IP Library Granted Patent US 7,786,200
Granted Patent B2
US 7,786,200 · App. 12/221,175 · Granted Aug 31, 2010

Sulfur-containing silane, filled elastomeric compositions containing same and articles made therefrom

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Quick Facts
Patent No.
US 7,786,200
App. No.
12/221,175
Granted
Aug 31, 2010
Kind
B2
Abstract

Sulfur-containing silane and its partially to substantially complete hydrolyzate(s) are useful as additives for filled elastomeric compositions for tires and other cured rubber articles.

Claims (62)

1. A sulfur-containing silane of general Formula (1):

[Y 1 SG 1 SiZ θ ] m [Y 2 SG 2 SiZ θ Z β ] n [Y 3 SG 3 SiZ β 3 ] o [Y 4 SG 4 SiZ β 2 X] p [Y 5 SG 5 SiZ β X 2 ] q [X] r   (1)

wherein:

each occurrence of G 1 , G 2 , G 3 , G 4 and G 5 is independently a hydrocarbylene group containing up to 15 carbon atoms selected from the group consisting of alkylene, alkenylene, arylene, and aralkylene groups;

each occurrence of X is independently selected from the group consisting of —R, —OR, —OC(═O)R 3 , H-A 2 G 6 (OH)(O—), R 1 A 1 C(═O)A 2 G 6 (OH)O— and [R 1 A 1 C(═O)A 2 ] 2 G 6 O—, wherein each occurrence of A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group, an oxygen atom and —NR 2 —; each occurrence of A 2 is independently selected from a covalent chemical bond between G 6 and the carbonyl group, an oxygen atom and —NR 2 —; each occurrence of R is independently selected from the group consisting of straight, cyclic and branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 12 carbon atoms; each occurrence of R 1 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; each occurrence of R 2 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; each occurrence of R 3 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl groups, alkenyl groups, aryl groups, and aralkyl groups containing from 1 to 29 carbon atoms; and G 6 is independently a hydrocarbylene group of from 3 to 15 carbon atoms;

each occurrence of Y 1 , Y 2 , Y 3 , Y 4 , and Y 5 is independently selected from hydrogen and an acyl group, R 3 C(═O)—, wherein each occurrence of R 3 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 30 carbon atoms;

each occurrence of Z β , which forms a bridging structure between two silicon atoms, is selected from the group consisting of [R 1 A 1 C(═O)A 2 G 6 (O—) 2 ] 0.5 and [H-A 2 G 6 (O—) 2 ] 0.5 , wherein each occurrence of A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group, an oxygen atom and —NR 2 ; each occurrence of A 2 is independently selected from the group consisting of a covalent chemical bond between G 6 and the carbonyl group, oxygen atom and —NR 2 —; each occurrence of R 1 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; each R 2 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; and each occurrence of G 6 is independently a hydrocarbylene group of from 3 to 15 carbon atoms;

each occurrence of Z θ , which forms a cyclic structure with a silicon atom, is independently selected from the group consisting of R 1 A 1 C(═O)A 2 G 6 (O—) 2 and H-A 2 G 6 (O—) 2 , wherein each occurrence of A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group, oxygen atom and —NR 2 —; each occurrence of A 2 is independently selected from the group consisting of a covalent chemical bond between G 6 and the carbonyl group, oxygen atom and —NR 2 —; each occurrence of R 1 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl groups, alkenyl groups, aryl groups, and aralkyl groups containing from 1 to 18 carbon atoms; each occurrence of R 2 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl groups, alkenyl groups, aryl groups, and aralkyl groups containing from 1 to 18 carbon atoms; and each occurrence of G 6 is independently a hydrocarbylene group of from 3 to 15 carbon atoms;

each occurrence of subscripts m, n, o, p, q and r independently is an integer wherein m is 0 or 1; n is 0 to 18; o is 0 to 20; and, p is 0 to 20; q is 0 to 20 and r is 0 or 1, with the provisos that,

(i) when m is 1, r is 1 and n+o+p+q is 0,

(ii) when m is 0, r is 0 and n+o+p+q is equal to or greater than 2, and

(iii) the silane contain at least one Z β with the structure [R 1 A 1 C(═O)A 2 G 6 (O—) 2 ] 0.5 or at least one Z θ of the structure R 1 A 1 C(═O)A 2 G 6 (O—) 2 .

