy,
• q and s are 1,
• r is 1,and
• n is an integer from 1 to 1000, preferably from 2 to 50.

Examples of compounds, oligomers or polymers of formula 1 are

• wherein n is an integer from 1 to 1000, preferably 1 to 100, 1 to 50 or from 1 to 30, for example n can be an integer from 2 to 1000, 2 to 100, 2 to 50, 2 to 30, or an integer from 4 to 100 or 8 to 100.

Also part of the present invention is a process for the preparation of the compound, oligomer or polymer of formula

wherein

• A¹ and A² can be the same or different and are S or Se,
• E is selected from the group consisting of

• • wherein
  • R¹ and R² can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X¹—R⁶, —X²—Ar¹, —X²—Ar²—Ar¹, —X²—Ar²—R⁷ or —X²—Ar²—Ar³—R⁷,
    • wherein
    • X¹ at each occurrence is independently —O—, —[Z¹—O]_a—, —[O—Z¹]_a—O—, —S—, —[Z¹—S—]_a—, —[S—Z¹]_a—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR⁸—, C(O)S—, —O(CO)—, —S(CO)—, —NR⁸C(O)— or —NR⁸—,
      • wherein
      • Z¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • a at each occurrence is independently an integer from 1 to 10 and
      • R⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²—C_6-14-aryl,
        • wherein
        • Z² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R⁶ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X² at each occurrence is independently —Z³—O—Z⁴—, —Z³—S—Z⁴—, —S(O)—, —O(O)—, —C(O)O—, —(CO)NR⁹, —C(O)S—, —O(CO)—, —S(CO)—, —NR⁹C(O)—, —NR⁹—, —Z³—SiR⁹₂—Z⁴—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z³ and Z⁴ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R⁹ at each occurrence is independently H, C_1-20-alkyl, or —Z⁵—C_6-14-aryl,
        • wherein
        • Z⁵ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^a, wherein each R^a is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar² and Ar³ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^b, wherein each R^b is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X³—Ar⁴, —X³—Ar⁵—Ar⁴, —X³—Ar⁵—R¹⁰, or —X³—Ar⁵—Ar⁶—R¹⁰,
      • wherein
      • X³ at each occurrence is independently —Z⁶—O—Z⁷—, —Z⁶—S—Z⁷, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹¹, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹¹C(O)—, —NR¹¹—, —Z⁶—SiR¹¹₂—Z⁷—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z⁶ and Z⁷ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹¹ at each occurrence is independently H, C_1-20-alkyl or —Z⁸—C_6-14-aryl,
        •  wherein
        •  Z⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
      • Ar⁴ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^c, wherein each R^c is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
      • Ar⁵ and Ar⁶ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^d, wherein each R^d is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
      • R¹⁰ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
  • R³, R⁴ and R⁵ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X⁴—R¹², —X⁵—Ar⁷, —X⁵—Ar⁸—Ar⁷, —X⁵—Ar⁸—R¹³ or —X⁵—Ar⁸—Ar⁹—R¹³,
    • wherein
    • X⁴ at each occurrence is independently —[Z⁹—O]_b—, —[Z⁹—S—]_b—, —S(O)—, —C(O)—, —C(O)O—, —C(O)NR¹⁴— or C(O)S—,
      • wherein
      • Z⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • b at each occurrence is independently an integer from 1 to 10 and
      • R¹⁴ at each occurrence is independently H, C_1-20-alkyl, or —Z¹⁰—C_6-14-aryl,
        • wherein
        • Z¹⁰ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R¹² at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁵ at each occurrence is independently —Z¹¹—O—Z¹², —Z¹¹—S—Z¹²—, —S(O)—, —O(O)—, —C(O)O—, —(CO)NR¹⁵, —C(O)S—, —Z¹¹—SiR¹⁵₂—Z¹²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z¹¹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • Z¹² at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R¹⁵ at each occurrence is independently H, C_1-20-alkyl, or —Z¹³—C_6-14-aryl,
        • wherein
        • Z¹³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar⁷ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^e, wherein each R^e is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar⁸ and Ar⁹ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^f, wherein each R^f is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
    • R¹³ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁶—Ar¹⁰, —X⁶—Ar¹¹—Ar¹⁰, —X⁶—Ar¹¹—R¹⁶, or —X⁶—Ar¹¹—Ar¹²—R¹⁷,
      • wherein
      • X⁶ at each occurrence is independently —Z¹⁴—O—Z¹⁵—, —Z¹⁴—S—Z¹⁵, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR¹⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR¹⁸C(O)—, —NR¹⁸—,
      • —Z¹⁴—SiR¹⁸₂—Z¹⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z¹⁴ and Z¹⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R¹⁸ at each occurrence is independently H, C_1-20-alkyl or —Z¹⁶—C_6-14-aryl,
        •  wherein
        •  Z¹⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹⁰ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^g, wherein each R^g is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹¹ and Ar¹² at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^h, wherein each R^h is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl and
    • R¹⁷ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
  • R¹⁹ is O or C(CN)₂, and
  • R²⁰ and R²¹ are the same or different and are R²² or CN,
  • wherein R²² has the same meaning as R¹,

G¹ and G² are the same or different and are phenylene or a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue, which phenylene and monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents Rⁱ, wherein each Rⁱ is independently selected from the group consisting of halogen, —CN, —NO₂, OH, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁷—O—C_1-30-alkyl, —Z¹⁷—S—C_1-30-alkyl, —Z¹⁷—C_3-10-cycloalkyl, —Z¹⁷—C_5-10-cycloalkenyl, —Z¹⁷—C_8-10-cycloalkynyl, —Z¹⁷—C_6-14-aryl, —Z¹⁷-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁷-monovalent 5 to 14 membered aromatic heterocyclic residue,

• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-30-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^j, wherein each R^j is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)—C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_mH, —S(O)_m—C_1-20-alkyl, —S(O)₂OH, —S(O)_m—OC_1-20-alkyl, —S(O)_m—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_mNH₂, —S(O)_mNH(C_1-20-alkyl), —S(O)_mN(C_1-20-alkyl)₂, —S(O)_mNH(C_6-14-aryl), —S(O)_mN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_mN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-10-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^k, wherein each R^k is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, —S—C_1-20-alkyl, C_1-20-haloalkyl,
  • wherein
  • Z¹⁷ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • m at each occurrence is independently 0, 1 or 2,
• L is C_6-24-arylene or a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein C_6-24-arylene and bivalent 5 to 18 membered aromatic heterocyclic residue are optionally substituted with 1 to 4 substituents R^l, wherein each R^l is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, OH, *═C(C_1-30-alkyl)₂, C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, —Z¹⁸—O—C_1-30-alkyl, —Z¹⁸—C_3-10-cycloalkyl, —Z¹⁸—C_5-10-cycloalkenyl, —Z¹⁸—C_8-10-cycloalkynyl, —Z¹⁸—C_6-14-aryl, —Z¹⁸-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z¹⁸-monovalent 5 to 14 membered aromatic heterocyclic residue,
• wherein C_1-30-alkyl, C_2-30-alkenyl, C_2-30-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents R^m, wherein each R^m is independently selected from the group consisting of halogen, —CN, —NO₂, *═O, —OH, —NH₂, —NH(C_1-20-alkyl), —N(C_1-20-alkyl)₂, —N(C_1-20-alkyl)-C_6-14-aryl, —N(C_6-14-aryl)₂, —S(O)_oH, —S(O)_o—C_1-20-alkyl, —S(O)₂OH, —S(O)_o—OC_1-20-alkyl, —S(O)_o—OC_6-14-aryl, —CHO, —C(O)—C_1-20-alkyl, —C(O)—C_6-14-aryl, —C(O)OH, —C(O)—OC_1-20-alkyl, —C(O)—OC_6-14-aryl, —C(O)NH₂, —C(O)NH—C_1-20-alkyl, —C(O)N(C_1-20-alkyl)₂, —C(O)NH—C_6-14-aryl, —C(O)N(C_1-20-alkyl)-C_6-14-aryl, —C(O)N(C_6-14-aryl)₂, —C(S)NH₂, —C(S)NH—C_1-20-alkyl, —C(S)N(C_1-20-alkyl)₂, —C(S)N(C_6-14-aryl)₂, —C(S)N(C_1-20-alkyl)-C_6-14-aryl, —C(S)NH—C_6-14-aryl, —S(O)_oNH₂, —S(O)_oNH(C_1-20-alkyl), —S(O)_oN(C_1-20-alkyl)₂, —S(O)_oNH(C_6-14-aryl), —S(O)_oN(C_1-20-alkyl)-C_6-14-aryl, —S(O)_oN(C_6-14-aryl)₂, SiH₃, SiH(C_1-20-alkyl)₂, SiH₂(C_1-20-alkyl) and Si(C_1-20-alkyl)₃, and
• wherein C_3-30-cycloalkyl, C_5-10-cycloalkenyl, —C_8-10-cycloalkynyl, C_6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rⁿ, wherein each Rⁿ is independently selected from the group consisting of C_1-20-alkyl, C_2-20-alkenyl, C_2-20-alkynyl, C_1-20-alkoxy, C_1-20-haloalkyl,
  • wherein
  • Z¹⁸ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
  • o at each occurrence is independently 0, 1 or 2,or
• L is

• • wherein
  • R²³ and R²⁴ can be the same or different and are H, halogen, —CN, C_1-30-alkyl, C_2-30-alkenyl, C_2-20-alkynyl, C_3-10-cycloalkyl, C_5-10-cycloalkenyl, C_8-10-cycloalkynyl, C_1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue,
  • —X⁷—R²⁵, —X⁸—Ar¹³, —X⁸—Ar¹⁴—Ar¹³, —X⁸—Ar^14-R²⁶ or —X⁸—Ar¹⁴—Ar¹⁵—R²⁶,
    • wherein
    • X⁷ at each occurrence is independently —O—, —[Z¹⁹—O]_c—, —[O—Z¹⁹]_c—O—, —S—, —[Z¹⁹—S—]_c—, —[S—Z¹⁹]_c—S—, —S(O), —C(O)—, —C(O)O—, —C(O)NR²⁷—, C(O)S—, —O(CO)—, —S(CO)—, —NR²⁷C(O)— or —NR²⁷—,
      • wherein
      • Z¹⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene or C_1-6-haloalkylene,
      • c at each occurrence is independently an integer from 1 to 10 and
      • R²⁷ at each occurrence is independently H, C_1-20-alkyl, or —Z²⁰—C_6-14-aryl,
        • wherein
        • Z²⁹ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • R²⁵ at each occurrence is independently C_1-30-alkyl, C_2-30-alkenyl or C_1-30-haloalkyl,
    • X⁸ at each occurrence is independently —Z²¹—O—Z²²—, —Z²¹—S—Z²²—, —S(O)—, —NR²⁸—, —C(O)O—, —(CO)NR²⁸, —C(O)S—, —O(CO)—, —S(CO)—, —NR²⁸C(O)—, —NR²⁸—, —Z²¹—SiR²⁸₂—Z²²—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
      • wherein
      • Z²¹ and Z²² at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
      • R²⁸ at each occurrence is independently H, C_1-20-alkyl, or —Z²³—C_6-14-aryl,
        • wherein
        • Z²³ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹² at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic hetrocyclic residue, each optionally substituted with 1 to 5 substituents R^o, wherein each R^o is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹⁴ and Ar¹⁵ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^p, wherein each R^p is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R²⁶ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl, C_1-20-alkoxy, —X⁹—Ar¹⁶, —X⁹—Ar¹⁷—Ar¹⁶, —X⁹—Ar¹⁷—R²⁹, or —X⁹—Ar¹⁷—Ar¹⁸—R²⁹,
      • wherein
      • X⁹ at each occurrence is independently —Z²⁴—O—Z²⁵—, —Z²⁴—S—Z²⁵, —S(O)—, —C(O)—, —C(O)O—, —(CO)NR³⁰, —C(O)S—, —O(CO)—, —S(CO)—, —NR³⁰C(O)—, —NR³⁰—, —Z²⁴—SiR³⁰₂—Z²⁵—, C_1-30-alkylene, C_2-30-alkenylene, C_1-30-haloalkylene or a covalent bond,
        • wherein
        • Z²⁴ and Z²⁵ at each occurrence are independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond, and
        • R³⁰ at each occurrence is independently H, C_1-20-alkyl or —Z²⁶—C_6-14-aryl,
        •  wherein
        •  Z²⁶ at each occurrence is independently C_1-6-alkylene, C_2-6-alkenylene, C_1-6-haloalkylene or a covalent bond,
    • Ar¹⁶ at each occurrence is independently C_6-14-aryl or monovalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 5 substituents R^q, wherein each R^q is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl,
    • Ar¹⁷ and Ar¹⁸ at each occurrence are independently C_6-14-arylene or bivalent 5 to 14 membered aromatic heterocyclic residue, each optionally substituted with 1 to 4 substituents R^r, wherein each R^r is independently selected from the group consisting of halogen, CN, C_1-6-alkyl, C_1-6-alkoxy and C_1-6-haloalkyl, and
    • R²⁹ at each occurrence is independently C_1-20-alkyl, C_2-20-alkenyl, C_1-20-haloalkyl or C_1-20-alkoxy,
• q and s are the same or different and are 0, 1, 2, 3, 4 or 5,
• r is 0, 1 or 2,and
• n is an integer from 1 to 10'000,
• which process comprises,
• preferably, (i) the step of reacting a compound of formula

