Composition of olefinically functionalised siloxane oligomers based on alkoxy silanes

1. A composition, comprising an olefinically functionalized siloxane oligomer having not more than one olefinic radical on a silicon atom thereof, wherein

the olefinically functionalized siloxane oligomer has a Si—O-crosslinked structural element which forms catenary, cyclic, crosslinked or optionally three-dimensionally crosslinked structures, with a structure of formula I,

(R 1 O)[(R 1 O) 1-x (R 2 ) x Si(A)O] a [Si(Y) 2 O] c [Si(B)(R 4 ) y (OR 3 ) 1-y O] b R 3   (I),

the structural elements are derived from alkoxysilanes,

wherein A is an olefinic radical selected from a linear, branched or cyclic alkenyl- or cycloalkenyl-alkylene-functional group having in each case 2 to 16 C atoms, and

B is a saturated hydrocarbon radical selected from a linear, branched or cyclic alkyl radical having 1 to 16 C atoms,

Y is OR 3 or, in crosslinked and optionally three-dimensionally crosslinked structures, independently at each occurrence, OR 3 or O 1/2 , where

R 1 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 4 C atoms or H,

R 2 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 15 C atoms,

R 3 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 4 C atoms or H, and

R 4 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 15 C atoms,

a, b, c, x and y are each independently an integer, wherein 1≦a, 0≦b, 0≦c, x independently at each occurrence is 0 or 1, y independently at each occurrence is 0 or 1, and (a+b+c)≧2,

the structural elements [(R 1 O) 1-x (R 2 ) x Si(A)O] a , [Si(B)(R 4 ) y (OR 3 ) 1-y O] b and [Si(Y) 2 O] c , in relation to all silicon atoms of formula I, are present at less than or equal to 80% and greater than or equal to 30% as M structure,

a weight-average molecular weight (Mw) is greater than or equal to 315 g/mol, and

an amount of residues of the acid catalyst during preparation is less than or equal to 250 mg/kg of composition,

wherein

a weight-average molecular weight (Mw) is greater than 315 g/mol

a number-average molecular weight (Mn) is greater than 300 g/mol, and a polydispersity (D), as a ratio of Mw/Mn, is from 1.05 to 1.25.

2. The composition according to claim 1 ,

wherein

the siloxane oligomer has derived structural elements from at least one alkoxysilane selected from:

(i) olefinically functionalized alkoxysilanes of formula II,

A-Si(R2) x (OR1)3 −x   (II)

wherein A is an olefinic radical selected from a linear, branched or cyclic alkenyl- or cycloalkenyl-alkylene-functional group having in each case 2 to 16 C atoms, where R 2 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 15 C atoms and x is 0 or 1, and R 1 independently at each occurrence is a methyl, ethyl or propyl group, and optionally

(ii) alkoxysilane of formula III, functionalized with a saturated hydrocarbon radical,

B—Si(R 4 ) y (OR 3 ) 3-y   (III)

wherein B is an unsubstituted hydrocarbon radical selected from a linear, branched or cyclic alkyl radical having 1 to 16 C atoms,

where R 4 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 15 C atoms and y is 0 or 1, and R 3 independently at each occurrence is a methyl, ethyl or propyl group, and optionally

(iii) a tetraalkoxysilane of formula IV which is Si(OR 3 ) 4 , wherein R 3 independently at each occurrence is as defined above.

3. The composition according to claim 2 ,

wherein

in the olefinically functionalized alkoxysilanes of formula II, x is 0, and optionally in the alkoxysilane of formula III functionalized with a saturated hydrocarbon radical, y is 0.

4. The composition according to claim 3 ,

wherein

the amount of residues of the acid catalyst in the preparation, in terms of chlorine, chloride or total chloride, is less than or equal to 250 mg/kg of the composition.

