Patent Application
20220275009
The addition of hydrosilicon compounds to unsaturated organic compounds such as alkenes and alkynes plays an important role in technology. This reaction, referred to as hydrosilylation, is used, for example, to crosslink siloxanes and to introduce functional groups into silanes or siloxanes. In general, hydrosilylations only proceed catalyzed. In the prior art, primarily platinum, rhodium or iridium complexes are used as catalysts, which make the process considerably more expensive. In addition, noble metals are only available to a limited extent as raw materials and are subject to price fluctuations that cannot be foreseen or influenced. Noble metal-free catalyst systems are therefore of great technical interest for hydrosilylations.
It is known from WO2017/174290 that cationic silicon(II) compounds catalyze hydrosilylations.
Angew. Chem. Int. Ed. 2017, 56, 1365 describes the hydrosilylation of trifluoroacetophenone and of CO2 in the presence of a heterocyclic germylene donor-stabilized by phosphorus and nitrogen moities, which has an electrically neutral germanium center. In these compounds, the phosphorus center represents the catalysis center, which activates the silicon-hydrogen compound for the hydrosilylation process.
One problem with the noble metal-free catalysts described above is that they are extremely sensitive to air and moisture. Their use therefore requires special measures that ensure exclusion of air and moisture. This increases the technical complexity involved in their production and use. In addition, they or their precursors are only accessible via complex, multi-stage syntheses and are therefore not technically widely applicable.
It was therefore an object of the present invention to provide compounds as catalysts for hydrosilylation which do not have the disadvantages of the catalysts known to date.
A further object of the present invention was to provide novel mixtures which can hydrosilylate.
It has been found that cationic germanium(II) compounds catalyze hydrosilylations in the presence of oxygen.
It has also been found that cationic germanium(II) compounds are stable as solids in air for several days. This is surprising since the corresponding silicon(II) compounds decompose very rapidly in air. The germanium(II) compounds according to the invention constitute a considerable technical advantage.
Some germanium(II) compounds with inorganic anions and a method for the preparation thereof have already been described by Jutzi et al. in Organometallics 1986, 5, 730. Cp*Ge+ BF4− is obtained in 54% yield by reacting pentamethylcyclopentadienylgermanium chloride with HBF4 at −80° C., Cp*Ge+ AlCl4− is obtained in 42% yield by reacting pentamethylcyclopentadienylgermanium chloride with aluminum trichloride, and Cp*Ge+ GeCl3− is obtained in 92% yield by reacting pentamethylcyclopentadienylgermanium chloride with germanium dichloride-dioxane complex. However, these access routes are very specific and cationic germanium(II) compounds with organic anions are not accessible in this manner. A general, simple strategy with which a wide number of different compounds may be prepared, in particular those having an organic anion, is thus currently unknown.
It was therefore a further object of the present invention to provide a method with which a large number of cationic germanium(II) compounds are accessible in a simple manner.
The stated objects are achieved by the subject matter of the patent claims.
The present invention relates to a mixture M
comprising
(a) at least one compound A selected from
(a1) a compound of the general formula (I)
R1R2R3Si—H (I),
in which the radicals R1, R2 and R3 are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, where two of the radicals R1, R2 and R3 may also form with each other a monocyclic or polycyclic, unsubstituted or substituted C2-C20-hydrocarbon radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen, —C≡N, —ORz, —SRz, —NRz2, —PRz2, —O—CO—Rz, —NH—CO—Rz, —O—CO—ORz or —COORz, a CH2 group can be replaced by —O—, —S— or —NRz—, and a carbon atom can be replaced by a Si atom, in which Rz is in each case independently selected from the group consisting of hydrogen, C1-C6-alkyl radical, C6-C14-aryl radical, and C2-C6-alkenyl radical; and/or
(a2) a compound of the general formula (I′)
(SiO4/2)a(RxSiO3/2)b(HSiO3/2)b′(Rx2SiO2/2)c(RxHSiO2/2)c′(H2SiO2/2)c″(Rx3SiO1/2)d(HRx2SiO1/2)d′(H2RxSiO1/2)d″(H3SiO1/2)d′″ (I′),
in which the radicals Rx are each independently selected from the group consisting of (i) halogen, (ii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iii) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, where substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen, a CH2 group can be replaced by —O— or —NRz—, in which Rz is in each case independently selected from the group consisting of hydrogen, C1-C6-alkyl radical, C6-C14-aryl radical, and C2-C6-alkenyl radical; and in which the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ specify the number of the respective siloxane unit in the compound and are each independently an integer in the range from 0 to 100 000, with the proviso that the sum of a, b, b′, c, c′, c″, d, d′, d″, d′″ together has the value of at least 2 and at least one of the indices b′, c′, c″, d′, d″ or d′″ is not equal to 0; and
(b) at least one compound B selected from
(b1) a compound of the general formula (II)
R4R5C═CR6R7 (II), and/or
(b2) a compound of the general formula (II′)
R8C≡CR9 (II′),
in which the radicals R4, R5, R6, R7, R8 and R9 are each independently selected from the group consisting of (i) hydrogen, (ii) —C≡N, (iii) organosilicon radical having 1-100 000 silicon atoms, (iv) unsubstituted or substituted C1-C20-hydrocarbon radical, and (v) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, where two of the radicals R4, R5, R6 and R7 may also form with each other a monocyclic or polycyclic, unsubstituted or substituted C2-C20-hydrocarbon radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen, —C≡N, —ORz, —SRz, —NRz2, —PRz2, —O—CO—R, —NH—CO—W, —O—CO—ORz, —COORz or —[O—(CH2)n]o—(CH(O)CH2) where n=1-6 and o=1-100, a CH2 group can be replaced by —O—, —S— or —NRz—, and a carbon atom can be replaced by a Si atom, in which Rz is in each case independently selected from the group consisting of hydrogen, C1-C6-alkyl, C6-C14-aryl, and C2-C6-alkenyl; and/or
(b3) a compound of the general formula (II″)
Rx3Si—O[—SiRx2—O]m—[Si(MB)Rx—O]n—SiRx3 (II″),
in which the radicals Rx are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) MB, (iv) unsubstituted or substituted C1-C20-hydrocarbon radical, and (v) unsubstituted or substituted C1-C20-hydrocarbonoxy radical;
and in which MB is each independently (i) —(CH2)o—CR═CR2 or (ii) —(CH2)o—C≡CR, where o=0-12 and in which R is in each case independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen, —C≡N, —ORz, —SRz, —NRz2, —PRz2, —O—CO—Rz, —NH—CO—Rz, —O—CO—ORz or —COORz, a CH2 group can be replaced by —O—, —S— or —NRz—, and a carbon atom can be replaced by a Si atom, in which Rz is in each case independently selected from the group consisting of hydrogen, C1-C6-alkyl radical, C6-C14-aryl radical, and C2-C6-alkenyl radical,
and in which m and n are each independently an integer in the range from 0 to 100 000, with the proviso that at least one radical MB is present in the compound; and
(c) at least one compound C selected from cationic germanium(II) compounds of the general formula (III)
([Ge(II)Cp]+)aXa− (III),
in which Cp is a π-bonded cyclopentadienyl radical of the general formula (IIIa)
in which the radicals Ry are each independently selected from the group consisting of (i) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-hydrocarbon radical, (ii) hydrogen, (iii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, wherein in each case two radicals Ry can also form with each other a monocyclic or polycyclic C2-C20-hydrocarbon radical, and wherein substituted means in each case that in the hydrocarbon or hydrocarbonoxy radical also at least one carbon atom can be replaced by a Si atom,
Xa− is an a valent anion; and
a can have the values 1, 2 or 3.