• wherein A¹, A² and E are as defined above, and Hal is halogen, preferably —Br,
• with a compound of formula

• wherein G¹, G², L, q, r, and s are as defined above, and R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are the same and are C_1-30-alkyl, preferably C_1-6-alkyl, most preferably n-butyl or methyl,
• in the presence of a metal catalyst,or
• (ii) the step of reacting a compound of formula

• wherein A¹, A² and E, G¹, G², r and s are as defined above, and Hal is halogen, preferably —Br,
• with a compound of formula

• wherein L and r are as defined above, and R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are the same and are C_1-30-alkyl, preferably C_1-6-alkyl, most preferably n-butyl or methyl,in the presence of a metal catalyst,or
• (iii) the step of reacting a compound of formula

• wherein A¹, A² and E are as defined above, and R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are the same and are C_1-30-alkyl, preferably C_1-6-alkyl, most preferably n-butyl or methyl,
• with a compound of formula

• wherein G¹, G², L, q, r, and s are as defined above, and Hal is halogen, preferably —Br,
• in the presence of a metal catalyst,or
• (iv) the step of reacting a compound of formula

• wherein A¹, A², E, G¹, G², r and s are as defined above, and R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are the same and are C_1-30-alkyl, preferably C_1-6-alkyl, most preferably n-butyl or methyl,
• with a compound of formula

• wherein L and r are as defined above, and Hal is halogen, preferably —Br,
• in the presence of a metal catalyst.

Preferably R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are methyl or n-butyl.

The metal catalyst is preferably a palladium catalyst such tris(dibenzylideneacetone)dipalladium(0), preferably in combination with a phosphine such as tri-o-tolylphosphine. The reaction is preferably performed at elevated temperatures such 80 to 200° C., preferably 90 to 150° C. The reaction can be performed in an inert organic solvent such as chlorobenzene. The reaction can be stopped by the addition of end cappers such as 2-bromothiophene and 2-tributylstannylthiophene. The crude product may be worked up by conventional methods, for example by extracting the crude product with an appropriate solvent, for example with acetone.

Alternatively, the compound, oligomer or polymer of formula

• wherein A¹, A², E, G¹, L, G², q, r, s and n are as defined above,
• can be prepared by the process as outlined above but using

• wherein G¹, G², L, q, r, and s are as defined above, and R³⁷, R³⁸, R³⁹ and R⁴⁰ are the same and are H or C_1-30-alkyl, or R³⁷ and R³⁸, respectively, R³⁹ and R⁴⁰ form together with —O—B—O— a 5 to 8-membered cyclic ring, for example a pinacol type ring of formula

• instead of the compound of formula 3,

• wherein L and r are as defined above, and R³⁷, R³⁸, R³⁹ and R⁴⁰ are the same and are H or C_1-30-alkyl, or R³⁷ and R³⁸, respectively, R³⁹ and R⁴⁰ form together with —O—B—O— a 5 to 8-membered cyclic ring, for example a pinacol type ring of formula

• instead of the compound of formula 9,

• wherein A¹, A² and E are as defined above, and R³⁷, R³⁸, R³⁹ and R⁴⁰ are the same and are H or C_1-30-alkyl, or R³⁷ and R³⁸, respectively, R³⁹ and R⁴⁰ form together with —O—B—O— a 5 to 8-membered cyclic ring, for example a pinacol type ring of formula

• instead of the compound of formula 10, or

• wherein A¹, A², E, G¹, G², r and s are as defined above, and R³⁷, R³⁸, R³⁹ and R⁴⁰ are the same and are H or C_1-30-alkyl, or R³⁷ and R³⁸, respectively, R³⁹ and R⁴⁰ form together with —O—B—O— a 5 to 8-membered cyclic ring, for example a pinacol type ring of formula

• instead of the compound of formula 12.

The compound of formula

• wherein A¹ and A² are as defined above, and Hal is halogen, preferably —Br, and E is

• wherein R¹, R² and R³ are as defined above,
• can be prepared by a process, which comprises the step of reacting a compound of formula

• wherein A¹, A² and E are as defined above, and R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl,
• with a halogenating agent in the presence of an acidic catalyst.

The halogenating agent is preferably —Br₂. The acidic catalyst is preferably trichloroacetic acid. The reaction is preferably carried out in an inert organic solvent such as chloroform. The reaction is preferably carried out at ambient temperature, for example at a temperature from 15 to 30° C., more preferably at a temperature from 18 to 26° C. The reaction mixture can be worked up by conventional methods.

The compound of formula

• wherein A¹, A² and E are as defined above, and R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl,
• can be prepared by a process, which comprises the step of coupling a compound of formula

• wherein A¹, A², R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are as defined above, and Hal is halogen, preferably —Br,
• with H-E-H or

• wherein R⁴⁷, R⁴⁸, R⁴⁹ and R⁵⁰ are the same and are H or C_1-30-alkyl, or R⁴⁷ and R⁴⁸, respectively, R⁴⁹ and R⁵⁰ form together with —O—B—O— a 5 to 8-membered cyclic ring, for example a pinacol type ring of formula.