5. The composition according to claim 1 ,

wherein,

selected in each case independently of one another

(i) the structural element [(R 1 O) 1-x (R 2 ) x Si(A)O] a in formula I is present, in relation to all silicon atoms of formula I, at 0.0% to 8.0% as T structure,

(ii) the structural elements [(R 1 O) 1-x (R 2 ) x Si(A)O] a and [Si(B)(R 4 ) y (OR 3 ) 1-y O] b and [Si(Y) 2 O] c in formula I are present together, in relation to all silicon atoms of formula I, at less than or equal to 75% to 40% as D structure,

(iii) the structural element [(R 1 O) 1-x (R 2 ) x Si(A)O] a in formula I is present, in relation to all silicon atoms of formula I, at 25% to 55% as M structure,

(iv) the structural element [Si(B)(R 4 ) y (OR 3 ) 1-y O] b in formula I, is present, in relation to all silicon atoms of formula I, at less than or equal to 40% as M structure,

(v) the structural element [Si(Y) 2 O] c in formula I is present at greater than 20% as D structure, and

(vi) the structural element [Si(Y) 2 O] e in formula I is present at 0.0% to 1% as T structure.

6. The composition according to claim 1 ,

wherein

a weight-average molecular weight (Mw) is from greater than or equal to 350 g/mol to 800 g/mol.

7. The composition according to claim 6 ,

wherein

the weight-average molecular weight (Mw) is from greater than or equal to 350 g/mol to 750 g/mol.

8. The composition according to claim 2 ,

wherein

in formulae I, II, or both, the olefinic radical A, independently at each occurrence, is selected from a vinyl, allyl, butenyl, 3-butenyl, pentenyl, hexenyl, ethylhexenyl, heptenyl, octenyl, cyclohexenyl-C1 to C8-alkylene-cyclohexenyl-2-ethylene, 3′-cyclohexenyl-2-ethylene, cyclohexadienyl-C1 to C8-alkylene or cyclohexadienyl-2-ethylene group, and independently thereof

in formulae I, III, or both, the unsubstituted hydrocarbon radical B, independently at each occurrence, is selected from a methyl, ethyl, propyl, isobutyl, octyl or hexadecyl group, and independently at each occurrence, R 1 is a methyl, ethyl or propyl group and R 3 independently is a methyl, ethyl or propyl group.

9. The composition according to claim 2 ,

wherein

in formulae I, II, or both, the olefinic radical A is a vinyl group, and independently thereof

in formulae I, III, or both, the unsubstituted hydrocarbon radical B is selected from a methyl, ethyl, propyl, butyl, isobutyl, n-butyl, tert-butyl, pentyl, n-pentyl, isopentyl, neopentyl, hexyl, isohexyl, neohexyl, heptyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 2-methylpentyl, 3-methylpentyl, octyl, n-octyl, isooctyl, nonyl, decyl, undecyl, dodecyl, C 13 H 27 —, C 14 H 29 —, C 15 H 31 — and hexadecyl group, and

independently at each occurrence, R 1 is a methyl, ethyl or propyl group and R 3 independently is a methyl, ethyl or propyl group.

10. The composition according to claim 1 ,

wherein the olefinically functionalized siloxane oligomer is present at greater than or equal to 90% (area %) in relation to the overall composition, with a molecular weight of less than or equal to 1000 g/mol in the composition.

11. The composition according to claim 1 ,

wherein

c in formula I is 0.

12. The composition according to claim 1 ,

wherein

a weight-average molecular weight (Mw) is greater than or equal to 420 g/mol, a number-average molecular weight (Mn) is greater than or equal to 400 g/mol, and a polydispersity (D), as a ratio of Mw/Mn, is from 1.05 to 1.25.

13. The composition according to claim 1 ,

wherein

a weight-average molecular weight (Mw) is greater than 450 g/mol to 590 g/mol, a number-average molecular weight (Mn) is greater than 410 g/mol to 510 g/mol, and a polydispersity (D), as a ratio of Mw/Mn, is from 1.05 to 1.25.

14. The composition according to claim 1 ,

wherein

the olefinically functionalized siloxane oligomer is present at greater than or equal to 45% (area %, GPC) as trisiloxane, tetrasiloxane, cyclotetrasiloxane and/or cyclopentasiloxane in the composition.

15. The composition according to claim 1 ,

wherein

the composition suffers a loss of mass of 50 wt %, determined by thermogravimetric analysis, at a temperature above 210° C.