2. The sulfur-containing silane of claim 1 wherein:

each occurrence of G 1 , G 2 , G 3 , G 4 and G 5 is independently a hydrocarbylene group containing a straight or branched chain alkylene group of from 1 to 6 carbon atoms; each occurrence of X is independently selected from the group consisting of —R, [R 1 A 1 C(═O)A 2 ] 2 G 6 O— and R 1 A 1 C(═O)A 2 G 6 (OH)O—, wherein each A 1 is a covalent bond between R 1 and the carbonyl group; each A 2 is an oxygen atom; each R is independently a straight chain alkyl group containing from 1 to 6 carbon atoms; each R 1 is independently an alkyl group containing from 2 to 12 carbon atoms; each R 2 is independently selected from the group consisting of hydrogen and an alkyl group containing from 1 to 6 carbon atoms; and G 6 is independently a trivalent alkylene group of from 3 to 6 carbon atoms considered as derived from an alkane;

each occurrence of Y 1 , Y 2 , Y 3 , Y 4 , and Y 5 is selected from hydrogen and an acyl group, R 3 C(═O)—, wherein R 3 is an alkyl group of from 6 to 12 carbon atoms;

each occurrence of Z β , which forms a bridging structure between two silicon atoms, is independently [R 1 A 1 C(═O)A 2 G 6 (O—) 2 ] 0.5 , wherein each A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group; each A 2 is an oxygen atom; each R 1 is independently an alkyl group containing from 2 to 12 carbon atoms; and each G 6 is independently a trivalent alkylene group of from 3 to 6 carbon atoms considered as derived from an alkane; and,

each occurrence of Z θ , which forms a cyclic structure with a silicon atom, is independently R 1 A 1 C(═O)A 2 G 6 (O—) 2 , wherein each A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group; each A 2 is an oxygen atom; each R 1 is independently an alkyl group containing from 2 to 12 carbon atoms; and G 6 is independently a trivalent alkylene group of from 3 to 6 carbon atoms derived from an alkane.

3. The sulfur-containing silane of claim 2 wherein m is 1, r is 1 and n+o+p+q is 0.

4. The sulfur-containing silane of claim 3 wherein m is 0, r is 0 and n+o+p+q is equal to or greater than 2.

5. The sulfur-containing silane of claim 1 wherein X is [R 1 A 1 C(═O)A 2 ] 2 G 6 O— and R 1 A 1 C(═O)A 2 G 6 (OH)O—, wherein each A 1 is a covalent bond between R 1 and the carbonyl group; each A 2 is an oxygen atom; each R is independently a straight chain alkyl group containing from 1 to 6 carbon atoms; each R 1 is independently an alkyl group containing from 2 to 12 carbon atoms; each R 2 is independently selected from the group consisting of a hydrogen and an alkyl group containing from 1 to 6 carbon atoms; and G 6 is independently a trivalent alkylene group of from 3 to 6 carbon atoms derived from an alkane.