• in the presence of a metal catalyst.

The metal catalyst can be a palladium catalyst such as tetrakis(triphenylphosphine)palladium(0), or tris(dibenzylideneacetone)dipalladium(0) in combination with a phosphine such as rac-BINAP or tri-tert-butylphosphine. Preferably, the reaction is carried out in the presence of a base such as potassium carbonate or sodium tert-butoxide. The reaction can be carried out in an inert organic solvent such as toluene, or in mixtures of inert organic solvents and water, for example in mixtures of toluene and water. The reaction can be carried out at elevated temperatures, for example at a temperature from 70 to 200° C., preferably at a temperature from 80 to 150° C. The reaction mixture can be worked up by conventional methods.

If E is

• the vic-bis(pinacolatoboryl) complex

• is preferably used in the reaction.

This vic-bis(pinacolatoboryl) complex can be synthesized via platinum catalyzed boronation of

The compound of formula

• wherein A¹ and A² are as defined above, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably, C_1-20-alkyl, preferably C_1-6-alkyl, more preferably isopropyl, and Hal is halogen, preferably —Br,
• can be prepared by a process which comprises the step of reacting

• wherein A¹ and A² are as defined above, and Hal is halogen, preferably —Br, with R⁴¹R⁴²R⁴³Si-Hal and R⁴⁴R⁴⁵R⁴⁶Si-Hal and a base, wherein R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are as defined above, and Hal is halogen, preferably —Br.

An example of a base is lithium diisopropylamide. The reaction can be performed in an inert organic solvent, for example THF. The reaction can be performed at a temperature of 0 to −100° C., preferably at −40 to −90° C., preferably at around −78° C. The reaction mixture obtained can be worked-up by conventional methods.

The compound of formula

• wherein A¹ and A² are as defined above, and Hal is halogen, preferably —Br,
• can be prepared by a process comprising the step of reacting

• wherein A¹ and A² are as defined above,
• with a halogenating agent.

An example of a halogenating agent is N-bromosuccinimide. The reaction can be performed in an inert organic solvent, for example DMF. The reaction can be performed at elevated temperature, for example at a temperature from 20 to 100° C., preferably at 40 to 80° C. The reaction mixture obtained can be worked-up by conventional methods.

A compound of formula 2d can also be prepared via thiocyanation of 2,6-diamino-benzothiazole 18 as reported by Landquist, J. K. J. Chem. Soc. C 1967, 2212 to 2220, followed by Sandmeyer reaction as depicted below

A compound of formula 2e can also be prepared via condensation of 3,6-diamino-1,2-phenylene dihydrogen thiosulphate 19 with thiophene-2-carboxylic acid in analogy to the processes described by Green, A. G. J. Chem. Soc., Trans. 1903, 83, 1201 to 1212, and by Cox, R. J.; Clecak, N. J. J. Org. Chem. 1968, 33, 2132 to 2133, followed by halogenation as depicted below

The compound of formula

• wherein A¹ and A² are as defined above, and Hal is halogen, preferably —Br, and E is selected from the group consisting of

• wherein R⁴, R⁵, R¹⁹, R²⁰ and R²¹ are as defined above,
• can be prepared by a process, which comprises the step of reacting a compound of formula

• wherein A¹ and A² are as defined above, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl, and Hal is halogen, preferably —Br,
• with a suitable compound to incorporate E,
• in the presence of a base such as butyl lithium.

For example, the compounds of formulae 2f, 2g, 2h and 2i can be prepared as follows:

The compound of formula

• wherein A¹ and A² are as defined above, and Hal is halogen, preferably —Br, and E is selected from the group consisting of

• wherein R⁴, R⁵, R¹⁹, R²⁰ and R²¹ are as defined above,
• can also be prepared by a process, which comprises the step of reacting a compound of formula

• wherein A¹ and A² are as defined above, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl,
• with a suitable compound to incorporate E,
• in the presence of a base such as lithium diisopropylamide, for example as described for similar compounds in WO 2009/069687.

The compound of formula

• wherein A¹ and A² are as defined above, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl,
• can be prepared via oxidative coupling of

For example the compound of formula 20a can be prepared as follows:

The compound of formula

• wherein
• A¹ and A² can be the same or different and are S or Se,
• E is selected from the group consisting of

• wherein
• R¹, R², R³, R⁴, R⁵, R¹⁹, R²⁰ and R²¹ are as defined above,

G¹ and G² are as defined above,

• q and s are as defined above, and
• Hal is halogen,
• can be prepared by reacting the compound of formula

• wherein A¹ and A² are as defined above, and Hal is halogen,
• with suitable compounds to incorporate G¹ and G², such as stannyl functionalized G¹ and G² or borate functionalized G¹ or G² or Grignard functionalized G¹ and G², in the presence of a metal catalyst,
• followed by halogenation.

For example, the compound of formula 8a can be prepared as follows:

Also part of the invention is the compound of formula

• wherein
• A¹ and A² can be the same or different and are S or Se,
• E is selected from the group consisting of

• wherein
• R¹, R², R³, R⁴, R⁵, R¹⁹, R²⁰ and R²¹ are as defined above and Hal is halogen.

Also part of the invention is the compound of formula

• wherein
• A¹ and A² can be the same or different and are S or Se,
• E is

and R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl.

Also part of the invention is a compound of formula

• wherein A¹ and A² can be the same or different and are S or Se,
• R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are C_1-30-alkyl, preferably C_1-6-alkyl, more preferably isopropyl, and Hal is halogen, preferably —Br.

Also part of the present invention is an electronic device comprising the compounds, oligomers and polymers of the present invention.

The electronic device can be any electronic device, for example an organic photovoltaic (OPV) cell, an organic field-effect transistor (OFET) or an organic light emitting diode (OLED). Preferably, it is an organic field-effect transistor.