Compound A
At least one compound A is present in the mixture M, which also includes mixtures of compounds of the general formula (I) and/or mixtures of compounds of the general formula (I′).
In formula (I), the radicals R1, R2 and R3 are preferably each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) unsubstituted or substituted C1-C12-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C12-hydrocarbonoxy radical, wherein substituted has the same definition as before; and in formula (I′) the radicals Rx are preferably each independently selected from the group consisting of chlorine, C1-C6-alkyl radical, C2-C6-alkenyl radical, phenyl, and C1-C6-alkoxy radical, and the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ are each independently selected from an integer in the range of 0 to 1000.
In formula (I) the radicals R1, R2 and R3 are particularly preferably each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C1-C6-alkyl radical, (iv) C2-C6-alkenyl radical, (v) phenyl, and (vi) C1-C6-alkoxy radical; and in formula (I′) the radicals Rx are particularly preferably each independently selected from the group consisting of chlorine, methyl, methoxy, ethyl, ethoxy, n-propyl, n-propoxy, and phenyl, and the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ are each independently selected from an integer in the range from 0 to 1000.
In formula (I) the radicals R1, R2 and R3 and in formula (I′) the radicals Rx are especially preferably each independently selected from the group consisting of hydrogen, chlorine, methyl, methoxy, ethyl, ethoxy, n-propyl, n-propoxy, and phenyl, and the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ are preferably each independently selected from an integer in the range from 0 to 1000.
A mixture of compounds of the formula (I′) is present, particularly in the case of polysiloxanes. For the sake of simplicity, however, the individual compounds of the mixture are not specified for polysiloxanes, but an average formula (I′a) similar to the formula (I′) is given:
(SiO4/2)a(RxSiO3/2)b(HSiO3/2)b′(Rx2SiO2/2)c(RxHSiO2/2)c′(H2SiO2/2)c″(Rx3SiO1/2)d(HRx2SiO1/2)d′(H2RxSiO1/2)d″(H3SiO1/2)d′″ (I′a),
in which the radicals Rx have the same definition as in formula (I′), but the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ are each independently a number in the range of 0 to 100 000 and specify the average content of the respective siloxane unit in the mixture. Preference is given to those mixtures of the average formula (I′a), in which the indices a, b, b′, c, c′, c″, d, d′, d″, d′″ are each independently selected from a number in the range of 0 to 20 000.
Examples of compounds A of the general formula (I) are the following silanes (Ph=phenyl, Me=methyl, Et=ethyl): Me3SiH, Et3SiH, Me2PhSiH, MePh2SiH, Me2ClSiH, Et2ClSiH, MeCl2SiH, Cl3SiH, Me2(MeO)SiH, Me(MeO)2SiH, (MeO)3SiH, Me2(EtO)SiH, Me(EtO)2SiH, (EtO)3SiH; and examples of compounds A of the general formula (I′) are the following siloxanes and polysiloxanes:
HSiMe2-O—SiMe2H, Me3Si—O—SiHMe2, Me3Si—O—SiHMe-O—SiMe3,
H—SiMe2-(O—SiMe2)m-O—SiMe2-H, in which m is a number in the range of 1 to 20 000,
Me3Si—O—(SiMe2-O)n(SiHMe-O)o—SiMe3, in which n and o are each independently a number in the range of 1 to 20 000.
Compound B
At least one compound B is present in the mixture M, which also includes mixtures of compounds of the general formula (II) and/or mixtures of compounds of the general formula (II′) and/or mixtures of compounds of the general formula (II″).
Organosilicon radical in formula (II′) means a compound having at least one direct Si—C bond in the molecule.
In the formulae (II) and (II′) the radicals R4, R5, R6, R7, R8 and R9 are preferably each independently selected from the group consisting of (i) hydrogen, (ii) —C≡N, (iii) unsubstituted or substituted C1-C12-hydrocarbon radical, (iv) unsubstituted or substituted C1-C12-hydrocarbonoxy radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has one of the following substitutions: a hydrogen atom can be replaced by halogen, —C≡N, C1-C6-alkoxy, —NRz2, —O—CO—Rz, —NH—CO—Rz, —O—CO—ORz, —COORz or —[O—(CH2)n]o—(CH(O)CH2) where n=1-3 and o=1-20, in which Rz is in each case independently selected from the group consisting of hydrogen, chlorine, C1-C6-alkyl, C2-C6-alkenyl, and phenyl; and (v) organosilicon radical selected from the general formula (IIa),
(CH2)n—SiRx3 (IIa),
in which the radicals Rx are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen, a CH2 group can be replaced by —O— or —NRz—, in which Rz is selected from the group consisting of hydrogen, C1-C6-alkyl, C6-C14-aryl, and C2-C6-alkenyl;
and in which n=0-12;
and in formula (II″) the radicals Rx are preferably each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C1-C6-alkyl radical, (iv) phenyl, (v) MB and (vi) C1-C6-alkoxy radical, where MB is in each case independently (i) —(CH2)o—CR═CR2 or (ii) —(CH2)o—C≡CR, where o=0-6 and in which R is in each case independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C1-C6-alkyl radical, (iv) phenyl, and (v) C1-C6-alkoxy radical.
