Patent Application
20080125609
The present invention relates to new types of compounds and to their use in organic electroluminescent devices.
The use of semiconductive organic compounds in organic electroluminescent devices (OLEDs) is just starting to be introduced onto the market. The general structure of such devices is described, for example, in U.S. Pat. No. 4,539,507, U.S. Pat. No. 5,151,629, EP 0676461 and WO 98/27136. Devices comprising simple OLEDs have already been introduced onto the market as demonstrated by the car radios from Pioneer, is the mobile telephones from Pioneer and SNMD or a digital camera from Kodak with an organic display. Further products of this type will shortly be introduced. However, these devices still exhibit considerable problems which are in need of urgent improvement:
The closest prior art may be specified as the use of particular arylvinylamines which do not have further substitution on the double bond of the stilbene-like system by Idemitsu (for example WO 04/013073, WO 04/016575, WO 04/018587). Using these, good lifetimes are reported for deep blue emissions. However, these results are greatly dependent upon the host material used, so that the cited lifetimes cannot be compared as absolute values, but rather always only in the case of use in an optimized host system. Moreover, these compounds are thermally unstable and cannot be evaporated without decomposition, which therefore entails a high level of technical complexity for the vapour deposition and thus a distinct technical disadvantage. A further disadvantage is the emission colour of these compounds. While Idemitsu reports deep blue emission (CIE y coordinates in the range of 0.15-0.18), it has not been possible to reproduce these colour coordinates in simple devices according to the prior art. On the contrary, green-blue emission with CIE y coordinates in the range of 0.30-0.35 is obtained here. It is not apparent how blue emission can be obtained with these compounds.
We suspect that the double bonds of the compounds described in the literature might be responsible at least for some of the abovementioned problems. For instance, the double bond might tend to polymerize in the course of heating (for example in the course of sublimation to purify the compounds or in the course of vapour deposition in the production of the device), or might isomerize from the trans to the cis configuration in the excited state in the course of operation of the device. Even in the event of identical substitution, in which case the consequence of isomerization is not so severe because the product has the same structure as the reactant, it deactivates the excitation energy of the molecule in a non-radiative manner. These side reactions might therefore reduce the efficiency or the lifetime of the organic electronic device. Moreover, these side reactions are possibly responsible for the low thermal stability of these compounds.
There is thus still a need for blue-emitting compounds which lead to good efficiencies and simultaneously to high lifetimes in organic electroluminescent devices, and which are thermally stable and can thus be processed in a technically unproblematic manner. It has now been found that, surprisingly, organic electroluminescent devices which comprise certain compounds, detailed below, whose double bonds cannot exhibit cis-trans-isomerization by virtue of the chemical structure as blue-emitting dopants in a host material have distinct improvements over the prior art. It is possible with these materials to simultaneously obtain high efficiencies and long lifetimes. In other functions, too, these materials in organic electroluminescent devices and further organic electronic devices exhibit good properties. Moreover, these compounds, unlike materials according to the prior art, can be sublimed and applied by vapour deposition without noticeable decomposition and are therefore distinctly easier to handle than materials according to the prior art. These compounds and their use in organic electronic devices therefore form part of the subject-matter of the present invention.
The invention provides compounds of the formula (1),
Even if it is evident from the description, it should be pointed out explicitly once again here that the R1 radicals can also form a ring system with one another and can thus in particular form a spiro system.
An aryl group in the context of this invention contains 6 to 40 carbon atoms; a heteroaryl group in the context of this invention contains 2 to 40 carbon atoms and at least 1 heteroatom, with the proviso that the sum of carbon atoms and heteroatoms adds up to at least 5. The heteroatoms are preferably selected from N, O and/or S. An aryl group or heteroaryl group refers either to a simple aromatic cycle, i.e. benzene, or a simple heteroaromatic cycle, for example, pyridine, pyrimidine, thiophene, etc., or a fused aryl or heteroaryl group.