The organic field effect transistor comprising the compounds, oligomers and polymers of the present invention can be prepared by solution deposition of a solution of the compounds, oligomers and polymers of the present invention in a suitable solvent. The solvent can be an organic solvent, for example 1,2-dichlorobenzene. Solution deposition can be performed by methods known in the art, for example by spin coating, for example at 2000 rpm, 255 acc (acc: spin acceleration), 1 minute.

The organic field effect transistor can have any architecture known in the art, for example a bottom gate bottom contact (BGBC) architecture as depicted in FIG. 1. When the organic field effect transistor has a bottom gate bottom contact (BGBC) architecture, the substrate (or gate electrode), the gate dielectric, and the source and drain electrodes can be any substrate, gate dielectric, source and drain electrode known in the art. For example, the substrate (or gate electrode) can be heavily doped silicon wafer, the gate dielectric can be thermally grown silica, and the source and drain electrode can be made of gold which is lithographically patterned. Before deposition of the compounds, oligomers and polymers of the present invention as semiconductors, the device can be vapor treated with hexamethyldisilazane (HMDS).

Also part of the invention is the use of the compound, oligomer or polymer of the present invention as organic semiconducting material.

The compounds, oligomers and polymers of the present invention show a surprising high ionization potential, which may contribute to better ambient oxidative stability. The compounds, oligomers and polymers of the present invention are compatible with liquid processing techniques and are suitable for use as semiconductors in organic field effect transistors. The organic field effect transistor using the compounds, oligomers and polymers of the present invention as semiconductors show good field-effect mobilities and on/off ratios.

FIG. 1 shows an organic field effect transistor having a bottom gate bottom contact (BGBC) architecture.

EXAMPLES

Example 1

Preparation of 2,2′-dibromo-(5,6-dihexylbenzo[2,1-d;3,4-d′]bisthiazole) (2a)

Preparation of 4,4′-dibromo-5,5′-bithiazole (6a)

N-bromosuccinimide (6.35 g, 35.66 mmol, 4 eq.) is added to a stirred homogeneous solution of 5,5′-bithiazole (7a) (1.5 g, 8.9 mmol) in anhydrous DMF (125 mL). The reaction mixture is heated at 60° C. for 3 hours. The reaction mixture is washed subsequently with an aqueous solution of 10% sodium bicarbonate (200 mL), extracted with dichloromethane (200 mL), washed with water (3×100 mL) and sodium chloride saturated water (100 mL), and dried over anhydrous sodium sulfate. The crude product is re-crystallized from dichloromethane/n-hexane (1:10). Yellowish crystals are obtained. ¹H-NMR (d-chloroform) (400 MHz): δ 8.87 (s, 2H). ¹³C-NMR (d-chloroform) (400 MHz): δ 154.8, 129.3, 122.5.

Preparation of 2,2′-bis(triisopropylsilyl)-4,4′-dibromo-5,5′-bithiazole (5a)

1.84 mL of a 2M solution of lithium diisopropylamide (0.39 g, 3.68 mmol, 2.4 eq.) in THF is added dropwise to a solution of 4,4′-dibromo-5,5′-bithiazoles (6a) (0.5 g, 1.53 mmol) in anhydrous THF (20 mL) at −78° C. over 10 minutes. The reaction mixture is allowed to stir for 3 hours, and then triisopropylsilyl chloride (0.709 g, 0.79 mL, 3.68 mmol, 2.4 eq.) is added slowly. The reaction mixture is warmed up to room temperature overnight. The reaction mixture is diluted with ethyl acetate (140 mL), and the organic layer is washed with sodium bicarbonate saturated water (70 mL) and sodium chloride saturated water (70 mL), dried over magnesium sulfate and concentrated in vacuo. Column chromatography using gradient solvent from n-hexane to ethyl acetate/n-hexane (5/95) provides a yellow solid. ¹H-NMR (d-chloroform) (400 MHz): δ 2.43-1.5 (m, J=8 Hz, 6H), δ 1.16-1.18 (d, J=7.6 Hz, 36H). ¹³C-NMR (d-chloroform) (400 MHz): δ 172.7, 130.5, 125.1, 18.7, 11.8.

Preparation of 2,2′-bis(triisopropylsilyl)-(5,6-dihexylbenzo[2,1-d;3,4-d′]bisthiazole) (4a)

A mixture of 5a (0.5 g, 0.783 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.090 g, 0.078 mmol, 0.1 eq.) is degassed 3 times. A solution of vic-bis(pinacolatoboryl)-7-tetradecene (0.456 g, 1.018 mmol, 1.3 eq.), in anhydrous toluene (5 mL) is added, followed by 12 mL of toluene (total 17 mL anhydrous toluene). Subsequently 2.8 mL of degassed aqueous solution of potassium carbonate (0.64 g, 4.70 mmol, 6 eq.) is added. The reaction mixture is stirred and heated at 100° C. overnight. The reaction mixture is allowed to cool to room temperature, and is diluted with ethyl acetate (50 mL). The resulting reaction mixture is washed with ammonium chloride saturated water (50 mL) and the aqueous layer is extracted with ethyl acetate (3×50 mL). The combined organic layers are washed with sodium chloride saturated water (25 mL), dried over magnesium sulfate, and concentrated in vacuo. Column chromatography using a gradient solvent from n-hexane to ethyl acetate/n-hexane (10/90) provides an off-white solid. ¹H-NMR (d-chloroform) (400 MHz): δ 3.37 (dd, J=8 Hz, 4H), δ 1.74-1.76 (m, J=8 Hz, 4H), δ 1.47-1.55 (m, J=8 Hz, 6H), δ 1.33-1.37 (m, J=8 Hz, 12H), δ 1.2-1.22 (d, J=8 Hz, 36H), δ 0.87-0.92 (t, J=7.6 Hz, 6H). LC-MS: 95% purity with m/z 673.4.