In the formulae (II) and (II′) the radicals R4, R5, R6, R7, R8 and R9 are particularly preferably each independently selected from the group consisting of (i) hydrogen, (ii) —C≡N, (iii) organosilicon radical selected from the general formula (IIa), in which the radicals Rx are each independently selected from the group consisting of hydrogen, chlorine, C1-C6-alkyl radical, C2-C6-alkenyl radical, phenyl and C1-C6-alkoxy radical; (iv) unsubstituted or substituted C1-C6-hydrocarbon radical, and (v) unsubstituted or substituted C1-C6-hydrocarbonoxy radical, wherein substituted means in each case that the hydrocarbon or hydrocarbonoxy radical has each independently at least one of the following substitutions: a hydrogen atom can be replaced by chlorine, —C≡N, —O—CH2—(CH(O)CH2) (=glycidoxy radical), —NRz2 and —O—CO—Rz, wherein Rz is in each case independently selected from the group consisting of hydrogen and C1-C6-alkyl;
and in formula (II″) the radicals Rx are particularly preferably each independently selected from the group consisting of C1-C3-alkyl radical and MB, where MB is in each case —(CH2)o—CR═CR2, in which R is in each case hydrogen and o=0-6.
Examples of compounds of the formula (II″) are
Rx3Si—O[—SiRx2—O]m—[Si(MB)2—O]1-100000—SiRx3,
Rx3Si—O[—SiRx2—O]m—[Si(MB)Rx—O]1-100000—SiRx3,
(MB)Rx2Si—O[—SiRx2—O]m—[Si(MB)Rx—O]n—SiRx3,
(MB)Rx2Si—O[—SiRx2—O]m—[Si(MB)2—O]n—SiRx3,
(MB)Rx2Si—O[—SiRx2—O]m—[Si(MB)Rx—O]n—SiRx2(MB),
(MB)Rx2Si—O[—SiRx2—O]m—[Si(MB)2—O]n—SiRx2(MB),
in which MB in each case is each independently (i) —(CH2)o—CR═CR2 or (ii) —(CH2)o—C≡CR, where o=0-12 and in which Rx, m and n have the same definition as in formula (II″).
Examples of compounds B are ethylene, propylene, 1-butylene, 2-butylene, isoprene, 1,5-hexadiene, cyclohexene, dodecene, cycloheptene, norbomene, norbornadiene, indene, cyclooctadiene,
styrene, α-methylstyrene, 1,1-diphenylethylene, cis-stilbene, trans-stilbene, 1,4-divinylbenzene, allylbenzene,
allyl chloride, allylamine, dimethylallylamine, acrylonitrile, allyl glycidyl ether, vinyl acetate, vinyl-Si(CH3)2OMe, vinyl-SiCH3(OMe)2, vinyl-Si(OMe)3,
vinyl-Si(CH3)2—O—[Si(CH3)2—O]n—Si(CH3)2-vinyl where n=0 to 10 000,
Me3Si—O—(SiMe2-O)n—[Si(vinyl)Me-O]O—SiMe3 where n=1 to 20 000 and o=1 to 20 000, acetylene, propyne, 1-butyne, 2-butyne and phenylacetylene.
In a particular embodiment, the compound A and the compound B are present in one molecule. Examples of such molecules are vinyldimethylsilane, allyldimethylsilane, vinylmethylchlorosilane and vinyldichlorosilane.
Compound C
Examples of radicals Ry in formula (III) are alkyl radicals, such as the methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, neopentyl and tert-pentyl radical; hexyl radicals such as the n-hexyl radical; heptyl radicals such as the n-heptyl radical; octyl radicals such as the n-octyl radical, and isooctyl radicals such as the 2,4,4-trimethylpentyl radical; nonyl radicals such as the n-nonyl radical; decyl radicals such as the n-decyl radical; dodecyl radicals such as the n-dodecyl radical; hexadecyl radicals such as the n-hexadecyl radical; octadecyl radicals such as the n-octadecyl radical; cycloalkyl radicals, such as the cyclopentyl, cyclohexyl, cycloheptyl radical and methylcyclohexyl radical; aryl radicals, such as the phenyl, naphthyl, anthracene and phenanthrene radical; alkaryl radicals, such as the o-, m- and p-tolyl, xylyl, mesitylenyl and o-, m- and p-ethylphenyl radical; alkaryl radicals, such as the benzyl radical, the α- and the β-phenylethyl radical; and alkylsilyl radicals such as trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyltert-butylsilyl and diethylmethylsilyl radical.
In formula (III), the radicals Ry are preferably each independently selected from the group consisting of (i) C1-C3-alkyl radical, (ii) hydrogen and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals. The radicals Ry are particularly preferably each independently selected from the methyl radical and trimethylsilyl radical. All radicals Ry are especially preferably a methyl radical.
The index a in formula (III) is preferably 1, so that X− is a monovalent anion.