An aromatic ring system in the context of this invention contains 6 to 40 carbon atoms in the ring system. A heteroaromatic ring system in the context of this invention contains 2 to 40 carbon atoms and at least one heteroatom in the ring system, with the proviso that the sum of carbon atoms and heteroatoms adds up to at least 5. The heteroatoms are preferably selected from N, O and/or S. In the context of this invention, an aromatic or heteroaromatic ring system shall be understood to mean a system which does not necessarily contain only aryl or heteroaryl groups, but in which a plurality of aryl or heteroaryl groups may also be interrupted by a short non-aromatic unit (fewer than 10% of the atoms other than H, preferably fewer than 5% of the atoms other than H), for example an sp3-hybridized carbon, nitrogen or oxygen atom. For example, aromatic ring systems in the context of this invention should also be understood to mean systems such as 9,9′-spirobifluorene, 9,9-diarylfluorene, triarylamine, diaryl ether, etc. In this case, a portion of the aromatic or heteroaromatic ring system may also be a fused group.
In the context of the present invention, a C1- to C40-alkyl group in which individual hydrogen atoms or CH2 groups may also be substituted by the above-mentioned groups is more preferably understood to mean the methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 2-bethylbutyl, n-pentyl, s-pentyl, cyclopentyl, n-hexyl, cyclohexyl, n-heptyl, cycloheptyl, n-octyl, cyclooctyl, 2-ethylhexyl, trifluoromethyl, pentafluoroethyl, 2,2,2-trifluoroethyl, ethenyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl, ethynyl, propynyl, butynyl, pentynyl, hexynyl or octynyl radicals. A C1- to C40-alkoxy group is more preferably understood to mean methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy or 2-methylbutoxy. An aromatic or heteroaromatic ring system which has 5-40 aromatic ring atoms, and may also be substituted in each case by the abovementioned R radicals and which may be attached via any positions to the aromatic or heteroaromatic is understood in particular to mean groups which are derived from benzene, naphthalene, anthracene, phenanthrene, pyrene, chrysene, perylene, fluoranthene, naphthacene, pentacene, benzpyrene, biphenyl, biphenylene, terphenyl, terphenylene, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis- or trans-indenofluorene, truxene, isotruxene, spirotruxene, spiroisotruxene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6-quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline, phenothiazine, phenoxazine, pyrazole, indazole, imidazole, benzimidazole, naphthimidazole, phenanthrimidazole, pyridimidazole, pyrazineimidazole, quinoxalineimidazole, oxazole, benzoxazole, naphthoxazole, anthroxazole, phenanthroxazole, isoxazole, 1,2-thiazole, 1,3-thiazole, benzothiazole, pyridazine, benzopyridazine, pyrimidine, benzpyrimidine, quinoxaline, 1,5-diazaanthracene, 2,7-diazapyrene, 2,3-diazapyrene, 1,6-diazapyrene, 1,8-diazapyrene, 4,5-diazapyrene, 4,5,9,10-tetraazaperylene, pyrazine, phenazine, phenoxazine, phenothiazine, fluorubine, naphthyridine, azacarbazole, benzocarboline, phenanthroline, 1,2,3-triazole, 1,2,4-triazole, benzotriazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole, 1,2,4,5-tetrazine, 1,2,3,4-tetrazine, 1,2,3,5-tetrazine, purine, pteridine, indolizine and benzothiadiazole.
In a preferred embodiment of the invention R is a group of the formula (2).
Preference is given to the compounds of the formula (1) for which:
Particular preference is given to compounds of the formula (1) for which:
This preference applies in particular when the compound of the formula (1) is used as a blue-emitting dopant. In other functions, in the organic electronic device another selection of the groups may be preferred, especially of the A and Z groups.
Preference is further given to compounds of the formula (1) in which all symbols X represent the same aromatic or heteroaromatic system, more preferably benzene or naphthalene, most preferably benzene. Particular preference is also given to all symbols X having identical substitution.
Preference is likewise given to compounds of the formula (1) in which all symbols Y represent the same aromatic or heteroaromatic system, more preferably benzene or naphthalene, most preferably benzene. Particular preference is also given to all symbols Y having identical substitutions.
