IP Library Granted Patent US 10,513,584
Granted Patent B2
US 10,513,584 · App. 16/009,366 · Granted Dec 24, 2019

Platinum catalyzed hydrosilylation reactions utilizing cyclodiene additives

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Quick Facts
Patent No.
US 10,513,584
App. No.
16/009,366
Filed
Jun 15, 2018
Granted
Dec 24, 2019
Kind
B2
Art Unit
1622
USPC
556/438
Abstract

A process and composition 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 proviso that when the unsaturated compound is a terminal alkyne, the silyl hydride is other than a halosilane. The process and composition optionally comprise an inhibitor (e). The process and composition may be employed to form a variety of hydrosilylation products.

Claims (20)

1. A composition comprising (a) a silyl hydride, (b) an alkenyl silicone compound, (c) a platinum compound, (d) a cyclodiene, and (e) optionally an inhibitor, where the cyclodiene (d) is 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 saturated or unsaturated ring structure, wherein the ratio of total moles of cyclodiene additive to moles of platinum is less than 2:1.

2. The composition of claim 1 , wherein the diene comprises 1,5-cyclooctadiene; 1,5-dimethyl-1,5-cyclooctadiene; 1,6-dimethyl-1,5-cyclooctadiene, or a combination of two or more thereof.

3. The composition of claim 1 , wherein the ratio of total moles of cyclodiene additive to moles of platinum is from less than 2:1 to about 0.1:1.

4. The composition of claim 1 , wherein the platinum compound is a Pt(0) compound, and the ratio of total moles of cyclodiene additive to moles of platinum is from about 0.1:1 to about 100:1.

5. The composition of claim 1 , wherein the platinum compound is chosen from Karstedt's catalyst, Ashby's catalyst, or a combination thereof.

6. The composition 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.

7. The composition of claim 1 , wherein the alkenyl silicone comprises at least two unsaturated groups and has a viscosity of at least 50 cps at 25° C.

8. The composition of claim 1 , wherein the alkenyl silicone is chosen from an compound of the formula:

M vi a T b D c M d Q e

wherein M vi a =R 31 2 R 32 SiO 1/2 ; T b =R 33 SiO 3/2 where R 33 is chosen from R 31 or R 32 ; D c =R 31 R 33 SiO 2/2 where R 33 is chosen from R 31 or R 32 ; M d =R 31 3 SiO 1/2 ; and Q e =SiO 4/2 ; R 31 is independently selected from a monovalent hydrocarbon radical having one to forty carbon, optionally containing at least one heteroatom; and R 32 is selected from a terminal olefinic monovalent hydrocarbon radical having two to forty carbon atoms, optionally containing at least one heteroatom; wherein the composition of the alkenyl silicone is such as to provide at least two unsaturated groups reactive to hydrosilylation per chain; a≥0, b≥0, d≥0, e≥0; and values for c such that the sum a+b+c+d+e is in the range 50-20,000.

9. The composition of claim 1 , comprising a cure inhibitor (e) chosen from an ethylenically unsaturated amide, an aromatically unsaturated amide, an acetylenic compound, an ethylenically unsaturated isocyanate, an olefinic siloxane, an unsaturated hydrocarbon diester, an unsaturated hydrocarbon mono-ester of an unsaturated acid, an unsaturated anhydride, a conjugated ene-yne, a hydroperoxide, a ketone, a sulfoxide, an amine, a phosphine, a phosphite, a nitrite, a diaziridine, or a combination of two or more thereof.

10. The composition of claim 1 , wherein the concentration of platinum is from about 100 parts per billion (ppb) to about 100 ppm.

11. The composition of claim 1 , wherein component (e) is present in an amount of from about 0 to about 10 weight percent.

12. The composition of claim 1 , wherein components (a)-(e) are provided in a single composition.

13. A coating formed from the composition of claim 12 .

14. A substrate having a surface thereof at least partially coated with the coating of claim 13 .

15. The substrate of claim 14 , wherein the coating is anchored to the surface of the substrate.

16. A cured material prepared from the composition of claim 1 .

17. The cured material of claim 16 , wherein the cured material comprises component (d).

Assignments (10)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (063213/0472) Recorded Oct 22, 2025
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 073168/0715 →
RELEASE OF SECURITY INTEREST Recorded Jul 18, 2025
From: KOOKMIN BANK NEW YORK BRANCH
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 072039/0906 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Mar 31, 2023
From: BNP PARIBAS
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063259/0133 →
FIRST LIEN TERM LOAN PATENT SECURITY AGREEMENT Recorded Mar 31, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 063213/0472 →
RELEASE OF SECURITY INTEREST Recorded Mar 30, 2023
From: KOOKMIN BANK NEW YORK
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063197/0373 →
SECURITY INTEREST Recorded Mar 30, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK NEW YORK BRANCH
Reel/Frame 063197/0475 →
FIRST LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: BNP PARIBAS, AS ADMINISTRATIVE AGENT
Reel/Frame 049387/0782 →
SECOND LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK, NEW YORK BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 049388/0220 →
ABL PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.; MOMENTIVE PERFORMANCE MATERIALS GMBH
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 049388/0252 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2018
From: ROY, AROOP K.; BOYER, JULIE L.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 046097/0381 →