6. The sulfur containing silane of claim 5 wherein R 1 is octyl and G 6 is CH 3 CH 2 C(CH 2 —) 3 .

7. The sulfur-containing silane of claim 1 wherein Y 1 , Y 2 , Y 3 , Y 4 and Y 5 are hydrogen.

8. The sulfur-containing silane of claim 1 which is at least one silane selected from the group consisting of hexanoic acid 2-(3-butyrylsulfanyl-propyl)-5-ethyl-2-methyl-[1,3,2]dioxasilinan-5-yl ester, hexanoic acid 2-(3-butyrylsulfanyl-propyl)-5-ethyl-2-ethoxy-[1,3,2]dioxasilinan-5-yl ester, hexanoic acid 2-(3-butyrylsulfanyl-propyl)-2-(3-hexanoyloxy-4-hydroxy-propoxy)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(3-hexanoyloxymethyl-4-hydroxy-3-methyl-propoxy)-2-(3-hexanoylsulfanyl-propyl)-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 2-(3-hexanoyloxymethyl-4-hydroxy-3-methyl-propoxy)-2-(3-mercapto-propyl)-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, 2-ethyl-hexanoic acid 2-[3-(2-ethyl-hexanoyloxymethyl)-4-hydroxy-3-methyl-propoxy]-2-[3-(2-ethyl-hexanoylsulfanyl)-propyl]-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, 2-ethyl-hexanoic acid 2-[4-(2-ethyl-hexanoyloxy)-3-methyl-butoxy]-2-[3-(2-ethyl-hexanoylsulfanyl)-propyl]-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 5-ethyl-2-(3-mercapto-propyl)-2-methyl-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-ethoxy-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester,octanoic acid 2-(2,2-bis-hydroxymethyl-butoxy)-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-(2-hydroxymethyl-2-octanoyloxymethyl-butoxy)-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(2,2-bis-octanoyloxymethyl-butoxy)-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(2,2-bis-octanoyloxymethyl-butoxy)-5-ethyl-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-(2-hydroxymethyl-2-octanoyloxymethyl-butoxy)-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-{2-[5-ethyl-5-hydroxymethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-2-yloxymethyl]-2-octanoyloxymethyl-butoxy}-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-{2-[5-ethyl-5-octanoyloxymethyl-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxymethyl]-2-octanoyloxymethyl-butoxy}-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, Octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-(3-ethyl-3-methyl-heptanoylamino)-2-(octanoylamino-methyl)-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-octanoylamino-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexyloxycarbonyloxy-2-hexyloxycarbonyloxymethyl-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexyloxycarbonyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexylcarbamoyloxy-2-hexylcarbamoyloxymethyl-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexylcarbamoyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexylcarbamoyloxy-2-hexylcarbamoyloxymethyl-3-[2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexylcarbamoyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, acetic acid 2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, N-{2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl}-acetamide, carbonic acid 2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester propyl ester, thioacetic acid S-[3-(ethoxy-{2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-propoxycarbonyloxymethyl-butoxy}-methyl-silanyl)-propyl]ester, thioacetic acid S-[3-(ethoxy-{2-[ethoxy-(4-mercapto-butyl)-ethoxy-silanyloxymethyl]-2-propoxycarbonyloxymethyl-butoxy}-ethoxy-silanyl)-propyl]ester, acetic acid 2-{2-acetoxymethyl-2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-methyl-silanyloxymethyl]-butoxy}-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 2-{2-octanoyloxymethyl-2-[{2-octanoyloxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-octanonylsulfanyl-propyl)-methyl-silanyloxymethyl]-butoxy}-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-ylmethyl ester, acetic acid 2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-ethoxy-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, acetic acid 2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-methyl-silanyloxymethyl]-2-[(3-acetylsulfanyl-propyl)-ethoxy-methyl-silanyloxymethyl]-butyl ester, octanoic acid 2-[{2-octanoyloxymethyl-2-[ethoxy-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butoxy}-(3-octanoylsulfanyl-propyl)-methyl-silanyloxymethyl]-2-[(3-octanoylsulfanyl-propyl)-diethoxy-silanyloxymethyl]-butyl ester, acetic acid 2,2-bis-[(3-acetylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-methyl-silanyloxymethyl]-butyl ester, acetic acid 2,2-bis-[(3-acetylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-ethoxy-silanyloxymethyl]-butyl ester, octanoic acid 2-[(3-octanoylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-ethyl-silanyloxymethyl]-2-[(2,2-bis-hydroxymethyl-butoxy)-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, octanoic acid 2-[(3-octanoylsulfanyl-propyl)-ethoxy-(2,2-bis-hydroxymethyl-butoxy)-silanyloxymethyl]-2-[(2,2-bis-hydroxymethyl-butoxy)-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butyl ester, and octanoic acid 2-[ethoxymethyl-(2,2-bis-octanoyloxymethyl-butoxy)-(3-octanonylsulfanyl-propyl)-silanyloxymethyl]-2-[(2,2-bis-aoctanoyloxymethyl-butoxy)-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butyl ester.

9. The partial to substantially complete hydrolyzate(s) of sulfur-containing silane of general Formula (1) of claim 1 .

10. A process for preparing sulfur-containing silane prepared by the process which comprises reacting

a) at least one sulfur-containing silane of general Formulae (2), (3), (4), (5) and (6):

(Y 1 S)-G 1 -(SiX 1 X 2 X 3 )   (2)

(Y 2 S)-G 2 -(SiX 1 X 2 X 3 )   (3)

(Y 3 S)-G 3 -(SiX 1 X 2 X 3 )   (4)

(Y 4 S)-G 4 -(SiX 1 X 2 X 3 )   (5)