Preference is further given to compounds of the formula (1) in which all units Z are each selected identically and also bond to the same positions on X and Y in each case.
Particular preference is given to compounds of the formula (1), which have a symmetrical structure and which have a threefold rotational axis, especially those in which all units X and all units Y and Z and all substituents R1 and R2 are each selected identically.
These preferences arise in particular from the easier synthetic obtainability of the symmetrically structured compounds. However, more complicated synthetic methods in principle also make obtainable the unsymmetrically substituted compounds.
Preference is further given to the compounds of the formula (1) which have no benzylic protons. This applies in particular to radicals on the Z group. When the Z group is C(R1)2 or O(R1)2—C(R1)2, R1 is thus preferably not H. The reason for this preference is the comparatively high reactivity of benzylic protons so that the presence of benzylic protons might possibly lead to undesired side reactions in device production and operation.
A particularly preferred embodiment of the invention is that of compounds of the formula (3)
where A, Z, R1 and a are each defined as described above, where the maximum number of substituents R1 corresponds to the number of substitutable hydrogen atoms.
For particularly preferred compounds of the formula (3), the same preferences for the symbols A and Z apply as detailed above for compounds of the formula (1).
Examples of preferred compounds of formula (1) or formula (3) are the structures (1) to (30) depicted below, which may be substituted by R1 or unsubstituted.
A very particularly preferred embodiment of the invention is that of compounds of the formulae (4), (5), (6), (7), (8), (9), (10), (11) and (12)
In these compounds, the substituents Ra, Rb and Rc are preferably selected from the substituents as listed in Table 1. These preferred substituent combinations apply to all of the compounds of the formula (4) to formula (12).
The invention further provides for the use of compounds of the formula (1) or formula (3) in organic electronic devices, in particular in organic electroluminescent devices.
The invention further provides organic electroluminescent devices comprising cathode, anode and at least one emitting layer, characterized in that at least one organic layer comprises at least one compound of the formula (1) or formula (3).
Apart from the emitting layer, the organic electroluminescent device may comprise further layers. These may, for example, be: hole injection layer, hole transport layer, hole blocking layer, electron transport layer and/or electron injection layer. However, it should be pointed out here that not necessarily each of these layers has to be present. For instance, especially when compounds of the formula (1) or formula (3) are used as a dopant with electron-conducting host materials, very good results are is still obtained when the organic electroluminescent device does not contain any separate electron transport layer and the emitting layer directly adjoins the electron injection layer or the cathode. It may likewise be preferred when the organic electroluminescent device does not contain any separate hole transport layer and the emitting layer directly adjoins the hole injection layer or the anode. It may further be preferred when the compound of the formula (1) or formula (3) is used not only as the dopant in the emitting layer, but also additionally as a hole-conducting compound (as a pure substance or as a mixture) in the hole transport layer.
The compound of the formula (1) or formula (3) can perform different functions in the organic electroluminescent device. These depend upon the precise structure of this compound. Especially the selection of the A and Z groups determines the particularly suitable function of these compounds. For instance, these compounds can be used in particular as emitters, as hole transport materials, as electron transport materials, or, in electrophosphorescent devices, also as matrix materials or as hole blocking materials.
Suitable emitters are in particular compounds in which the symbols A and Z are:
Suitable hole transport materials are in particular compounds in which the symbols A and Z are:
Suitable electron transport materials for fluorescent or phosphorescent devices are in particular compounds in which the symbols A and Z are
Suitable matrix materials and hole blocking materials for electrophosphorescent devices are in particular compounds in which the symbols A and Z are:
When the compound of the formula (1) or formula (3) is used as an emitter, it is preferably used together with a host material. The proportion of the compound of the formula (1) or formula (3) in the mixture is then between 0.1 and 99% by weight, preferably between 0.5 and 50% by weight, more preferably between 1 and 20% by weight, in particular between 1 and 10% by weight. Correspondingly, the proportion of the host material in the mixture is between 1 and 99.9% by weight, preferably between 50 and 99.5% by weight, more preferably between 80 and 99% by weight, in particular between 90 and 99% by weight.