Preparation of 2,2′-dibromo-(5,6-dihexylbenzo[2,1-d;3,4-d′]bisthiazole) (2a)

A solution of bromine (0.34 g, 0.11 mL, 2.11 mmol, 4 eq.) in chloroform (5 mL) containing trichloroacetic acid (7 mg) is added dropwise and slowly to a solution of 4a (0.355 g, 0.527 mmol) in chloroform (8 mL) at 0° C. The reaction mixture is stirred at room temperature for 3 days. The reaction mixture is diluted with dichloromethane (50 mL), washed with an aqueous solution of 20 weight % sodium thiosulfate (50 mL) and with an aqueous solution of 10 weight % sodium bicarbonate (50 mL). Subsequently the organic layer is dried over magnesium sulfate and concentrated in vacuo. Purification by column chromatography (ethyl acetate/n-hexane (10/90)) followed by re-crystallisation from ethanol affords light brown crystals. ¹H-NMR (d-chloroform) (400 MHz): δ 3.17 (dd, J=8 Hz, 4H), δ 1.66 (m, J=8 Hz, 4H), δ 1.47 (m, J=8 Hz, 4H), δ 1.35 (m, J=8 Hz, 8H), δ 0.92 (t, J=7.6 Hz, 6H). LC-MS: 98% purity with m/z 519. Elemental analysis (calcd): C, 46.34 (46.36); H, 5.06 (5.09).

Example 2

Preparation of poly(benzobisthiazole-cyclopentadithiophene) (1a)

Dibromo-benzobisthiazole (2a) (60 mg, 0.116 mmol, 1 eq.), bis(trimethylstannyl)cyclopentadithiophene (3a) (110 mg, 0.116 mmol, 1 eq.), tris(dibenzylidene-acetone)dipalladium(0) (3.2 mg, 0.003 mmol, 3% eq.) and tri-o-tolylphosphine (2.1 mg, 0.007 mmol, 6% eq.) are added into a Schlenk flask and degassed 3 times. Chlorobenzene (4 mL) is added and the reaction mixture is stirred at 100° C. overnight then at 130° C. for 2 days. 2-Bromothiophene (0.01 mL) and 2-tributylstannylthiophene (0.01 mL) are added as end cappers, with 2-bromothiophene added first followed by 2-tributylstannylthiophene 2 hours later. After another 2 hours stirring, the reaction mixture is cooled to room temperature. The reaction mixture is then added dropwise to methanol (200 mL), filtered, and then subjected to Soxhlet extraction with acetone. The polymer is recovered as solid mass and showed Mn=8360 g/mol (Mw=24264 g/mol & PDI=2.92). Elemental analysis (calcd): C, 70.77 (74.48); H, 8.93 (9.63).

Example 3

Preparation of poly(benzobisthiazole-bisthienylethylene) (1b)

Dibromo-benzobisthiazole (2a) (55 mg, 0.106 mmol, 1 eq.) prepared as described in example 1, bis(2-trimethylstannyl-4-dodecylthienyl)ethylene (3b) (90.7 mg, 0.106 mmol, 1 eq.), tris(dibenzylideneacetone)dipalladium(0) (2.9 mg, 0.003 mmol, 3% eq.) and tri-o-tolylphosphine (1.9 mg, 0.006 mmol, 6% eq.) are added into a Schlenk flask and degassed 3 times. Chlorobenzene (2 mL) is added and the reaction mixture is stirred at 130° C. for 2 days. 2-Bromothiophene (0.01 mL) and 2-tributylstannylthiophene (0.01 mL) are added as end cappers, with 2-bromothiophene added first followed by 2-tributylstannylthiophene 2 hours later. After another 2 hours stirring, the reaction mixture is cooled to room temperature. The mixture is filtered and the filtrate is concentrated and added dropwise to methanol (200 mL), filtered, and then subjected to Soxhlet extraction with acetone. The polymer is recovered as solid mass and showed Mn=3368 g/mol (Mw=4749 g/mol & D=1.41).

Example 4

Preparation of poly(benzobisthiazole-bithiophene) (1c)

Preparation of 2,2′-dibromo-(5,6-dimethylbenzo[2,1-d;3,4-d′]bisthiazole) (2b)

Dibromo-benzobisthiazole (2b) is prepared in analogy to 2,2′-dibromo-(5,6-dihexylbenzo[2,1-d;3,4-d′]bisthiazole) (2a) in example 1, except that vic-bis(pinacolatoboryl)-2-butene (with the equivalent of 1.3 eq to the substrate 5a) is used instead of vic-bis(pinacolatoboryl)-7-tetradecene (with the equivalent of 1.3 eq to the substrate 5a).

Preparation of poly(benzobisthiazole-bithiophene) (1c)

Dibromo-benzobisthiazole (2b) (79 mg, 0.209 mmol, 1 eq.) is added as a 4.2 mL chlorobenzene solution into a pre-degassed mixture of bis(2-trimethylstannyl-2-dodecylthiophene) (3c) (173.1 mg, 0.209 mmol, 1 eq.), tris(dibenzylideneacetone)dipalladium(0) (5.7 mg, 0.003 mmol, 3% eq.) and tri-o-tolylphosphine (3.8 mg, 0.006 mmol, 6% eq.). The reaction mixture is stirred at 130° C. for 2 days. After two days of reaction, tris(dibenzylideneacetone)-dipalladium(0) (5.7 mg, 0.003 mmol, 3% eq.) and tri-o-tolylphosphine (3.8 mg, 0.006 mmol, 6% eq.) is added. After four days of reaction, another portion of tris(dibenzylidene-acetone)dipalladium(0) (5.7 mg, 0.003 mmol, 3% eq.) and tri-o-tolylphosphine (3.8 mg, 0.006 mmol, 6% eq.) is added. After total 6 days, the polymerization is stopped by the addition of 2-bromothiophene (0.01 mL) and 2-tributylstannylthiophene (0.01 mL). 2-Bromothiophene is added first followed by 2-tributylstannylthiophene 4 hours later. After another 24 hours stirring, the reaction mixture is cooled to room temperature. The mixture is filtered and the filtrate is concentrated and added dropwise to a methanolic solution of 5 weight % HCl (200 mL). The polymer is filtered and before soxhlet extraction in acetone showed Mn=959 g/mol (Mw=1410 g/mol & D=1.47).