(Y 5 S)-G 5 -(SiX 1 X 2 X 3 )   (6)

wherein:

each occurrence of G 1 , G 2 , G 3 , G 4 and G 5 is independently a hydrocarbylene group containing from 1 to 15 carbon atoms selected from the group consisting of alkylene, alkenylene, arylene, or aralkylene;

each occurrence of X 1 is independently selected from the group consisting of —Cl, —Br, R 3 O—, R 3 C(═O)O—, R 3 2 C═NO—, and R 3 2 NO—, wherein each R 3 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 30 carbon atoms;

each occurrence of X 2 and X 3 is independently selected from the group consisting of —Cl, —Br, R 3 O—, R 3 C(═O)O—, R 3 2 C═NO—, R 3 2 NO— and R, wherein each occurrence of R is independently selected from the group consisting of straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing from 1 to 12 carbon atoms, and each occurrence of R 3 is independently selected from the group consisting of hydrogen and straight, cyclic and branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 30 carbon atoms;

each occurrence of Y 1 , Y 2 , Y 3 , Y 3 , and Y 5 is independently selected from the group consisting of hydrogen and an acyl group, R 3 C(═O)—, wherein each occurrence of R 3 is independently selected from the group consisting of hydrogen, straight, cyclic and branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 30 carbon atoms; with

b) one or more dihydroxyl-containing compounds of general Formula (7):

R 1 A 1 C(═O)A 2 G 6 (OH) 2 ,   (7)

wherein A 1 is selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group, an oxygen atom and —NR 2 —; A 2 is selected from the group consisting of a covalent chemical bond between G 6 and the carbonyl group, oxygen atom and —NR 2 —; R 1 is selected from the group consisting of hydrogen and straight, cyclic and branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; R 2 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; and, G 6 is a hydrocarbylene group of from 3 to 15 carbon atoms; thereby producing sulfur-containing silane of Formula (1).

11. The process of claim 10 wherein the sulfur-containing silane(s) of Formulae (2) to (6) are further reacted with one or more monohydroxyl-containing compounds of general Formula (8):

[R 1 A 1 C(═O)A 2 ] 2 G 6 OH,   (8)

wherein each occurrence of A 1 is independently selected from the group consisting of a covalent chemical bond between R 1 and the carbonyl group, oxygen atom and —NR 2 —; each occurrence of A 2 is independently selected from the group consisting of a covalent chemical bond between G 6 and the carbonyl group, an oxygen atom and —NR 2 —; each occurrence of R 1 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; each occurrence of R 2 is independently selected from the group consisting of hydrogen and straight, cyclic or branched alkyl, alkenyl, aryl, and aralkyl groups containing up to 18 carbon atoms; and, G 6 is a hydrocarbylene group of from 3 to 15 carbon atoms.

12. The process of claim 10 wherein the sulfur-containing silane(s) of Formulae (2) to (6) are further reacted with one or more dihydroxyl- and/or trihydroxyl-containing compounds of general Formula (9):

H-A 2 G 6 (OH) 2   (9)

wherein A 2 is selected from the group consisting of an oxygen atom and —NR 2 — wherein R 2 is selected from the group consisting of hydrogen and straight, cyclic and branched alkyl, akenyl, aryl, and aralkyl groups containing up to 10 carbon atoms; and, G 6 is independently a hydrocarbylene group of from 3 to 15 carbon atoms.

13. The process of claim 10 wherein the process is carried out in a continuous operation which comprises:

a) reacting, in a thin film reactor, a thin film reaction medium comprising a mixture of at least one silane of Formulae (2), (3), (4) (5) and/or (6) with at least one polyhydroxy-containing compound of Formula (7), optionally of Formulae (8) and/or (9), and optionally a transesterification catalyst, to provide silane(s) that contain a cyclic and/or bridged dialkoxy group, and by-product monoalcohol;

b) vaporizing by-product monoalcohol from the thin film to drive the reaction;

c) optionally, recovering by-product monoalcohol;

d) recovering reaction product(s); and,

e) optionally, neutralizing the reaction medium to increase the storage stability of the silane product(s) therein.

14. The process of claim 10 wherein the reaction is carried out at a temperature ranging from 0 to 200° C. while maintaining a pressure in the range of from 0.1 to 2000 mm Hg absolute.

15. The process of claim 10 carried out in the presence of a catalytically effective amount of at least one transesterification catalysts.