Preference is further given to organic electroluminescent devices, characterized in that a plurality of emitting compounds are used in the same layer or in different layers, of which at least one of these compounds has a structure of the formula (1). More preferably, these compounds together have a plurality of emission maxima between 380 nm and 750 nm, so that white emission results overall, i.e. apart from the compound of the formula (1) at least one further emitting compound which fluoresces or phosphoresces and which emits yellow, orange or red light is also used.
Preferred host materials are organic compounds, whose emission is at a shorter wavelength than that of the compound of the formula (1) or which do not emit at all in the visible region. Useful host materials are various substance classes. Preferred host materials are selected from the classes of the oligoarylenes (for example 2, 2′,7,7′-tetraphenylspirobifluorene according to EP 676461 or dinaphthylanthracene), of the atropisomers (for example according to the unpublished application EP 04026402.0, of the oligoarylenevinylenes (for example DPVBi or spiro-DPVBi according to EP 676461), of the polypodal metal complexes (for example according to WO 04/081017), of the hole-conducting compounds (for example according to WO 04/058911) or of the electron-conducting compounds, in particular ketones, phosphine oxides and sulphoxides (for example according to the unpublished patent application DE 102004008304.5). Particularly preferred host materials are selected from the classes of the oligoarylenes, including naphthalene, anthracene and/or pyrene, of the oligoarylenevinylenes, of the ketones, of the phosphine oxides and of the sulphoxides.
When the compound of the formula (1) or formula (3) is used, as a hole transport material, electron transport material or as a hole blocking material, it is preferred when this compound is used as the pure substance. Especially as a hole transport material and as an electron transport material, these compounds are also suitable for use in further organic electronic devices, for example in organic transistors.
When the compound of the formula (1) or formula (3) is used as a matrix material for electrophosphorescent devices, its proportion in the mixture is between 1 and 99.9% by weight, preferably between 30 and 99.5% by weight, more preferably between 50 and 99% by weight, in particular between 80 and 99% by weight. Correspondingly, the proportion of the emitter which emits light from the triplet state and therefore exhibits electrophosphorescence in the mixture is between 0.1 and 99% by weight, preferably between 0.5 and 70% by weight, more preferably between 1 and 50% by weight, in particular between 1 and 20% by weight.
The mixing ratios can be adjusted by mixing in solvents (or solvent mixtures) or by co-evaporation under reduced pressure, in a carrier gas stream or under vacuum.
Preference is further given to an organic electroluminescent device, characterized in that one or more layers are applied by a sublimation process. In this process, the materials are applied by vapour deposition in vacuum sublimation units at a pressure of less than 10−5 mbar, preferably less than 10−6 mbar, more preferably less than 10−7 mbar.
Preference is likewise given to an organic electroluminescent device, characterized in that one or more layers are applied by the OVPD (Organic Vapour Phase Deposition) process or with the aid of carrier gas sublimation. In this process, the materials are applied at a pressure between 10−5 mbar and 1 bar.
Preference is further given to an organic electroluminescent device, characterized in that one or more layers are produced from solution, for example by spin-coating, or by any printing process, for example screenprinting, flexographic printing or offset printing, but more preferably LITI (Light Induced Thermal Imaging, thermal transfer printing) or inkjet printing.