16. The composition according to claim 15 ,

wherein

the loss of mass by the composition as determined by TGA (platinum crucible, lid with hole, 10 K/min) at a temperature up to and including 140° C. is less than 5 wt %.

17. The composition according to claim 1 ,

wherein

a ratio of M to D structures in the siloxane oligomer or in formula I, in relation to all silicon atoms, is from 1:2 to 10:1.

18. The composition according to claim 2 ,

wherein

a) the siloxane oligomer and a structure of formula I, in each case derived from alkoxysilanes of formula II as olefinic radical A, have a vinyl group, where R 1 independently at each occurrence is a methyl or ethyl group,

b) the siloxane oligomer and a structure of formula I, in each case derived from alkoxysilanes of formula II as olefinic radical A, have a vinyl group and, derived from alkoxysilanes of formula III as unsubstituted hydrocarbon radical B, have a propyl group, where R 1 and R 3 independently at each occurrence is a methyl or ethyl group, or

c) the siloxane oligomer and a structure of formula I, in each case derived from alkoxysilanes of formula II and formula IV and optionally of formula III, are selected from a) or b), where R 3 , derived from formula IV, independently at each occurrence is a methyl or ethyl group.

19. The composition according to claim 2 ,

wherein

in each case independently, the siloxane oligomer is derived from an olefinically functionalized alkoxysilane of general formula II which is selected from vinyltriethoxysilane and vinyltrimethoxysilane, and optionally from an alkoxysilane of formula III, the alkoxysilane of the formula III, independently at each occurrence, being selected from the group consisting of methyltriethoxysilane, methyltrimethoxysilane, ethyltriethoxysilane, ethyltrimethoxysilane, propyltriethoxysilane, propyltrimethoxysilane, butyltriethoxysilane, butyltrimethoxysilane, n-butyltriethoxysilane, n-butyltrimethoxysilane, isobutyltriethoxysilane, isobutyltrimethoxysilane, hexyltriethoxysilane, hexyltrimethoxysilane, n-hexyltriethoxysilane, n-hexyltrimethoxysilane, isohexyltriethoxysilane, isohexyltrimethoxysilane, octyltriethoxysilane, octyltrimethoxysilane, n-octyltriethoxysilane, n-octyltrimethoxysilane, isooctyltriethoxysilane, isooctyltrimethoxysilane, undecyltriethoxysilane, undecyltrimethoxysilane, decyltriethoxysilane, decyltrimethoxysilane, nonadecyltriethoxysilane, nonadecyltrimethoxysilane, dodecyltriethoxysilane, dodecyltrimethoxysilane, C 13 H 27 -triethoxysilane, C 13 H 27 -trimethoxysilane, C 14 H 29 -triethoxysilane, C 14 H 29 -trimethoxysilane, C 15 H 31 -trimethoxysilane, C 15 H 31 -triethoxysilane, hexadecyltriethoxysilane and hexadecyltrimethoxysilane, and a transesterification product thereof.

20. A process for preparing a composition according to claim 1 , comprising olefinically functionalized siloxane oligomers, the process comprising reacting at least

an olefinically functionalized alkoxysilane of formula II,

A-Si(R 2 ) x (OR 1 ) 3-x   (II),

where in formula II A is an olefinic radical selected from a linear, branched or cyclic alkenyl- or cycloalkenyl-alkylene-functional group having in each case 2 to 16 C atoms, R 2 is independently a linear, branched or cyclic alkyl radical having 1 to 15 C atoms and x is 0 or 1 and R 1 is independently a linear, branched or cyclic alkyl radical having 1 to 4 C atoms,

in the presence of an acidic hydrolysis catalyst, condensation catalyst, or both,

with water in a defined molar ratio of water to alkoxysilane alkoxy groups of from 1:2.75 to 1:5.0, in the presence of a solvent, to obtain the siloxane oligomer;

separating off the hydrolysis alcohol and the solvent present substantially; and

obtaining the composition comprising olefinically functionalized siloxane oligomer as a liquid-phase product.