Examples of anions X− are:
halides;
chlorate ClO4−;
tetrachlorometalates [MCl4]− where M=Al, Ga;
tetrafluoroborate [BF4]−;
trichlorometalates [MCl3]− where M=Sn, Ge;
hexafluorometalates [MF6]− where M=As, Sb, Ir, Pt; perfluoroantimonates [Sb2F11]−, [Sb3F16]− and [Sb4F21]−;
triflate (=trifluoromethanesulfonate) [OSO2CF3]−;
tetrakis(trifluoromethyl)borate [B(CF3)4]−; tetrakis(pentafluorophenyl) metalates [M(C6F5)4]−
where M=Al, Ga;
tetrakis(pentachlorophenyl)borate [B(C6Cl5)4]−;
tetrakis[(2,4,6-trifluoromethyl (phenyl)]borate {B[C6H2(CF3)3]}−;
[bis[tris(pentafluorophenyl)] hydroxide {HO[B(C6F5)3]2}−;
closo-carborates [CHB11H5Cl6]−, [CHB11H5Br6]−, [CHB11(CH3)5Br6]−, [CHB11F11]−, [C(Et)B11F11]−, [CB11(CF3)12] and B12Cl11N(CH3)3]−;
tetra(perfluoroalkoxy)aluminates [Al(ORPF)4]− where RPF=each independently perfluorinated C1-C14-hydrocarbon radical;
tris(perfluoroalkoxy)fluoroaluminates [FAl(ORPF)3]− where RPF=each independently perfluorinated C1-C14-hydrocarbon radical;
hexakis(oxypentafluorooxotellurato) antimonate [Sb(OTeF5)6]−;
borates and aluminates of the formulae [B(Ra)4]− and [Al(Ra)4]−, in which the radicals Ra are each independently selected from aromatic C6-C14-hydrocarbon radicals, in which at least one hydrogen atom has been mutually independently substituted by a radical selected from the group consisting of (i) fluorine, (ii) perfluorinated C1-C6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (III), the anions X— are preferably selected from the group consisting of the compounds of the formulae [B(Ra)4]− and [Al(Ra)4]−, in which the radicals Ra are in each case independently selected from aromatic C6-C14-hydrocarbon radicals in which at least one hydrogen atom has been mutually independently substituted by a radical selected from the group consisting of (i) fluorine, (ii) perfluorinated C1-C6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
Examples of radicals Ra are the m-difluorophenyl radical, 2,2,4,4-tetrafluorophenyl radical, perfluorinated 1-naphthyl radical, perfluorinated 2-naphthyl radical, perfluorobiphenyl radical, —C6F5, —C6H3(m-CF3)2, —C6H4(p-CF3), —C6H2(2,4,6-CF3)3, —C6F3(m-SiMe3)2, —C6F4(p-SiMe3), —C6F4(p-SiMe2t-butyl).
In formula (III), the anions X— are particularly preferably selected from the group consisting of the compounds of the formula [B(Ra)4]−, in which the radicals Ra are each independently selected from aromatic C6-C14-hydrocarbon radicals, in which all hydrogen atoms have been mutually independently substituted by a radical selected from the group consisting of (i) fluorine and (ii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (III), the anions X— are especially preferably selected from the group consisting of the compounds of the formula [B(Ra)4]−, in which the radicals Ra are each independently selected from the group consisting of —C6F5, perfluorinated 1- and 2-naphthyl radical, —C6F3(SiRb3)2 and —C6F4(SiRb3), in which the radicals Rb are in each case independently C1-C20-alkyl radicals.
In formula (III), the anions X— are most preferably selected from the group consisting of [B(C6F5)4]−, [B(C6F4(4-TBS)4]− where TBS=SiMe2tert-butyl, [B(2-NaphF)4]− where 2-NaphF=perfluorinated 2-naphthyl radical and [B(C6F5)3(2-NaphF)]− where 2-NaphF=perfluorinated 2-naphthyl radical.
Preferred compounds of the formula (III) are those in which all radicals Ry are methyl and the anions X— are selected from the group consisting of the compounds of the formulae [B(Ra)4]−, in which the radicals Ra are each independently selected from aromatic C6-C14-hydrocarbon radicals, in which at least one hydrogen atom has been mutually independently substituted by a radical selected from the group consisting of (i) fluorine, (ii) perfluorinated C1-C6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
The compounds of the formula (III) are particularly preferably selected from the group consisting of Cp*Ge+ B(C6F5)4−;
Cp*Ge+ B[C6F4(4-TBS)]4−, where TBS=SiMe2tert-butyl;
Cp*Ge+ B(2-NaphF)4−, where 2-NaphF=perfluorinated 2-naphthyl radical; and
Cp*Ge+ B[(C6F5)3(2-NaphF)]−, where 2-NaphF=perfluorinated 2-naphthyl radical.
The mixture M according to the invention may comprise any additional compounds such as processing aids, e.g. emulsifiers, fillers, for example highly dispersed silica or quartz, stabilizers, for example free radical inhibitors, pigments, for example dyes, or white pigments, for example chalk or titanium dioxide. The amounts of the further compounds are preferably between 0.1% by weight and 95% by weight, particularly preferably between 1% by weight and 80% by weight, very particularly preferably between 5% by weight and 30% by weight, based in each case on the total weight of the mixture M.
The invention further relates to a process for hydrosilylation of the mixture M according to the invention, wherein at least one compound A is reacted with at least one compound B in the presence of at least one compound C and in the presence of oxygen.
The amount of oxygen is not critical in the hydrosilylation; any oxygen-containing gas mixture known to those skilled in the art, such as ambient air, lean air, etc., can be used. The oxygen preferably originates from an oxygen-containing gas mixture having an oxygen content of 0.1-100% by volume.
It is also not critical when and how the oxygen is added. The oxygen-containing gas can, for example, be added once into the gas space, or it can be introduced continuously, or it can, prior to addition thereof, be passed over the cationic germanium(II) compound, or it can be introduced into a solution of the cationic germanium(II) compound, or it can be brought into contact with the reaction mixture via other methods known to those skilled in the art.
The reactants can be mixed with one another in any sequence, the mixing taking place in a manner known to those skilled in the art. For example, the compounds A, B and C can be mixed so that the hydrosilylation is initiated by contact with oxygen. It is also possible to first mix the compounds A and B or A and C or B and C and then to add the missing compound.
In a particular embodiment, the hydrosilylation of the mixture of the compounds A, B and C according to the invention is carried out under an air, lean air or oxygen atmosphere.
In a further particular embodiment, a solution of compound C is brought into contact with oxygen and mixed with compound A and compound B at a later point in time.
The molar ratio of the compounds A and B relative to the Si—H groups or unsaturated carbon moieties present, is typically in the range from 1:10 to 10:1, the molar ratio preferably being in the range from 1:5 to 5:1, particularly preferably in the range 1:2 to 2:1.
The molar ratio between the compound C and the Si—H groups present in the compound A is typically in the range from 1:107 to 1:1, preferably in the range from 1:106 to 1:10, particularly preferably in the range from 1:105 to 1:500.
The hydrosilylation can be carried out without solvent or with the addition of one or more solvents. The proportion of solvent or solvent mixture, based on the sum of the compounds A and B, is preferably in the range from 0.1% by weight up to 1000-fold the amount by weight, particularly preferably in the range from 10% by weight to 100-fold the amount by weight, very particularly preferably in the range from 30% by weight up to 10-fold the amount by weight.