The above-described compounds in organic electronic devices have the following surprising advantages over the prior art:
The present application text and also the examples which follow below are aimed at the use of inventive compounds in relation to OLEDs and the corresponding displays. In spite of this restriction of the description, it is possible for those skilled in the art without any further inventive activity also to utilize the inventive compounds for further uses in other electronic devices, for example for organic field-effect transistors (O-FETs), organic thin-film transistors (O-TFTs), organic integrated circuits (O-ICs), organic solar cells (O-SCs), organic light-emitting transistors (O-LETs), organic field-quench devices (O-FQDs), light-emitting electrochemical cells (LECs) or else organic laser diodes (O-Laser), to name just a few applications. The use of the inventive compounds in the corresponding devices, just like these devices themselves, likewise form part of the subject-matter of the present invention. The invention is also given here in detail by the examples which follow without any intention to restrict it thereto
The syntheses which follow were, unless stated otherwise, carried out under a protective gas atmosphere. The reactants were purchased from Aldrich. Tris(p-bromophenyl)amine was synthesized according to J. Am. Chem. Soc. 1987, 109, 4960-4968. 2-Indenylboronic acid was synthesized according to J. Org. Chem. 2002, 67, 169-176; 2-bromobenzyl diethylphosphonate was synthesized according to Z. Anorg. Allg. Chem. 1994, 620(12), 2041-7.
800 mg (0.72 mmol) of Pd(PPh3)4 are added to a nitrogen-saturated mixture of 15.0 g (31 mmol) of tris(p-bromophenyl)amine, 19.8 g (124 mmol) or 2-indenylboronic acid, 40.0 g (188 mmol) of K3PO4, 1 l of dioxane and 1 l of water. The suspension is heated to 80° C. for 7 h. Afterwards, 0.09 g of NaCN is added and the aqueous phase is removed. The organic phase is washed twice with H2O and subsequently dried over Na2SO4. After the removal of the solvents and repeated recrystallization from toluene, yellow needles are obtained which, by HPLC, have a purity of approximately 99.9%. The yield is 16 g (88%).
1H NMR (CDCl3, 500 MHz): δ [ppm]=3.78 (s, 6H), 7.13-7.19 (m, 12H), 7.23-7.28 (m, 3H), 7.38 (d, J=7.4 Hz, 3H), 7.46 (d, J=7.4 Hz, 3H), 7.56 (d, J=8.7 Hz, 6H).
4.8 g (200 mmol) of sodium hydride are added in portions to a mixture of 33.2 g (55 mmol) of 4,4′,4″-tris(1H-inden-2-yl)triphenylamine and 300 ml of dimethylformamide. Subsequently, the suspension is heated to 80° C., admixed dropwise at this temperature with 18.7 ml (300 mmol) of methyl iodide and subsequently stirred at 80° C. for a further 50 h. Afterwards, the mixture is admixed at room temperature with 100 ml of ammonia solution and 500 ml of ethyl acetate, and the aqueous phase is removed. The organic phase is washed 5 times with 300 ml of water and subsequently dried over Na2SO4. After the removal of the solvent and repeated recrystallization from toluene (1.5 ml/g), yellow needles are obtained which, by HPLC, have a purity of 99.8%. The yield is 23.7 g (60.3%). The sublimation was effected at a pressure of approx. 5×10−5 mbar and T=300 C.
1H NMR (CDCl3, 500 MHz): δ [ppm]=1.51 (s, 18H), 2.10 (s, 9H), 7.14-7.20 (m, 9H), 7.24-7.27 (m, 6H), 7.40 (d, 3H), 7.47 (d, 3H), 7.58 (m, 3H).
A mixture, cooled to 0° C., of 107.5 g (350 mmol) of 2-bromobenzyl diethylphosphonate and 1000 ml of DMF is admixed with 67.3 g (700 mmol) of sodium tert-butoxide and stirred for 30 min. This mixture is admixed with a solution of 29.6 g (90 mmol) of tris(4-formylphenyl)amine in 1000 ml of DMF at 0° C. over 30 min. and subsequently stirred at 0 C for a further 4 h. This mixture is then admixed with stirring with 250 ml of 2.5 N aqueous hydrochloric acid, subsequently with 600 ml of water and then with 200 ml of ethanol, and stirred for a further 30 min. The precipitate is filtered off with suction, washed twice with 200 ml each time of a mixture of water/ethanol (1:1, v:v) and three times with 200 ml each time of ethanol, and subsequently dried under reduced pressure. The solid thus obtained is recrystallized from 160 ml of DMF, finally extracted from 500 ml of hot ethanol by stirring and dried under reduced pressure.