21. The process according to claim 20 ,

wherein an olefinically functionalized alkoxysilane of general formula II is reacted in the presence of an acidic hydrolysis catalyst, condensation catalyst, or both, with

an alkoxysilane of formula III,

B—Si(R 4 ) y (OR 3 ) 3-y   (III),

wherein B is a saturated hydrocarbon radical selected from a linear, branched or cyclic alkyl radical having 1 to 16 C atoms, R 3 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 4 C atoms, R 4 is a linear, branched or cyclic alkyl radical having 1 to 15 C atoms, and y is 0 or 1.

22. The process according to claim 21 ,

wherein an olefinically functionalized alkoxysilane of general formula II, and optionally an alkoxysilane of formula III, are reacted in the presence of an acidic hydrolysis catalyst, a condensation catalyst, or both, with

a tetraalkoxysilane of formula IV,

Si(OR 3 ) 4   (IV),

wherein R 3 independently at each occurrence is a linear, branched or cyclic alkyl radical having 1 to 4 C atoms.

23. The process according to claim 20 ,

wherein

the reaction takes place in the presence of an alcohol as solvent.

24. The process according to claim 21 , wherein the alkoxysilane of formula II and optionally the alkoxysilane of formula III are reacted with water in a defined molar ratio of water to alkoxysilane alkoxy groups of from 1:3 to 1:4.5 to obtain siloxane oligomers.

25. The process according to claim 21 ,

wherein

in the olefinically functionalized alkoxysilane of formula II,

A-Si(R 2 ) x (OR 1 ) 3-x   (II),

A is selected from a vinyl, allyl, butenyl, pentenyl, hexenyl, ethylhexenyl, heptenyl, octenyl, cyclohexenyl-C1 to C8-alkylene, cyclohexenyl-2-ethylene, 3′-cyclohexenyl-2-ethylene and cyclohexadienyl-C1 to C8-alkylene group, and R 1 independently is a methyl, ethyl or propyl group and x is 0 or 1, and independently

in the alkoxysilane of formula III,

B—Si(R 4 ) y (OR 3 ) 3-y   (III),

the unsubstituted hydrocarbon radical B is selected from a methyl, ethyl, propyl, butyl, isobutyl, octyl, butyl, n-butyl, tert-butyl, pentyl, n-pentyl, isopentyl, neopentyl, hexyl, isohexyl, neohexyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 2-methylpentyl, 3-methylpentyl, heptyl, n-heptyl, octyl, isooctyl, nonyl, decyl, undecyl, dodecyl, C 13 H 27 , C 14 H 29 , C 15 H 31 and hexadecyl group, and R 3 is a methyl, ethyl or propyl group and y is 0 or 1.

26. The process according to claim 21 ,

wherein

in the olefinically functionalized alkoxysilane of formula II, x is 0, and/or in the alkoxysilane of formula III functionalized with a saturated hydrocarbon radical, y is 0.

27. The process according to claim 26 ,

wherein

in each case independently

the olefinically functionalized alkoxysilane of the general formula II is selected from the group consisting of vinyltriethoxysilane, allyltriethoxysilane, butenyltriethoxysilane, pentenyltriethoxysilane, hexenyltriethoxysilane, ethylhexenyltriethoxysilane, heptenyltriethoxysilane, octenyltriethoxysilane, cyclohexenyl-C1 to C8-alkylenetriethoxysilane, cyclohexenyl-2-ethylenetriethoxysilane, 3′-cyclohexenyl-2-ethylenetriethoxysilane, cyclohexadienyl-C1 to C8-alkylenetriethoxysilane or cyclohexadienyl-2-ethylenetriethoxysilane, vinyltrimethoxysilane, allyltrimethoxysilane, butenyltrimethoxysilane, pentenyltrimethoxysilane, hexenyltrimethoxysilane, ethylhexenyltrimethoxysilane, heptenyltrimethoxysilane, octenyltrimethoxysilane, cyclohexenyl-C1 to C8-alkylenetrimethoxysilane, cyclohexenyl-2-ethylenetrimethoxysilane, 3′-cyclohexenyl-2-ethylenetrimethoxysilane, cyclohexadienyl-C1 to C8-alkylenetrimethoxysilane and cyclohexadienyl-2-ethylenetrimethoxysilane, and in each case independently

