PREPARATION OF SILOXANES IN THE PRESENCE OF CATIONIC GERMANIUM(II) COMPOUNDS

Abstract

A mixture M includes at least one compound A selected from (a1) a compound of the general formula (I): R.sup.1R.sup.2R.sup.3Si—H, and/or (a2) a compound of the general formula (I′): (SiO.sub.4/2).sub.a(R.sup.xSiO.sub.3/2).sub.b(HSiO.sub.3/2).sub.b′(R.sup.x.sub.2SiO.sub.2/2).sub.c(R.sup.xHSiO.sub.2/2).sub.c′(H.sub.2SiO.sub.2/2).sub.c″(R.sup.x.sub.3SiO.sub.1/2).sub.d(HR.sup.x.sub.2SiO.sub.1/2).sub.d′(H.sub.2R.sup.xSiO.sub.1/2).sub.d″(H.sub.3SiO.sub.1/2).sub.d′″, and at least one compound B selected from (b1) a compound of the general formula (II): R.sup.4R.sup.5R.sup.6Si—O—R.sup.7, and/or (b2) a compound of the general formula (II′): R.sup.x.sub.3Si—O[—SiR.sup.x.sub.2—O].sub.m—[Si(OR.sup.7.sub.3)R.sup.x—O].sub.n—SiR.sup.x.sub.3, and at least one compound C selected from the cationic germanium(II) compound of the general formula (III): ([Ge(II)Cp].sup.+).sub.aX.sup.a−.

Claims

1-17. (canceled)

