Granted Patent B2

US 9,434,749 · App. 14/737,930 · Granted Sep 6, 2016

Abstract

Claims (28)

1. A process for the hydrosilylation of an unsaturated compound comprising reacting (a) a silyl hydride with (b) an unsaturated compound in the presence of (c) a platinum compound and (d) a cyclodiene, with the provisos that (i) when the unsaturated compound is a terminal alkyne, the silyl hydride is other than a halosilane, and (ii) when the platinum compound is a Pt(II)-based compound, the ratio of total moles of cyclodiene to moles of platinum is less than 3:1.

2. The process of claim 1 , wherein the cyclodiene is chosen from a compound of the formula:

wherein R 1 -R 8 , R 3′ , R 4′ , R 7′ , and R 8′ are independently hydrogen; an substituted or unsubstituted alkyl or aryl group optionally containing at least one heteroatom; an alkoxy; and a halogen radical; optionally R 1 -R 2 and/or R 5 -R 6 taken together may form a ring structure.

3. The process of claim 1 , wherein the cyclodiene comprises 1,5-cyclooctadiene; 1,5-dimethyl-1,5-cyclooctadiene; 1,6-dimethyl-1,5-cyclooctadiene, or a combination of two or more thereof.

4. The process of claim 1 , wherein the platinum compound is a Pt(II)-based compound, and the ratio of total moles of cyclodiene additive to moles of platinum is less than 2:1.

5. The process of claim 1 , wherein the platinum compound is a Pt(II)-based compound, and the ratio of total moles of cyclodiene additive to moles of platinum is about 1:1 or lower.

6. The process of claim 1 , wherein the platinum compound is a Pt(II)-based compound, and the ratio of total moles of cyclodiene additive to moles of platinum is from about 0.1:1 to about 2:1.

7. The process of claim 1 , wherein the unsaturated compound is chosen from an unsaturated polyether; an alkyl capped allyl polyether; a methylallyl polyether; a terminally unsaturated amine; an alkyne; a C2-C45 linear or branched olefin; an unsaturated epoxide; a terminally unsaturated acrylate; a terminally unsaturated methacrylate; a terminally unsaturated diene; an aliphatically unsaturated aryl ether; an aliphatically unsaturated aromatic hydrocarbon; an unsaturated cycloalkane; a vinyl-functionalized polymer or oligomer; a vinyl-functionalized and/or terminally unsaturated allyl-functionalized or alkenyl-functionalized silane or siloxane; an unsaturated fatty acid; an unsaturated fatty ester; an aliphatically unsaturated synthetic or natural mineral; or a combination of two or more thereof.

8. The process of claim 1 , wherein the unsaturated compound is chosen from polyoxyalkylenes having the general formula:

R 25 (OCH 2 CH 2 ) z (OCH 2 CHR 27 ) w —OR 26 ;

R 26 O(CHR 27 CH 2 O) w (CH 2 CH 2 O) z —CR 28 2 —C≡C—CR 28 2 (OCH 2 CH 2 ) z (OCH 2 CHR 27 ) w OR 26

H 2 C═CR 28 CH 2 O(CH 2 CH 2 O) z (CH 2 CHR 27 O) w CH 2 CR 28 ═CH 2

wherein R 25 is independently an unsaturated organic group containing from 2 to 10 carbon atoms; R 26 is independently hydrogen, an acyl group, or an alkyl group having from 1 to 8 carbon atoms; R 27 is independently a monovalent hydrocarbon group; R 28 independently chosen from hydrogen and a monovalent hydrocarbon group; each occurrence of z is 0 to 100 inclusive; and each occurrence of w is 0 to 100 inclusive.

9. The process of claim 1 , wherein the silylhydride is chosen from a compound of the formula R 9 m SiH p X 4-(m+p) and/or M a M H b D c D H d T e T H f Q g , where each R 9 is independently a substituted or unsubstituted aliphatic or aromatic hydrocarbyl group, X is alkoxy, acyloxy, halogen, or silazane, m is 1-3, p is 1-3 the subscripts a, b, c, d, e, f, and g are such that the molar mass of the silylhydride is between 100 and 100,000 Dalton; M represents a monofunctional group of formula R 10 3 SiO 1/2 , a D represents a difunctional group of formula R 11 2 SiO 2/2 , a T represents a trifunctional group of formula R 12 SiO 3/2 , Q represents a tetrafunctional group of formula SiO 4/2 , M H represents HR 13 2 SiO 1/2 , T H represents HSiO 3/2 , and D H represents R 14 HSiO 2/2 ; each occurrence of R 10-14 is independently C1-C18 alkyl, C1-C18 substituted alkyl, C6-C14 aryl or substituted aryl, wherein R10-14 optionally contains at least one heteroatom.

10. The process according to claim 1 , wherein the silylhydride is a chlorosilane.

11. The process of claim 1 , wherein the silylhydride is a compound of the formula R 15 R 16 R 17 Si(CH 2 R 18 ) x SiOSiR 19 R 20 (OSiR 21 R 22 ) y OSiR 23 R 24 H, where R 15 -R 24 are independently chosen from hydrogen, a monovalent alkyl group, a cycloalkyl group, and an aryl group; x has a value of 1-8, and y has a value from zero to 10.

12. The process of claim 11 , wherein the ratio of cyclodiene to platinum is about 1:1.

13. The process of claim 1 , wherein the platinum compound is chosen from platinum halides, platinum siloxane complexes, cycloalkadiene-platinum complexes, or a combination of two or more thereof.

14. The process of claim 1 , wherein the platinum compound is chloroplatinic acid.

15. The process of claim 1 , wherein the platinum compound is a Pt(0)-based compound.

16. The process of claim 15 , wherein the platinum compound is chosen from a vinylsiloxane-complexed Pt catalyst.

17. The process of claim 15 where the ratio of cyclodiene to Pt(0) is 0.1:1 to 100:1.

18. The process according to claim 1 where the unsaturated compound is allyl methacrylate.

19. The process of claim 1 , wherein the unsaturated compound is allyl glycidyl ether.

20. The process of claim 1 where the unsaturated compound is an allyl or methallyl polyether.

21. The process of claim 1 where the reaction is carried out at a temperature of −50° C. to 250° C.

22. The process of claim 1 where the reaction is conducted in the presence of a solvent chosen from a hydrocarbon, a halogenated hydrocarbon, an ether, an alcohol, or a combination of two or more thereof.

23. The process of claim 1 , wherein the platinum concentration is from about 100 parts per billion to about 100 parts per million.

Assignments (10)