the alkoxysilane of formula III is selected from the group consisting of methyltriethoxysilane, ethyltriethoxysilane, n-propyltriethoxysilane, isopropyltriethoxysilane, butyltriethoxysilane, n-butyltriethoxysilane, isobutyltriethoxysilane, hexyltriethoxysilane, n-hexyltriethoxysilane, isohexyltriethoxysilane, heptyltriethoxysilane, octyltriethoxysilane, n-octyltriethoxysilane, isooctyltriethoxysilane, undecyltriethoxysilane, decyltriethoxysilane, nonadecyltriethoxysilane, dodecyltriethoxysilane, C 13 H 27 -triethoxysilane, C 14 H 29 -triethoxysilane or C 15 H 31 -triethoxysilane, hexadecyltriethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, n-propyltrimethoxysilane, isopropyltrimethoxysilane, butyltrimethoxysilane, n-butyltrimethoxysilane, isobutyltrimethoxysilane, hexyltrimethoxysilane, n-hexyltrimethoxysilane, isohexyltrimethoxysilane, heptyltrimethoxysilane, octyltrimethoxysilane, n-octyltrimethoxysilane, isooctyltrimethoxysilane, undecyltrimethoxysilane, decyltrimethoxysilane, nonadecyltrimethoxysilane, dodecyltrimethoxysilane, C 13 H 27 -trimethoxysilane, C 14 H 29 -trimethoxysilane or C 15 H 31 -trimethoxysilane and hexadecyltrimethoxysilane, and in each case independently

the alkoxysilane of formula IV is selected from the group consisting of tetraethoxysilane and tetramethoxysilane.

28. The process according to claim 20 ,

wherein

a vinyltrimethoxysilane or a vinyltriethoxysilane is reacted.

29. The process according to claim 22 ,

wherein

the alkoxysilanes of at least one of formulae II, III and IV are subjected to at least partial hydrolysis and condensation in the presence of the acidic hydrogen chloride catalyst.

30. The process according to claim 20 ,

wherein

a total chloride content of less than or equal to 250 mg/kg is set.

31. The process according to claim 20 ,

wherein

a total number of silicon atoms in the siloxane oligomer are present at less than or equal to 80% to greater than or equal to 35% as M structure, for a weight-average molecular weight (Mw) of greater than or equal to 315 g/mol.

32. The process according to claim 22 ,

wherein

vinyltrimethoxysilane is the alkoxysilane of formula II,

vinyltriethoxysilane is the alkoxysilane of formula II,

as alkoxysilanes of formulae II and III, vinyltrimethoxysilane and propyltrimethoxysilane, vinyltriethoxysilane and propyltriethoxysilane, vinyltriethoxysilane and propyltrimethoxysilane or vinyltrimethoxysilane and propyltriethoxysilane are used, or in a), b) or c) the alkoxysilanes with corresponding mixed methoxy- and ethoxy-functionalization are used

or

d) additionally in a), b) or c), as alkoxysilane of formula IV, a tetraethoxysilane, tetramethoxysilane or a mixture thereof is used.

33. The process according to claim 22 , comprising:

initially introducing an (i) olefinically functionalized alkoxysilane of formula II or an olefinic functionalized alkoxysilane of formula I and an alkoxysilane of formula III and in each case optionally an alkoxysilane of formula IV; and then

adding a mixture comprising solvent, water, and HCl as acidic hydrolysis catalyst, condensation catalyst, or both, the solvent being the alcohol corresponding to the hydrolysis alcohol, and setting a defined molar ratio of water to alkoxysilane alkoxy groups of from 1:2.75 to 5.0, with the alcohol in an amount by weight of from 0.2 to 8 times in relation to a weight of the alkoxysilanes of formulae II, III and optionally IV.

34. The process according to claim 33 , wherein the alcohol is present in an amount by weight of from 0.2 to 1.5 times in relation to the weight of the silanes of formulae II, III and optionally IV.