18. A mixture M, comprising: (a) at least one compound A selected from (a1) a compound of the general formula (I)
R.sup.1R.sup.2R.sup.3Si—H  (I), in which the radicals R.sup.1, R.sup.2 and R.sup.3 are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, and (iv) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbonoxy radical, where two of the radicals R.sup.1, R.sup.2 and R.sup.3 may also form with each other a monocyclic or polycyclic, unsubstituted or substituted C.sub.2-C.sub.20-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, —OR.sup.z, —SR.sup.z, —NR.sup.z.sub.2, —PR.sup.z.sub.2, —O—CO—R.sup.z, —NH—CO—R.sup.z, —O—CO—OR.sup.z or —COOR.sup.z, a CH.sub.2 group can be replaced by —O—, —S— or —NR.sup.z—, and a carbon atom can be replaced by a Si atom, in which R.sup.z is in each case independently selected from the group consisting of hydrogen, C.sub.1-C.sub.6-alkyl radical, C.sub.6-C.sub.14-aryl radical, and C.sub.2-C.sub.6-alkenyl radical; and/or (a2) a compound of the general formula (I′)
(SiO.sub.4/2).sub.a(R.sup.xSiO.sub.3/2).sub.b(HSiO.sub.3/2).sub.b′(R.sup.x.sub.2SiO.sub.2/2).sub.c(R.sup.xHSiO.sub.2/2).sub.c′(H.sub.2SiO.sub.2/2).sub.c″(R.sup.x.sub.3SiO.sub.2/2).sub.a(HR.sup.x.sub.2SiO.sub.1/2).sub.d(H.sub.2R.sup.xSiO.sub.1/2).sub.d″(H.sub.3SiO.sub.1/2).sub.d′″  (I′), in which the radicals R.sup.x are each independently selected from the group consisting of (i) halogen, (ii) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, and (iii) unsubstituted or substituted C.sub.1-C.sub.20-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 CH.sub.2 group can be replaced by —O— or —NR.sup.z—, in which R.sup.z is in each case independently selected from the group consisting of hydrogen, C.sub.1-C.sub.6-alkyl radical, C.sub.6-C.sub.14-aryl radical, and C.sub.2-C.sub.6-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)
R.sup.4R.sup.5R.sup.6Si—O—R.sup.7  (II), in which radicals R.sup.4, R.sup.5 and R.sup.6 are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, (iv) unsubstituted or substituted, 0-bonded or C-bonded C.sub.1-C.sub.20-hydrocarbonoxy radical, (v) organosilicon radical having 1-100 000 Si atoms, where two of the radicals R.sup.4, R.sup.5 and R.sup.6 may also form with each other a monocyclic or polycyclic, unsubstituted or substituted C.sub.2-C.sub.20-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, —OR.sup.z, —SR.sup.z—NR.sup.z.sub.2—PR.sup.z.sub.2, —O—CO—R.sup.z, —NH—CO—R.sup.z, —O—CO—OR.sup.z or —COOR.sup.z, a CH.sub.2 group can be replaced by —O—, —S— or —NR.sup.z—, and a carbon atom can be replaced by a Si atom, in which R.sup.z is in each case independently selected from the group consisting of hydrogen, C.sub.1-C.sub.6-alkyl radical, C.sub.6-C.sub.14-aryl radical, and C.sub.2-C.sub.6-alkenyl radical; and in which the radical R.sup.7 is selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.20-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, —OR.sup.z, —SR.sup.z, —NR.sup.z.sub.2, —PR.sup.z.sub.2, —O—CO—R.sup.z, —NH—CO—R.sup.z, —O—CO—OR.sup.z or —COOR.sup.z, a CH.sub.2 group can be replaced by —O—, —S— or —NR.sup.z—, and a carbon atom can be replace by a Si atom, in which R.sup.z is in each case independently selected from the group consisting of hydrogen, C.sub.1-C.sub.6-alkyl radical, C.sub.6-C.sub.14-aryl radical, and C.sub.2-C.sub.6-alkenyl radical; and/or (b2) a compound of the general formula (II′)
R.sup.x.sub.3Si—O[—SiR.sup.x.sub.2—O].sub.m—[Si(OR.sup.7.sub.3)R.sup.x—O].sub.n—SiR.sup.x.sub.3  (II′), in which the radicals R.sup.x are each independently selected from the group consisting of (i) hydrogen, (ii) halogen, (iii) —O—R.sup.7, (iv) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, and (v) unsubstituted or substituted, C-bonded C.sub.1-C.sub.20-hydrocarbonoxy radical; and in which the radicals R.sup.7 are in each case independently selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.20-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, —OR.sup.z, —SR.sup.z, —NR.sup.z.sub.2, —PR.sup.z.sub.2, —O—CO—R.sup.z, —NH—CO—R.sup.z, —O—CO—OR.sup.z or —COOR.sup.z, a CH.sub.2 group can be replaced by —O—, —S— or —NR.sup.z—, and a carbon atom can be replaced by a Si atom, in which R.sup.z is in each case independently selected from the group consisting of hydrogen, C.sub.1-C.sub.6-alkyl radical, C.sub.6-C.sub.14-aryl radical, and C.sub.2-C.sub.6-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 group —O—R.sup.7 is present in the compound; and (c) at least one compound C selected from the cationic germanium(II) compound of the general formula (III)
([Ge(II)Cp].sup.+).sub.aX.sup.a−  (III), in which Cp is a π-bonded cyclopentadienyl radical of the general formula (Ilia) ##STR00002## in which the radicals R.sup.y are each independently selected from the group consisting of (i) triorganosilyl radical of the formula —SiR.sup.b.sub.3, in which the radicals R.sup.b are each independently C.sub.1-C.sub.20-hydrocarbon radical, (ii) hydrogen, (iii) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbon radical, and (iv) unsubstituted or substituted C.sub.1-C.sub.20-hydrocarbonoxy radical, wherein in each case two radicals R.sup.y can also form with each other a monocyclic or polycyclic C.sub.2-C.sub.20-hydrocarbon radical, 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, X.sup.a− is an a valent anion; and a can have the values 1, 2 or 3.

19. The mixture M as claimed in claim 18, wherein in formula (I) the radicals R.sup.1, R.sup.2 and R.sup.3 are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) unsubstituted or substituted C.sub.1-C.sub.12-hydrocarbon radical, and (iv) unsubstituted or substituted C.sub.1-C.sub.12-hydrocarbonoxy radical, wherein substituted has the same definition as before; and in formula (I′) the radicals R.sup.x are each independently selected from the group consisting of chlorine, C.sub.1-C.sub.6-alkyl radical, C.sub.2-C.sub.6-alkenyl radical, phenyl, and C.sub.1-C.sub.6-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 1.

20. The mixture M as claimed in claim 19, wherein in formula (I) the radicals R.sup.1, R.sup.2 and R.sup.3 are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C.sub.1-C.sub.6-alkyl radical, (iv) C.sub.2-C.sub.6-alkenyl radical, (v) unsubstituted or substituted phenyl radical, and (vi) C.sub.1-C.sub.6-alkoxy radical; and in formula (I′) the radicals R.sup.x are 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.