The yield at a purity of 99.0% by 1H NMR is 51.0 g (65 mmol) corresponding to 71.8% of theory.
1H NMR (CDCl3, 500 MHz): δ [ppm]=7.66 (d, 3H), 7.58 (d, 3H), 7.47 (d, 6H), 7.39 (d, 3H), 7.30 (dd, 3H), 7.13 (d, 6H), 7.10 (dd, 3H), 7.01 (d, 3H).
An efficiently stirred suspension of 7.9 g (10 mmol) of tris(4-(2-bromophenylvinyl)phenyl)amine in 300 ml of diethyl ether is admixed at −78° C. dropwise with 14.4 ml (36 mmol) of n-butyllithium (2.5 molar in n-hexane). After stirring for a further 15 min., the cold bath is removed and the reaction mixture is allowed to warm to room temperature and subsequently stirred at room temperature for a further 3 h. The suspension is then admixed dropwise at room temperature with a solution of 7.2 g (40 mmol) of fluorenone in 200 ml of diethyl ether, and stirred at room temperature for a further 14 h. The yellow suspension is admixed with a mixture of 10 ml of acetic acid and 200 ml of water and stirred thoroughly for 30 min. The organic phase is removed, washed twice with 500 ml of water and concentrated to dryness. The solid is taken up in 500 ml of toluene, admixed with 1.0 g of p-toluenesulphonic acid and boiled on a water separator until no further water separates out (approx. 3 h). After cooling, the yellow solution is filtered through silica gel, the toluene is removed under reduced pressure, and the residue is recrystallized three times from DMF (10 ml/g) and five times from dioxane (10 ml/g).
The yield at a purity of 99.9% by 1H NMR is 5.1 g (4.9 mmol), corresponding to 49.2% of theory. The sublimation was effected at a pressure of approx. 5×10−5 mbar and T=380° C.
1H NMR (TCE-d2+1 μl of hydrazine hydrate, 500 MHz): δ [ppm]=7.81 (d, 6H, fluorene), 7.42 (s, 3H, H3), 7.40 (d, 3H, H4), 7.32 (dd, 6H, fluorene), 7.17 (dd, 3H, H5), 7.07 (dd, 6H, fluorene), 6.87 (dd, 3H, H6), 6.81 (d, 6H, fluorene), 6.76 (d, 6H, H2), 6.43 (d, 6H, H1), 6.38 (d, 3H, H7).
4,4′,4″-Tris(spiro(fluorene-9,1′-inden-2-yl)triphenylamine is oxidized in solution under air to the corresponding radical cation, recognizable by a high line broadening of the 1H NMR signals of the phenyl-indenyl part of the spectrum. The reduction to the amine can be effected, for example, with hydrazine hydrate (see 1H NMR spectrum). This redox reaction is reversible; no decomposition of the molecule can be observed even on repeated performance of the redox cycle.
An efficiently stirred suspension of 7.9 g (10 mmol) of tris(4-(2-bromophenylvinyl)-phenyl)amine in 300 ml of diethyl ether is admixed dropwise at −78° C. with 14.4 ml (36 mmol) of n-butyllithium (2.5 molar in n-hexane). After stirring for a further 15 min., the cold bath is removed, and the reaction mixture is allowed to warm to room temperature and subsequently stirred at room temperature for a further 3 h. The suspension is admixed dropwise at room temperature with a solution of 8.4 g (40 mmol) of 4,4′-dimethylbenzophenone in 200 ml of diethyl ether and stirred at room temperature for a further 14 h. The yellow suspension is admixed with a mixture of 10 ml of acetic acid and 200 ml of water and stirred thoroughly for 30 ml The organic phase is removed, washed twice with 500 ml of water and concentrated to dryness. The solid is taken up in 500 ml of toluene, admixed with 1.0 g of p-toluenesulphonic acid and boiled on a water separator until no further water separates out (approx. 3 h). After cooling, the yellow solution is filtered through silica gel, the toluene is removed under reduced pressure and the residue is recrystallized three times from DM F (10 ml/g) and five times from dioxane (8 ml/g).