Solvents used may preferably be aprotic solvents, for example hydrocarbons such as pentane, hexane, heptane, cyclohexane or toluene, chlorinated hydrocarbons such as dichloromethane, chloroform, chlorobenzene or 1,2-dichloroethane, ethers such as diethyl ether, methyl tert-butyl ether, anisole, tetrahydrofuran or dioxane, or nitriles such as for example acetonitrile or propionitrile.
The pressure in the hydrosilylation can be freely selected by those skilled in the art; it can be carried out under ambient pressure or under reduced or elevated pressure.
The pressure is preferably in a range from 0.01 bar to 100 bar, particularly preferably in a range from 0.1 bar to 10 bar, the hydrosilylation being especially preferably carried out at ambient pressure. If, however, compounds are involved in the hydrosilylation that are present in gaseous form at the reaction temperature, the reaction is preferably carried out at elevated pressure, particularly preferably at the vapor pressure of the overall system.
The person skilled in the art can freely select the temperature of the hydrosilylation. The hydrosilylation is typically carried out at a temperature in the range from −100° C. to +250° C., preferably in the range from −20° C. to +150° C., particularly preferably in the range from 0° C. to 100° C.
The invention further relates to cationic germanium(II) compounds of the formula (IV)
[Cp*Ge]+[B(Ra)4]− (IV),
in which Cp* is a π-bonded pentamethylcyclopentadienyl radical, and the radicals Ra are each independently selected from aromatic C6-C14-hydrocarbon radicals, in which at least one hydrogen atom has been mutually independently substituted by a radical selected from the group consisting of (i) fluorine, (ii) perfluorinated C1-C6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
Examples of radicals Ra in formula (IV) are the m-difluorophenyl radical, 2,2,4,4-tetrafluorophenyl radical, perfluorinated 1-naphthyl radical, perfluorinated 2-naphthyl radical, perfluorobiphenyl radical, —C6F, —C6H3(m-CF3)2, —C6H4(p-CF3), —C6H2(2,4,6-CF3)3, —C6F3(m-SiMe3)2, —C6F4(p-SiMe3), —C6F4(p-SiMe2t-butyl).
In formula (IV), the radicals Ra are preferably each independently selected from aromatic C6-C14-hydrocarbon radicals, in which all hydrogen atoms have been mutually independently substituted by a radical selected from the group consisting of (i) fluorine and (ii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (IV), the radicals Ra are especially preferably each independently selected from the group consisting of —C6F, perfluorinated 1- and 2-naphthyl radical, —C6F3(SiRb3)2 and —CF4(SiRb3), in which the radicals Rb are each independently C1-C6-alkyl radicals.
In formula (IV), the radicals Ra are most preferably each independently selected from the group consisting of —C6F, perfluorinated 2-naphthyl radical and —C6F4(4-SiMe2tert-butyl).
Preferred compounds of the formula (IV) are:
Cp*Ge+ B(C6F5)4−;
Cp*Ge+ B[C6F4(4-TBS)]4−, where TBS=SiMe2tert-butyl;
Cp*Ge+ B(2-NaphF)4−, where 2-NaphF=perfluorinated 2-naphthyl radical; and
Cp*Ge+ B[(C6F5)3(2-NaphF)]−, where 2-NaphF=perfluorinated 2-naphthyl radical.
The invention further relates to a method for preparing cationic germanium(II) compounds of the general formula (III)
([Ge(II)Cp]+)aXa− (III),
wherein
(a) a compound of the general formula (V)
[Cp2Ge(II)] (V),
in which the radicals Cp are each independently a π-bonded cyclopentadienyl radical of the general formula (Va)
in which the radicals Ry are each independently selected from the group consisting of (i) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals, (ii) hydrogen, (iii) unsubstituted or substituted C1-C20-hydrocarbon radical, and (iv) unsubstituted or substituted C1-C20-hydrocarbonoxy radical, wherein in each case two radicals Ry can also form with each other a monocyclic or polycyclic C2-C20-hydrocarbon radical, and wherein substituted means in each case that in the hydrocarbon or hydrocarbonoxy radical also at least one carbon atom can be replaced by a Si atom, with the proviso that in at least one Cp radical at least one radical Ry is a —CHR1R2 group, in which R1 and R2 are each independently selected from the group consisting of (i) hydrogen, (ii) C1-C19-alkyl radical and (iii) C6-C19-aryl radical; is reacted
with
(b) a carbocationic compound of the general formula (VI)
(Rd3C+)aXa− (VI),
in which a can take the values 1, 2 or 3;
and in which Xa− is an a valent anion;
and in which the radicals Rd are each independently selected from unsubstituted or substituted, aromatic C6-C14-hydrocarbon radicals, wherein substituted means that the hydrocarbon radical each independently has at least one of the following substitutions: a hydrogen atom can be replaced by halogen or C1-C6-alkyl radical
The index a in formula (VI) is preferably 1, so that X− is a monovalent anion.
In formula (VI), the anions X— are preferably selected from the group consisting of the compounds of the formula [B(Ra)4]−, in which the radicals Ra are in each case independently selected from aromatic C6-C14-hydrocarbon radicals in which at least one hydrogen atom has been mutually independently substituted by a radical selected from the group consisting of (i) fluorine, (ii) perfluorinated C1-C6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (VI), the anions X— are particularly preferably selected from the group consisting of compounds of the formula [B(Ra)4]−, in which the radicals Ra are each independently selected from aromatic C6-C14-hydrocarbon radicals, in which all hydrogen atoms have been mutually independently substituted by a radical selected from the group consisting of (i) fluorine and (ii) triorganosilyl radical of the formula —SiRb3, in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (VI), the anions X— are especially preferably selected from the group consisting of compounds of the formula [B(Ra)4]−, in which the radicals Ra are each independently selected from the group consisting of —C6F5, perfluorinated 1- or 2-naphthyl radical, —C6F3(SiRb3)2 and —C6F4(SiRb3), in which the radicals Rb are each independently C1-C20-alkyl radicals.