21. The mixture M as claimed in claim 20, wherein in formula (I) the radicals R.sup.1, R.sup.2 and R.sup.3 and in formula (I′) the radicals R.sup.x are 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 each independently selected from an integer in the range from 0 to 1000.

22. The mixture M as claimed in claim 18, wherein in formula (II) the radicals R.sup.4, R.sup.5 and R.sup.6 are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) unsubstituted or substituted C.sub.1-C.sub.14-hydrocarbon radical, and (iv) unsubstituted or substituted, O-bonded or C-bonded C.sub.1-C.sub.14-hydrocarbonoxy radical, and the radical R.sup.7 is selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.6-hydrocarbon radical, and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.6-hydrocarbonoxy radical; and wherein in formula (II′) the radicals R.sup.x are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) —O—R.sup.7, (iv) unsubstituted or substituted C.sub.1-C.sub.14-hydrocarbon radical, and (v) unsubstituted or substituted C-bonded C.sub.1-C.sub.14-hydrocarbonoxy radical, and the radicals R.sup.7 are in each case independently selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.6-hydrocarbon radical, and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.6-hydrocarbonoxy radical.

23. The mixture M as claimed in claim 22, wherein in formula (II) the radicals R.sup.4, R.sup.5 and R.sup.6 are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C.sub.1-C.sub.6-alkyl radical, (iv) C.sub.1-C.sub.6-alkenyl radical, (v) phenyl radical, and (vi) C.sub.1-C.sub.6-alkoxy radical, and the radical R.sup.7 is selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.6-hydrocarbon radical, and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.6-hydrocarbonoxy radical; and in which in formula (II′) the radicals R.sup.x are each independently selected from the group consisting of (i) hydrogen, (ii) chlorine, (iii) C.sub.1-C.sub.6-alkyl radical, (iv) C.sub.1-C.sub.6-alkenyl radical, (v) phenyl radical, (vi) —O—R.sup.7, and the radicals R.sup.7 are in each case independently selected from the group consisting of (i) unsubstituted or substituted C.sub.1-C.sub.6-hydrocarbon radical, and (ii) unsubstituted or substituted C-bonded C.sub.1-C.sub.6-hydrocarbonoxy radical.

24. The mixture M as claimed in claim 18, wherein in formula (III) the radicals R.sup.y are each independently selected from the group consisting of (i) C.sub.1-C.sub.3-alkyl radical and (ii) triorganosilyl radical of the formula —SiR.sup.b.sub.3, in which the radicals R.sup.b are each independently C.sub.1-C.sub.20-alkyl radicals.

25. The mixture M as claimed in claim 24, wherein in formula (III) the anions X— are selected from the group consisting of the compounds of the formulae [B(R.sup.a).sub.4].sup.− and [Al(R.sup.a).sub.4].sup.−, in which the radicals R.sup.a are in each case independently selected from aromatic C.sub.6-C.sub.14-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 C.sub.1-C.sub.6-alkyl radical, and (iii) triorganosilyl radical of the formula —SiR.sup.b.sub.3, in which the radicals R.sup.b are each independently C.sub.1-C.sub.20-alkyl radicals.

26. The mixture M as claimed in claim 25, wherein in formula (III) all radicals R.sup.y are methyl and the anions X— are selected from the group consisting of the compounds of the formula [B(R.sup.a).sub.4].sup.−, in which the radicals R.sup.a are each independently selected from aromatic C.sub.6-C.sub.14-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 radicals of the formula —SiR.sup.b.sub.3, in which the radicals R.sup.b are each independently C.sub.1-C.sub.20-alkyl radicals.

27. The mixture M as claimed in claim 26, wherein the compound C is selected from the group consisting of Cp*Ge.sup.+B(C.sub.6F.sub.5).sub.4; Cp*Ge.sup.+B[C.sub.6F.sub.4(4-TBS)].sub.4, where TBS=SiMe.sub.2tert-butyl; Cp*Ge.sup.+B(2-NaphF).sub.4, where 2-NaphF=perfluorinated 2-naphthyl radical; and Cp*Ge.sup.+B[(C.sub.6F.sub.5).sub.3(2-NaphF)].sup.−, where 2-NaphF=perfluorinated 2-naphthyl radical.

28. A process for preparing siloxanes by means of a Piers-Rubinsztajn reaction of the mixture M as claimed in claim 18, 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.

29. The process as claimed in claim 28, wherein the temperature is in a range from +40° C. to +200° C. and the pressure is in a range from 0.01 bar to 100 bar.