Example 5

Preparation of N-4-decylaniline-2,6-dibromo dithiazolo[2,3-d;3′,2′-b]pyrrole (2c)

Preparation of N-4-decylaniline-2,6-bis(triisoproylsilyl)dithiazolo[2,3-d;3′,2′-b]pyrrole) (4b)

A mixture of bis(triisopropylsilyl)-dibromobithiazole (5a) (790 mg, 1.237 mmol), tris(dibenzylideneacetone)dipalladium(0) (113 mg, 0.123 mmol, 0.1 eq.), sodium tert-butoxide (200 mg, 2.968 mmol, 2.4 eq.) and rac-BINAP (153 mg, 0.347 mmol, 0.2 eq.) is degassed 3 times. 4-n-Decylaniline (360 mg, 1.546 mmol, 1.25 eq.) in anhydrous toluene (18 mL) is added. The reaction mixture is stirred and heated at 100° C. for 2 days under nitrogen. After the mono-aminated intermediate is formed tris(dibenzylidene-acetone)dipalladium(0) (56 mg, 0.061 mmol, 0.05 eq.) and 0.36 mL of a 10 weight % solution of tri-tert-butylphosphine (24 mg, 0.173 mmol, 0.1 eq.) in n-hexane is added. The reaction mixture is stirred at 100° C. for 2 days under nitrogen. Afterwards the reaction mixture is diluted with ethyl acetate (100 mL). The resulting reaction mixture is washed with ammonium chloride saturated water (100 mL) and the aqueous layer is extracted with ethyl acetate (3×70 mL). The combined organic layers are washed with sodium chloride saturated water (50 mL), dried over magnesium sulfate, and concentrated in vacuo. Column chromatography using ethyl acetate/n-hexane (2/98) provided off-white solid. ¹H-NMR (d-chloroform) (400 MHz): δ 8.58 (d, J=9.6 Hz, 2H), δ 7.34 (d, J=8.4 Hz, 2H), δ 2.28 (dd, J=8 Hz, 2H), δ 1.65 (m, J=8 Hz, 2H), δ 1.52-1.46 (m, J=8 Hz, 6H), δ 1.27 (s, 14H), δ 1.19-1.21 (d, J=8 Hz, 36H), δ 0.88 (t, J=7.6 Hz, 3H).

Preparation of N-4-decylaniline-2,6-dibromo dithiazolo[2,3-d;3′,2′-b]pyrrole (2c)

A solution of bromine (0.16 g, 0.05 mL, 1.01 mmol, 4 eq.) in chloroform (3 mL) containing trichloroacetic acid (4 mg) is slowly and dropwise added to a solution of 4b (0.180 g, 0.253 mmol) in chloroform (4 mL) at 0° C. The reaction mixture is stirred at room temperature for 2 days. The reaction mixture is diluted with dichloromethane (50 mL), washed with an aqueous solution of 20 weight % sodium thiosulfate (50 mL) and an aqueous solution of 10 weight % sodium bicarbonate (50 mL). Subsequently the organic layer is dried over magnesium sulfate and concentrated in vacuo. Purification by column chromatography using n-hexane followed by re-crystallisation from n-hexane affords white flakes. ¹H-NMR (d-chloroform) (400 MHz): δ 7.88 (d, J=8.4 Hz, 2H), δ 7.35 (d, J=8 Hz, 2H), δ 2.66 (dd, J=7.6 Hz, 2H), δ 1.63 (m, J=7.6 Hz, 2H), δ 1.28 (s, 14H), δ 0.88 (t, J=7.6 Hz, 3H). LC-MS: 97.2% purity with m/z 556. Elemental analysis (calcd): C, 47.54 (47.58); H, 4.46 (4.54).

Example 6

Preparation of poly(dithiazolopyrrole-bisthienylethylene) (1d)

Dibromo-dithiazolopyrrole (2c) (36 mg, 0.065 mmol, 1 eq.) prepared as described in example 5, bis(2-trimethylstannyl-4-dodecylthienyl)ethylene (3d) (55.4 mg, 0.065 mmol, 1 eq.), tris(dibenzylideneacetone)dipalladium(0) (3.6 mg, 0.004 mmol, 6% eq.) and tri-o-tolylphosphine (2.4 mg, 0.008 mmol, 12% eq.) are added into a Schlenk flask and degassed 3 times. Chlorobenzene (1.5 mL) is added and the reaction mixture is stirred at 130° C. for 2 days. After two days of reaction, tris(dibenzylideneacetone)dipalladium(0) (3.6 mg, 0.004 mmol, 6% eq.) and tri-o-tolylphosphine (2.4 mg, 0.008 mmol, 12% eq.) was added. After total reaction of 3 days, the polymerization is stopped by the addition of 2-bromothiophene (0.01 mL) followed by 2-tributylstannylthiophene (0.01 mL) 3 hours later. After another 3 hours stirring, the reaction mixture is cooled to room temperature and added dropwise to methanol (100 mL), filtered, and then subjected to Soxhlet extraction with acetone. The polymer is recovered as solid mass and showed Mn=4305 g/mol (Mw=7571 g/mol & D=1.76).

Measurement of the Ionization Potential of Polymer 1a

The oxidative stability of π-conjugated polymers may be contributed by their ionization potential (IP), that is, on the energy of the highest occupied molecular orbital (HOMO) with respect to vacuum. The ionization potential (IP) is also reflected as negative value of the HOMO energy level (E_HOMO) of a molecule, oligomer or polymer,IP=−E_HOMO and can be measured by cyclic voltammetry (CV).

The HOMO energy levels (E_HOMO) of poly(benzobisthiazole-cyclopentadithiophene) (1a), prepared as described in example 2, and comparative polymer 22a, which is described by Xiao, S; Zhou H.; You, W. in Macromolecules 2008, 41, 5688-5696, are determined by cyclic voltammetry (CV).

Cyclic voltamogramms are recorded from thin films of polymer 1a, respectively comparative polymer 22a, drop-casted from 0.5 mg/mL chloroform solutions. A Pt disk is used as a working electrode and Ag/AgCl reference electrode is employed. The measurement is done in tetrabutylammonium tetrafluoroborate as electrolyte and ferrocene/ferrocenium redox couple (Fc/Fc⁺) is used as an internal reference, which has a known reduction potential of 4.8 eV. The electrochemical (oxidation and reduction) onset is determined at the position where the current starts to differ from the baseline and the HOMO energy level (E_HOMO) is calculated from the onset oxidation potential (E_Ox), as shown in the equation below:E_HOMO=−(E_Ox+4.8)[eV]

The results are outlined in table 1.