16. The process of claim 10 wherein the process provides at least one sulfur-containing silane product selected from the group consisting of hexanoic acid 2-(3-butyrylsulfanyl-propyl)-5-ethyl-2-methyl-[1,3,2]dioxasilinan-5-yl ester, hexanoic acid 2-(3-butyrylsulfanyl-propyl)-5-ethyl-2-ethoxy-[1,3,2]dioxasilinan-5-yl ester, hexanoic acid 2-(3-butyrylsulfanyl-propyl)-2-(3-hexanoyloxy-4-hydroxy-propoxy)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(3-hexanoyloxymethyl-4-hydroxy-3-methyl-propoxy)-2-(3-hexanoylsulfanyl-propyl)-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 2-(3-hexanoyloxymethyl-4-hydroxy-3-methyl-propoxy)-2-(3-mercapto-propyl)-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, 2-ethyl-hexanoic acid 2-[3-(2-ethyl-hexanoyloxymethyl)-4-hydroxy-3 -methyl-propoxy]-2-[3-(2-ethyl-hexanoylsulfanyl)-propyl]-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, 2-ethyl-hexanoic acid 2-[4-(2-ethyl-hexanoyloxy)-3-methyl-butoxy]-2-[3-(2-ethyl-hexanoylsulfanyl)-propyl]-5-methyl-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 5-ethyl-2-(3-mercapto-propyl)-2-methyl-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-ethoxy-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester,octanoic acid 2-(2,2-bis-hydroxymethyl-butoxy)-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-(2-hydroxymethyl-2-octanoyloxymethyl-butoxy)-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(2,2-bis-octanoyloxymethyl-butoxy)-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 2-(2,2-bis-octanoyloxymethyl-butoxy)-5-ethyl-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-(2-hydroxymethyl-2-octanoyloxymethyl-butoxy)-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-{2-[5-ethyl-5-hydroxymethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-2-yloxymethyl]-2-octanoyloxymethyl-butoxy}-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanoic acid 5-ethyl-2-{2-[5-ethyl-5-octanoyloxymethyl-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxymethyl]-2-octanoyloxymethyl-butoxy}-2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-5-yl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-(3-ethyl-3-methyl-heptanoylamino)-2-(octanoylamino-methyl)-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-octanoylamino-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexyloxycarbonyloxy-2-hexyloxycarbonyloxymethyl-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexyloxycarbonyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexylcarbarnoyloxy-2-hexylcarbamoyloxymethyl-3-[2-(3-octanoylsulfanyl-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexylcarbamoyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, octanethioic acid 3-(5-ethyl-2-{2-ethyl-4-hexylcarbamoyloxy-2-hexylcarbamoyloxymethyl-3-[2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-2-yloxy]-butoxy}-5-hexylcarbamoyloxymethyl-[1,3,2]dioxasilinan-2-yl)-propyl ester, acetic acid 2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, N-{2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl}-acetamide, carbonic acid 2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-[ethoxy-(3 -mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester propyl ester, thioacetic acid S-[3-(ethoxy-{2-[ethoxy-(4-mercapto-butyl)-methyl-silanyloxymethyl]-2-propoxycarbonyloxymethyl-butoxy}-methyl-silanyl)-propyl]ester, thioacetic acid S-[3-(ethoxy-{2-[ethoxy-(4-mercapto-butyl)-ethoxy-silanyloxymethyl]-2-propoxycarbonyloxymethyl-butoxy}-ethoxy-silanyl)-propyl]ester, acetic acid 2-{2-acetoxymethyl-2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-methyl-silanyloxymethyl]-butoxy}-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-ylmethyl ester, octanoic acid 2-{2-octanoyloxymethyl-2-[{2-octanoyloxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-octanonylsulfanyl-propyl)-methyl-silanyloxymethyl]-butoxy}-5-ethyl-2-(3-mercapto-propyl)-[1,3,2]dioxasilinan-5-ylmethyl ester, acetic acid 2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-ethoxy-silanyloxymethyl]-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, acetic acid 2-[{2-acetoxymethyl-2-[ethoxy-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butoxy}-(3-acetylsulfanyl-propyl)-methyl-silanyloxymethyl]-2-[(3-acetylsulfanyl-propyl)-ethoxy-methyl-silanyloxymethyl]-butyl ester, octanoic acid 2-[{2-octanoyloxymethyl-2-[ethoxy-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butoxy}-(3-octanoylsulfanyl-propyl)-methyl-silanyloxymethyl]-2-[(3-octanoylsulfanyl-propyl)-diethoxy-silanyloxymethyl]-butyl ester, acetic acid 2,2-bis-[(3-acetylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-methyl-silanyloxymethyl]-butyl ester, acetic acid 2,2-bis-[(3-acetylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-ethoxy-silanyloxymethyl]-butyl ester, octanoic acid 2-[(3-octanoylsulfanyl-propyl)-(2,2-bis-hydroxymethyl-butoxy)-ethyl-silanyloxymethyl]-2-[(2,2-bis-hydroxymethyl-butoxy)-(3-mercapto-propyl)-methyl-silanyloxymethyl]-butyl ester, octanoic acid 2-[(3-octanoylsulfanyl-propyl)-ethoxy-(2,2-bis-hydroxymethyl-butoxy)-silanyloxymethyl]-2-[(2,2-bis-hydroxymethyl-butoxy)-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butyl ester, and octanoic acid 2-[ethoxymethyl-(2,2-bis-octanoyloxymethyl-butoxy)-(3-octanonylsulfanyl-propyl)-silanyloxymethyl]-2-[(2,2-bis-aoctanoyloxymethyl-butoxy)-(3-mercapto-propyl)-ethoxy-silanyloxymethyl]-butyl ester.