30. The process as claimed in claim 28, wherein the oxygen originates from an oxygen-containing gas mixture having an oxygen content of 0.1-100% by volume.

31. The process as claimed in claim 30, wherein the reaction is carried out under an air, lean air or oxygen atmosphere.

32. The process as claimed in claim 28, wherein the molar proportion of cationic germanium(II) compound with respect to the Si—H moieties present in the compound A is in a range from 0.001 mol % to 10 mol %.

33. The use of cationic germanium(II) compounds of the general formula (III) as catalyst for Piers-Rubinsztajn reactions.

34. The use as claimed in claim 33, wherein the cationic germanium(II) compound is one of the general formula (IV).

Description

EXAMPLES

[0093] Preparation of Cp*Ge.sup.+B(C.sub.6F.sub.5).sub.4.sup.−

[0094] Under an argon atmosphere, 701 mg (2.04 mmol) of decamethylgermanocene (Cp*.sub.2Ge, Cp*=pentamethylcyclopentadienyl) were dissolved in 5 ml of dichloromethane and a solution of 1.70 g (1.83 mmol) of (C.sub.6H.sub.5).sub.3C.sup.+B(C.sub.6F.sub.5).sub.4.sup.− 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.

[0095] Yield: 1.63 g (97%), pale pink solid.

[0096] .sup.1H-NMR (CD.sub.2Cl.sub.2): δ=2.23 (methyl groups).

[0097] .sup.13C-NMR (CD.sub.2Cl.sub.2): δ=8.82 (methyl groups), δ=123.1 (C's Cp*-Ring), δ=124 (broad), δ=135.3 (m), δ=137.3 (m), δ=139.2 (m), δ=147.2 (m), δ=149.1 (m): aromatic C—F.

[0098] .sup.11B-NMR (CD.sub.2Cl.sub.2): δ=−16.66 (s).

[0099] .sup.19F-NMR (CD.sub.2Cl.sub.2): δ=−167.4 (mc, 8 ortho-F), δ=−163.5 (mc, 4 para-F), δ=−132.9 (m, broad, 8 meta-F).

Example 1

[0100] Oxygen was passed for 3 hours into a solution of 0.30 mg (0.45 μmol) of (π-Me.sub.5C.sub.5)Ge.sup.+B(C.sub.6F.sub.5).sub.4.sup.− in 475 mg of dichloromethane. 178 mg (0.650 mmol) of diethoxydiphenylsilane and 101 mg (0.752 mmol) of 1,1,3,3-tetramethyldisiloxane were then added to this solution, and the mixture was heated to 60° C. for 8 hours. The solvent was then removed under high vacuum. The residue was a colorless, highly viscous oil.

[0101] GPC: M.sub.w=20 700, M.sub.n=6800, M.sub.w/M.sub.n=3.00.

Example 2

[0102] 160 mg (0.587 mmol) of diethoxydiphenylsilane and 101 mg (0.660 mmol) of 1,4-bis(dimethylsilyl)benzene were added to a solution of 0.30 mg (0.45 μmol) of (π-Me.sub.5C.sub.5)Ge.sup.+B(C.sub.6F.sub.5).sub.4.sup.− in 800 mg of dichloromethane, 3×3 ml of air were injected by syringe and the mixture was heated to 70° C. for 4 hours. The solvent was then removed under high vacuum.

[0103] The residue was a colorless, highly viscous oil.

[0104] GPC: M.sub.w=14 600, M.sub.n=5700, M.sub.w/M.sub.n=2.57.

Example 3

[0105] 341 mg (1.25 mmol) of diethoxydiphenylsilane and 361 mg (2.43 mmol) of pentamethyldisiloxane were added to a solution of 0.4 mg (0.5 μmol) of (π-Me.sub.5C.sub.5)Ge.sup.+B(C.sub.6F.sub.5).sub.4.sup.− in 1020 mg of dichloromethane, 3×3 ml of air were injected by syringe and the mixture was heated to 50° C. for 2 hours. The main product of the reaction is 1,1,1,3,3,7,7,9,9,9-decamethyl-5,5-diphenylpentasiloxane. .sup.29Si-NMR (CD.sub.2Cl.sub.2): δ=−48.2 (SiPh.sub.2), −20.2 (2 TMS-SiMe.sub.2), 7.74 (2 Me.sub.3Si). GC-MS: m/z=508 (1%, M.sup.+), 493 (15%, M.sup.+-CH.sub.3).