The yield at a purity of 99.9% by 1H NMR is 5.9 g (5.2 mmol), corresponding to 51.4% of theory. The sublimation was effected at a pressure of approx. 5×10−5 mbar and T=370 C.
1H NMR (TCE-d2+1 μl of hydrazine hydrate, 500 MHz): δ [ppm]=7.40 (s, 3H, H3), 7.38 (d, 3H, H4), 7.20 (m, 12H, AB-p-tolyl), 7.19 (dd, 3H, H5), 6.89 (dd, 3H, H6), 6.76 (d, 6H, H2), 6.62 (m, 12H, AB-p-tolyl), 6.37 (d, 6H, H1), 6.36 (d, 3H, H7), 2.41 (s, 18H, CH3).
4,4′,4″-Tris(1,1′-di-para-tolyl-inden-2-yl)triphenylamine is oxidized in solution under air to the corresponding radical cation, recognizable by a high line broadening of the 1H NMR signals of the phenyl-indenyl part of the spectrum. The reduction to the amine can be effected, for example, with hydrazine hydrate (see 1H NMR spectrum). This redox reaction is reversible; no decomposition of the molecule is observed, even on repeated performance of the redox cycles.
A mixture, cooled to 0° C., of 51.9 g (50 mmol) of 4,4′,4″-tris(spiro(fluorene-91′-inden-2-yl)triphenylamine (synthesized according to Example 3) dissolved in 1000 ml of dichloromethane is admixed with exclusion of light at 0° C. with a mixture of 2.6 ml (50 mmol) of bromine and 100 ml of dichloromethane, and stirred at 0° C. for 4 h. After the dichloromethane has been removed under reduced pressure, the residue is washed with a little ethanol, recrystallized once from toluene and dried under reduced pressure. The yield, at a purity of about 97.0% by HPLC, is 69.4 g (46 mmol), corresponding to 91.5% of theory.
An efficiently stirred suspension of 40.0 g (26 mmol) of 4,4′,4″-tris[2,3-dibromo-spiro(fluorene-9,1′-inden-2-yl)]triphenylamine in 300 ml THF is admixed in portions at 0 C with 5.1 g (45 mmol) of potassium tert-butoxide and stirred at room temperature for 1 h. Subsequently, the mixture is poured into 100 ml of ice-water and extracted three times with 200 ml each time of dichloromethane, and the dichloromethane phase is washed three times with 300 ml of water, and once with 300 ml of saturated NaCl solution, and then dried over sodium sulphate. After the solvent has been removed under reduced pressure, the residue is recrystallized from DMF. The yield, at a purity of about 98.0% by HPLC, is 28.7 g (22.5 mmol) corresponding to 85.4% of theory.
An efficiently stirred suspension of 12.8 g (10 mmol) of 4,4′,4″-tris[3-bromo-spiro(fluorene-1′,9-1H-inden-2-yl)]triphenylamine in 300 ml of diethyl ether is admixed dropwise at −78° C. with 14.4 ml (36 mmol) of n-butyllithium (2.5 molar in n-hexane). After stirring for a further 15 min., the cold bath is removed, and the reaction mixture is allowed to warm to room temperature and subsequently stirred at room temperature for a further 3 h. The suspension is then admixed dropwise at room temperature with a solution of 7.9 g (44 mmol) of fluorenone in 200 ml of diethyl ether, and stirred at room temperature for a further 14 h. The yellow suspension is admixed with a mixture of 10 ml of acetic acid and 200 ml of water, and stirred thoroughly for 30 min. The organic phase is removed, washed twice with 500 ml of water and concentrated to dryness. The solid is taken up in 500 ml of toluene, admixed with 500 mg of p-toluenesulphonic acid and boiled on a water separator until no further water separates out (approx. 3 h). After cooling, the yellow solution is filtered through silica gel, the toluene is removed under reduced pressure and the residue is recrystallized three times from DMF (15 ml/g) and five times from dioxane (12 ml/g). The yield at a purity of 99.9% by 1H NMR is 7.5 g (4.9 mmol) corresponding to 49.2% of theory. The sublimation was effected at a pressure of approx. 5×10−5 mbar and T=395° C.