In formula (VI), the anions X— are most preferably selected from the group consisting of [B(C6F5)4]−, [B(C6F4(4-TBS)4]− where TBS=SiMe2tert-butyl, [B(2-NaphF)4]− where 2-NaphF=perfluorinated 2-naphthyl radical and [B(C6F5)3(2-NaphF)]− where 2-NaphF=perfluorinated 2-naphthyl radical.
In formula (VI), the radicals Rd are preferably each independently selected from the group consisting of unsubstituted phenyl or phenyl substituted by halogen atoms, tolyl, xylyl, mesitylenyl and ethylphenyl radical.
In formula (VI), the radicals Rd are particularly preferably each independently selected from the group consisting of phenyl, pentafluorophenyl, pentachlorophenyl, o-tolyl, m-tolyl, p-tolyl, xylyl, mesitylenyl, m-ethylphenyl, o-ethylphenyl and p-ethylphenyl radical.
Preferred compounds of the formula (VI) are those in which all radicals Rd are phenyl and the anions X− are selected from the group consisting of compounds of the formula [B(Ra)4]−, in which the radicals Ra are each independently selected from the group consisting of —C6F5, perfluorinated naphthyl radical and —C6F4(SiRb3), in which the radicals Rb are each independently C1-C20-alkyl radicals.
Examples of compounds of the formula (V) are:
decamethylgermanocene, decaisopropylgermanocene, and
octamethylbis(trimethylsilyl)germanocene, bis[(trimethylsilyl)cyclopentadienyl)] germanium,
bis[bis(trimethylsilyl)cyclopentadienyl] germanium,
bis[tris(trimethylsilyl]cyclopentadienyl]germanium.
Examples of compounds of the formula (VI) are:
(C6H5)3C+ B(C6F5)4−;
(C6H5)3C+ B[C6F4(4-TBS)]4−, where TBS=SiMe2tert-butyl;
(C6H5)3C+ B(2-NaphF)4−, where 2-NaphF=perfluorinated 2-naphthyl radical; and
(C6H5)3C+ B[(C6F5)3(2-NaphF)]−, where 2-NaphF=perfluorinated 2-naphthyl radical.
The molar ratio of the compound of the general formula (V) and the carbocationic compound of the general formula (VI) is preferably at least 1:10 and at most 10:1, particularly preferably at least 1:5 and at most 5:1, especially preferably at least 1:3 and at most 3:1. The two components can be mixed in any sequence, the mixing being carried out in a manner known to those skilled in the art. The carbocationic compound of the general formula (VI) is preferably added to the compound of the general formula (V).
The reaction can be carried out in the presence of one or more further components, for example in the presence of a solvent or a mixture of two or more solvents. Either the compound of the general formula (V) or the carbocationic compound of the general formula (VI) or both components can be dissolved in a solvent or in a solvent mixture. The proportion of the solvent or solvent mixture relative to the sum of the compounds of the general formula (V) and (VI) is preferably at least 0.1% by weight and at most 1000-fold the weight, particularly preferably at least 10% by weight and at most 100-fold the weight, especially preferably at least 30% by weight and at most 10-fold the weight.
Solvents used may be, for example, hydrocarbons such as pentane, hexane, heptane, cyclohexane or toluene, chlorinated hydrocarbons such as dichloromethane, chloroform, chlorobenzene or 1,2-dichloroethane, ethers such as diethyl ether, methyl tert-butyl ether, anisole, tetrahydrofuran or dioxane, or nitriles such as acetonitrile or propionitrile.
The pressure in the reaction can be freely selected by those skilled in the art; it can be carried out under ambient pressure or under reduced or elevated pressure. The pressure is preferably not less than 0.01 bar and not more than 100 bar, more preferably not less than 0.1 bar and not more than 10 bar; most preferably the reaction is carried out at ambient pressure.
The person skilled in the art can freely select the reaction temperature. The reaction is typically carried out at a temperature in the range from −100° C. to +250° C., preferably in the range from −20° C. to +150° C., particularly preferably in the range from 0° C. to +100° C.
In a particular embodiment, the cationic germanium(II) compound of the general formula (III) is generated in situ in compound A or in compound B or in a mixture of the two compounds A and B.
In this way there is no need to isolate the cationic germanium(II) compound. For a hydrosilylation reaction, this means a reduction in the number of reaction stages, since the reaction of the compound A with the compound B starts directly with the formation of the cationic germanium(II) compound, provided that oxygen is present.
The invention further relates to a catalyst system comprising at least one cationic germanium(II) compound of the general formula (III) and oxygen.
The invention further relates to the use of the cationic germanium(II) compounds of the formula (III) as a catalyst, especially as a catalyst for hydrosilylations.
Particular preference is given to the use of the cationic germanium(II) compounds of the formula (IV) as a catalyst.
The following tritylium salts were prepared analogously to the following literature references:
(C6H5)3C+ B[C6F4(4-TBS)]4−, TBS=SiMe2tert-butyl: Marks et al., Organometallics 1997, 16, 842-857).
Decamethylgermanocene: Weidenbruch et al., J. Organomet. Chem. 2006, 691, 809-810. (C6H5)3C+ B(NaphF)4− and (C6H5)3C+ B[(C6F4)3(Naph)]− where NaphF=perfluoro-ß-naphthyl: Mathur und Strickler, US 2015/0259362 (2017); Berris, WO2007/070770 (2007).
All steps were carried out under argon. 2.0 mg (2.3 μmol) of Cp*Ge B(C6F5)4− were dissolved in 801 mg of CD2Cl2 and added to a mixture of 238 mg (2.01 mmol) of α-methylstyrene and 303 mg (2.03 mmol) of 1,1,3,3,3-pentamethyldisiloxane and the mixture shaken. The solution was analyzed by 1H-NMR spectroscopy after 9 days. No hydrosilylation was detectable.
Under an argon atmosphere, 701 mg (2.04 mmol) of decamethylgermanocene (Cp*2Ge, Cp*=pentamethylcyclopentadienyl) were dissolved in 5 ml of dichloromethane and a solution of 1.70 g (1.83 mmol) of (C6H5)3C+ B(C6F5)4− in 5 ml of dichloromethane was added slowly at room temperature with shaking. Subsequently, enough heptane was added as precipitant until no further precipitation of the product took place. The supernatant solution was decanted off, the precipitate was redissolved in dichloromethane and again precipitated with heptane. The precipitated product was filtered off under suction and dried, finally under high vacuum.