TABLE 1
polymer           EHOMO [eV]
1a                −5.44
22a (comparative) −5.04

As can be derived from table 1, the HOMO energy level (E_HOMO) value of polymer 1a is decreased by 0.4 eV compared to the HOMO energy level (E_HOMO) value of comparative polymer 22a, and thus the ionization potential (IP) and consequently the oxidative stability of polymer 1a is higher than the one of comparative polymer 22a.

Fabrication of an Organic Field-Effect Transistor Using Polymer 1a as Semiconductor

An organic field effect transistor is made in bottom gate bottom contact (BGBC) architecture, as depicted in FIG. 1. Heavily doped Si wafer are used as substrate and gate electrode with 200 nm thermally grown SiO₂ serving as gate dielectric. Source and drain electrode are made of gold which is lithographically patterned. Before semiconductor deposition, the substrate is vapor treated with hexamethyldisilazane (HMDS). The polymer 1a solution is prepared by solubilizing the polymer 1a in 1,2-dichlorobenzene and heating it inside oven until soluble. Subsequently, semiconductor solution deposition of the polymer 1a is done by spin coating (deposition condition: 2000 rpm, 255 acc, 1 minute). The organic field effect transistor is made in ambient environment.

Testing of the Organic Field-Effect Transistor Using Polymer 1a as Semiconductor

The hole mobility (μ_p), onset voltage (V_on, voltage when the drain current increases abruptly and can be measured), and the on/off ratio of the organic field effect transistor using polymer 1a as semiconductor are determined at room temperature and after annealing at 200° C. for 30 minutes, in order to observe the effect of annealing on the semiconductor performance. The organic field effect transistor is tested in ambient environment. Channel length (L)=5 μm, Channel width (W)=350 μm, W/L=70. Measurement is performed at: gate voltage (Vg)=sweep from 20 to −90 V, drain voltage (Vd)=−90 V,

The results are outlined in table 2.

TABLE 2
	hole mobility
	μp [cm2/Vs]	Von [V]	On/Off ratio
at RT	0.2 × 10−3	−5	2.66 × 104
after annealing at 200° C.	1.06 × 10−3	5	6.01 × 104

Claims

1. An oligomer or polymer of formula

2. The oligomer or polymer of formula (1) of claim 1 wherein E is

3. An oligomer or polymer of formula (1)

4. The oligomer or polymer of formula (1) of claim 1, wherein R3 is —X5—Ar8—R13, whereinX5 is a covalent bond,Ar8 is C6-14-arylene, andR13 is C1-20-alkyl.

5. The oligomer or polymer of formula (1) of claim 1, wherein G1 and G2 are the same or different and are phenylene,

6. The oligomer or polymer of formula (1) of claim 1, wherein G1 and G2 are the same or different and are a monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue which monocyclic bivalent 5 to 8 membered aromatic heterocyclic residue is

7. The oligomer or polymer of formula (1) of claim 1, wherein each Ri is independently C1-30-alkyl.

8. The oligomer or polymer of formula (1) of claim 1, wherein L is a bivalent 5 to 18 membered aromatic heterocyclic residue, wherein the bivalent 5 to 18 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rl, wherein each Rl is independently selected from the group consisting of C1-30-alkyl, —Z18—O—C1-30-alkyl, —Z18—S—C1-30-alkyl, —Z18—C3-10-cycloalkyl, —Z18—C6-14-aryl, —Z18-monovalent 3 to 12 membered aliphatic heterocyclic residue and —Z18-monovalent 5 to 14 membered aromatic heterocyclic residue,wherein C1-30-alkyl, C3-10-cycloalkyl, C6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rm, wherein each Rm is independently selected from the group consisting of halogen, —CN and *═O, andwherein C3-10-cycloalkyl, C6-14-aryl, monovalent 3 to 12 membered aliphatic heterocyclic residue and monovalent 5 to 14 membered aromatic heterocyclic residue is optionally substituted with 1 to 4 substituents Rn, wherein each Rn is independently selected from the group consisting of C1-20-alkyl, C1-20-alkoxy, C1-20-haloalkyl,whereinZ18 at each occurrence is independently C1-6-alkylene, C1-6-haloalkylene or a covalent bond,orL is

9. The oligomer or polymer of formula (1) of claim 1, wherein L is a bivalent 5 to 18 membered aromatic heterocyclic residue selected from the group consisting of

10. The oligomer or polymer of formula (1) of claim 1, wherein L is

11. The oligomer or polymer of formula (1) of claim 1, wherein q, r and s are 0 or 1, with the proviso that q, r and s are not all 0 at the same time.

12. The oligomer or polymer of formula (1) of claim 1, wherein n is an integer from 2 to 5000.

13. An electronic device comprising the oligomer or polymer of formula (1) of claim 1.

14. The electronic device of claim 13, wherein the electronic device is an organic field effect transistor.

15. The oligomer or polymer of formula (1) of claim 4, wherein Ar8 is phenylene.

16. The oligomer or polymer of formula (1) of claim 1, wherein n is an integer from 2 to 1000.

17. The oligomer or polymer of formula (1) of claim 1, wherein n is an integer from 2 to 100.

18. The oligomer or polymer of formula (1) of claim 1, wherein n is an integer from 2 to 30.

19. The oligomer or polymer of formula (1) of claim 1, wherein R3 is H, halogen, —CN, C2-30-alkenyl, C2-20-alkynyl, C3-10-cycloalkyl, C5-10-cycloalkenyl, C8-10-cycloalkynyl, C1-30-haloalkyl, monovalent 3 to 12 membered aliphatic heterocyclic residue, —X4—R12, —X5—Ar7, —X5—Ar8—Ar7, —X5—Ar8—R13 or —X5—Ar8—Ar9—R13.

20. The oligomer or polymer of formula (1) of claim 1, wherein each Ri is independently n-octyl, n-(2-ethyl)hexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C20).

21. The oligomer or polymer of formula (1) of claim 1, wherein each Ri is n-dodecyl.