1H NMR (TCE-d2+1 μl of hydrazine hydrate, 500 MHz): δ [ppm]=7.81 (d, 6H, fluorene), 7.77 (d, 6H, fluorene), 7.40 (d, 3H), 7.32 (dd, 6H, fluorene), 7.30 (dd, 6H, fluorene), 7.17 (dd, 3H), 7.09 (d, 3H), 7.07 (dd, 6H, fluorene), 7.01 (dd, 6H, fluorene), 6.87 (dd, 3H), 6.85 (d, 6H, fluorene), 6.80 (d, 6H, fluorene), 6.66 (dd, 3H), 6.46 (dd, 3H), 6.38 (d, 3H), 6.28 (d, 3H).
4,4′,4″-Tris[5,5,10,10-di-spiro-fluorenyl-5,10-dihydroindeno[2,1-a]inden-2-yl]amine is oxidized in solution under air to the corresponding radical cation, recognizable by a high line broadening of the 1H NMR signals of the phenyl-indenyl part of the spectrum. The reduction to the amine can be effected, for example, with hydrazine hydrate (see 1H NMR spectrum). This redox reaction is reversible; no decomposition of the molecule is observed, even on repeated performance of the redox cycle.
OLEDs are produced by a general process according to WO 04/058911, which is adapted in the individual case to the particular circumstances (for example layer thickness variation in order to achieve optimal efficiency and colour).
In the Examples 7 to 11 which follow, the results of various OLEDs are presented. The fundamental structure, the materials and layer thicknesses used, apart from the emitting layer and electron transport layer, are identical in Examples 7 to 10 for better comparability. Analogous to the abovementioned general process, OLEDs with the following structure are obtained (except that the hole transport layer detailed below is not relevant for Example 7):
In Example 7 the hole transport materials used, apart from the two mentioned above, are NPB (N-naphthyl-N-phenyl-4,4′-diaminobiphenyl) and HTM1 (2,2′,7,7′-tetrakis(di-para-tolylamino)spiro-9,9′-bifluorene).
These OLEDs which are yet to be optimized are characterized in a standard manner; for this purpose, the electroluminescence spectra, the efficiency (measured in cd/A), the power efficiency (measured in Im/W) as a function of brightness, calculated from current-voltage-brightness characteristics (IUL characteristics), and the lifetime are determined. The lifetime is defined as the time after which the starting brightness of the OLED has fallen by half at a constant current density of 10 mAcm2.
Table 1 then summarizes the results of some OLEDs (Examples 7 to 10) with the composition of the EML and the ETL including the layer thicknesses also being listed in each case. The emitting layers comprise, as emitting materials of the formula (1), the dopant D1 (according to structure Example 1). The comparative examples used are OLEDs which comprise, as emitting compounds, the dopant D2 according to the abovementioned prior art or only the host material. The host materials used are the compounds H1 to H4 depicted below. The electron transport materials used are ETM1 (AlQ3, purchased from SynTec, tris(quinolinato)aluminium(III)) or E™2 bis(9,9′-spirobifluoren-2-yl)phenylphosphine oxide according to WO 05/003253). Table 2 summarizes the results of further OLEDs (Example 11) which comprises, as emitting materials of the formula (1), the dopant D1 or the dopant D3 and which have been optimized for better efficiency and lifetime by variation of the hole transport layers.
For better clarity, the corresponding structural formulae of the dopants and host materials used are shown below:
| Number | Date | Country | Kind |
|---|---|---|---|
| 04028407.7 | Dec 2004 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP05/12807 | 12/1/2005 | WO | 00 | 5/31/2007 |