Yield: 1.63 g (97%), pale pink solid.
1H-NMR (CD2Cl2): 6=2.23 (methyl groups).
13C-NMR (CD2Cl2): 6=8.82 (methyl groups), 6=123.1 (C's Cp*-Ring), 6=124 (broad), 6=135.3 (m), 6=137.3 (m), 6=139.2 (m), 6=147.2 (m), 6=149.1 (m): aromatic C—F.
11B-NMR (CD2Cl2): δ=−16.66 (s).
19F-NMR (CD2Cl2): δ=−167.4 (mc, 8 ortho-F), δ=−163.5 (mc, 4 para-F), δ=−132.9 (m, broad, 8 meta-F).
The crystalline solid was stored in air for 4 days and showed no visible change; the NMR spectrum was identical to that of the freshly prepared pure substance.
365.1 mg (0.279 mmol) of (C6H5)3C+ B[C6F4(4-TBS)]4− were dissolved in 965 mg of CD2Cl2 and the solution cooled to −30° C. 114.8 mg (0.335 mmol) of decamethylgermanocene (air-sensitive!) dissolved in ca. 350 mg of CD2Cl2 were slowly added under argon. The initially dark orange solution lightened to a pale yellowish color. 4 ml of pentane were added, the product precipitated as a beige solid and was washed with small portions of pentane. The solid was dried in vacuo. Yield: 300 mg (85%), beige solid.
1H-NMR (CD2Cl2): δ=0.352 (s, 2 Si—CH3), δ=0.913 s (Si-tert butyl), δ=2.17 (s, 15H, Cp*).
29Si-NMR (CD2Cl2): δ=5.63 (s, aromatic silyl group)
19F-NMR (CD2Cl2): δ=−132.2 (m, 8F), δ=−130.4 (m, 8F).
The preparation was carried out as in example 2 by reacting decamethylgermanocene with (C6H5)3C+ B(NaphF)4−.
Yield: 92%, beige solid.
1H-NMR (CD2Cl2): δ=2.22 (s, 15H, Cp*).
19F-NMR (CD2Cl2): δ=−161.3 to −160.9 (m, 4F), −159.8 to −159.4 (4F), −155.8 to −154.7 (4F), −150.2 to −149.8 (4F), −146.4 to −145.7 (4F), −125.9 to −124.4 (4F), −109.8 (mc, 1F), −109.3 (mc, 1F), −108.6 to −107.7 (m, 1F), −106.5 (mc, 1F).
11B-NMR (CD2Cl2): δ=−13.80.
The preparation was carried out as in example 2 by reacting decamethylgermanocene with (C6H5)3C+ B[(C6F4)3(NaphF)]−.
Yield: 70%, beige solid.
1H-NMR (CD2Cl2): δ=2.22 (s, 15H, Cp*).
11B-NMR (CD2Cl2): δ=−16.45.
207 mg (1.75 mmol) of α-methylstyrene and 229 mg (1.68 mmol) of dimethylphenylsilane together with 650 mg of CD2Cl2 were weighed into a reaction vessel under argon and 1.7 mg (1.92 μmol, 0.11 mol % based on dimethylphenylsilane) of Cp*Ge+ B(C6F5)4− in 160 mg CD2Cl2 were added. A syringe was used to inject 3 ml of air into the mixture. The reaction was complete after 24 hours at room temperature. This gave phenyl-CH(CH3)—CH2—Si(CH3)2Ph.
Product purity (GC)>90%,
1H-NMR (CD2Cl2): δ=0.43 and 0.49 (s, 2 CH3), δ=1.52 (mc, CH2), δ=1.56 (d, CH3), δ=3.20 (mc, CH), δ=7.40-7.50 (m, 3 aromatic H), δ=7.50-7.58 (m, 2 aromatic H), δ=7.59-7.66 (m, 3 aromatic H), δ=7.76-7.82 (m, 2 aromatic H).
120 mg (1.01 mmol) of α-methylstyrene and 137 mg (1.01 mmol) of dimethylphenylsilane together with 400 mg of CD2Cl2 were weighed into a reaction vessel under argon and 1.2 mg (0.94 μmol, 0.09 mol % based on dimethylphenylsilane) of Cp*Ge+ B(C6F5)4− in 130 mg CD2Cl2 were added. A syringe was used to inject 3 ml of air into the mixture. The reaction was complete after 24 hours at room temperature. This gave phenyl-CH(CH3)—CH2—Si(CH3)2Ph.
Product purity (GC)>90%,
1H-NMR (CD2Cl2): δ=0.43 and 0.49 (s, 2 CH3), δ=1.52 (mc, CH2), δ=1.56 (d, CH3), δ=3.20 (mc, CH), δ=7.40-7.50 (m, 3 aromatic H), δ=7.50-7.58 (m, 2 aromatic H), δ=7.59-7.66 (m, 3 aromatic H), δ=7.76-7.82 (m, 2 aromatic H).
1.7 mg (1.9 μmol) of Cp*Ge+ B(C6F5)4− were dissolved in 890 mg of CD2Cl2 and a total of ca. 0.6 ml (ca. 30 μmol) of oxygen was introduced at room temperature over a period of 15 minutes with exclusion of air. The solution was added to a mixture of 208 mg (1.76 mmol) of α-methylstyrene and 260 mg (1.75 mmol) of 1,1,3,3,3-pentamethyldisiloxane and the mixture was shaken. After 3 hours the conversion was ca. 35% and after 24 hours conversion was complete. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si (CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
1.7 mg (1.9 μmol) of Cp*Ge+ B(C6F5)4− were dissolved in 890 mg of CD2Cl2 and a total of ca. 8 ml (ca. 0.4 mmol) of oxygen was introduced at room temperature over a period of 3 hours with exclusion of air. The hydrosilylation was carried out as in Example 5. After 4 hours the conversion was ca. 83% and after 6 hours conversion was complete. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si (CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
1.6 mg (1.8 μmol) of Cp*Ge+ B(C6F5)4− were dissolved in 900 mg of CD2Cl2 and a total of ca. 1.2 ml (ca. 60 μmol) of oxygen were introduced at room temperature over a period of 30 minutes with exclusion of air. After a standing time of 23 hours, the hydrosilylation was carried out with this solution as in example 5. After 3 hours the conversion was ca. 65% and after 15 hours conversion was complete. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si (CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
299 mg (2.01 mmol) of pentamethyldisiloxane and 248 mg (2.10 mmol) of α-methylstyrene are mixed and a solution of 2.5 mg (2.03 μmol, 0.1 mol %) of Cp*Ge+ B(NaphF)4− in 361 mg of CD2Cl2 was added under argon. 1 ml of air is added 3 times in succession to the gas space above the solution and the mixture shaken for ca. 30 seconds each time. The hydrosilylation is monitored by 1H-NMR spectroscopy at room temperature. The conversion is 35% after 6 hours.
139 mg (1.66 mmol) of 1-hexene, 203 mg (1.37 mmol) of 1,1,3,3,3-pentamethyldisiloxane and 500 mg CD2Cl2 and a solution of 2.8 mg (3.16 μmol, 0.23 mol % based on 1,1,3,3,3-pentamethyldisiloxane) of Cp*Ge+ B(C6F5)4− in 170 mg CD2Cl2 were mixed in a reaction vessel under argon. 3 ml of air (ca. 0.8 mg of O2, corresponds to ca. 25 μmol) were added to the gas space using a syringe, the vessel sealed and heated at 45° C. for 4 hours. The gas chromatographic analysis showed a conversion of 90%. The main product of the reaction is CH3—(CH2)5—Si(CH3)2—O—Si(CH3)3. The identification was carried out by comparison with an authentic substance sample.
The working steps were carried out in air at room temperature.
815 mg (6.90 mmol) of α-methylstyrene and 1116 mg (7.52 mmol) of 1,1,3,3,3-pentamethyldisiloxane were mixed and 1.1 mg (0.865 mmol, 0.0125 mol % based on α-methylstyrene) of Cp*Ge+ B[C6F4(4-TBS)]4− were added. Conversion was complete after 24 hours. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si (CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
The working steps were carried out in air at room temperature.
805 mg (6.81 mmol) of α-methylstyrene and 1009 mg (6.80 mmol) of 1,1,3,3,3-pentamethyldisiloxane were mixed and a solution of 9.2 mg (7.23 μmol, 0.106 mol % based on 1,1,3,3,3-pentamethyldisiloxane) of Cp*Ge+ B[C6F4(4-TBS)]4− dissolved in 941 mg of CD2Cl2 was added with stirring. The mixture was diluted with a further 924 mg of CD2Cl2. After 3 hours the conversion was 91% and after 24 hours conversion was complete. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si(CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
After further addition of a mixture of 301 mg (2.55 mmol) of α-methylstyrene and 376 mg (2.53 mmol) of 1,1,3,3,3-pentamethyldisiloxane, the conversion was again complete after 24 hours, i.e. the product solution still contained active germanium(II) species.
After further addition of a mixture of 806 mg (6.82 mmol) of α-methylstyrene and 1003 mg (6.76 mmol) of 1,1,3,3,3-pentamethyldisiloxane, the conversion was again complete after 24 hours, i.e. the product solution still contained active germanium(II) species.
The working steps were carried out in air at room temperature.
801 mg (6.78 mmol) of α-methylstyrene and 1005 mg (6.78 mmol) of 1,1,3,3,3-pentamethyldisiloxane were mixed, 900 mg of CD2Cl2 were added and a solution of 0.9 mg (0.708 μmol, 0.010 mol % based on 1,1,3,3,3-pentamethyldisiloxane) of Cp*Ge+ B[C6F4(4-TBS)]4− dissolved in 922 mg of CD2Cl2 was added with stirring. The reaction was complete after 24 hours. The hydrosilylation product formed was phenyl —CH(CH3)—CH2—Si(CH3)2—O— Si(CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
In a glove box, under an argon atmosphere, 300 mg (2.02 mmol) of 1,1,3,3,3-pentamethyldisiloxane and 242 mg (2.05 mmol) of α-methylstyrene were mixed in an NMR tube and a solution of 1.9 mg (2.1 μmol) of Cp*Ge+ B(C6F5)4− in 807 mg of d8-toluene was added. After 9 days storage under argon, no reaction had taken place. The tube was opened and 1 ml of air (ca. 9 μmol of oxygen) was added. After 24 hours the conversion was 53% and after a further 3 days hydrosilylation was complete. The hydrosilylation product formed was phenyl —CH(CH3)—CH2—Si(CH3)2—O—Si(CH3)3, which was verified by means of 1H-NMR investigation in d8-toluene and comparison with an authentic sample.
The experiment according to Example 15 was repeated using CD2Cl2 instead of d8-toluene. After 9 days storage under argon, no reaction had taken place. The tube was opened and 1 ml of air (ca. 9 μmol of oxygen) was added. After 24 hours the conversion was 33% and after 2 days conversion was complete. The hydrosilylation product formed was phenyl-CH(CH3)—CH2—Si(CH3)2—O—Si(CH3)3, which was verified by means of 1H-NMR investigation in CD2Cl2 and comparison with an authentic sample.
150 mg (1.47 mmol) of phenylacetylene, 171 mg (1.47 mmol) of triethylsilane and 616 mg of CD2Cl2 were mixed in a reaction vessel under argon and a solution of 1.4 mg (1.58 μmol, 0.11 mol % based on reactants) of Cp*Ge+ B(C6F5)4− in 100 mg CD2Cl2 were added. 3 ml of air (ca. 0.8 mg of 02, corresponds to ca. 25 μmol) were added to the gas space using a syringe, the vessel sealed and heated at 50° C. for 40 hours. The following hydrosilylation products were detected in the specified proportions by gas chromatographic and GC/MS analysis: 60% Ph-CH═CH-SiEt3, 10% Ph-CH2—CH(SiEt3)2.
The reaction was carried out as in Example 17 at 50° C. with 103 mg (1.26 mmol) of 1-hexyne, 142 mg (1.22 mmol) of triethylsilane, 1.2 g of dichloromethane and 1.3 mg (1.41 μmol) of Cp*Ge+ B(C6F5)4− in 100 mg of CD2Cl2. The reaction time was 19 hours. Ca. 30% C4H9—CH═CH-SiEt3 were detected by gas chromatographic and GC/MS analysis.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/062003 | 5/10/2019 | WO |