17. Free-flowing particulate composition which comprises:

a) at least one particulate filler; and,

b) at least one silane of Formula (1) in admixture with and/or chemically bonded to particulate (a).

18. The free-flowing particulate composition of claim 17 wherein the particulate is at least one member selected from the group consisting of metal oxide, siliceous material and carbon black.

19. The free-flowing particulate composition of claim 18 wherein the metal oxide is at least one member selected from the group consisting of silica, titanium and alumina; and, the siliceous material is at least one member of the group consisting of aluminosilicate, clay and talc.

20. The free-flowing particulate composition of claim 19 wherein the particulate is at least one member selected from the group consisting of mixtures of silica and carbon black and mixtures of silica and alumina.

21. A rubber composition comprising (a) at least one rubber component, (b) at least one particulate filler and (c) at least one sulfur-containing silane of claim 1 .

22. An article of manufacture selected from the group consisting of tires, industrial goods, shoe soles, hoses, seals, gaskets and cable jackets of which at least one component is the cured rubber composition of claim 21 .

Assignments (20)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Mar 31, 2023
From: BNP PARIBAS
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063259/0133 →
RELEASE OF SECURITY INTEREST Recorded Mar 30, 2023
From: KOOKMIN BANK NEW YORK
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063197/0373 →
RELEASE OF SECURITY INTEREST Recorded Dec 24, 2020
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS COLLATERAL AGENT
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 054883/0855 →
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 →
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 →
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 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded May 21, 2019
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 050304/0555 →
RELEASE OF SECURITY INTEREST Recorded May 15, 2019
From: BOKF, NA
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 049249/0271 →
RELEASE OF SECURITY INTEREST Recorded May 15, 2019
From: BOKF, NA
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 049194/0085 →
NOTICE OF CHANGE OF COLLATERAL AGENT - ASSIGNMENT OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Mar 6, 2015
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. AS COLLATERAL AGENT
To: BOKF, NA, AS SUCCESSOR COLLATERAL AGENT
Reel/Frame 035136/0457 →
NOTICE OF CHANGE OF COLLATERAL AGENT - ASSIGNMENT OF SECURITY INTEREST IN INTELLECTUAL PROPERTY - SECOND LIEN Recorded Mar 6, 2015
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. AS COLLATERAL AGENT
To: BOKF, NA, AS SUCCESSOR COLLATERAL AGENT
Reel/Frame 035137/0263 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Oct 30, 2014
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 034113/0331 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Oct 30, 2014
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 034113/0252 →
SECURITY INTEREST Recorded Oct 27, 2014
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS COLLATERAL AGENT
Reel/Frame 034066/0662 →
SECURITY INTEREST Recorded Oct 27, 2014
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS COLLATERAL AGENT
Reel/Frame 034066/0570 →
SECURITY AGREEMENT Recorded Apr 29, 2013
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 030311/0343 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A., THE
Reel/Frame 030185/0001 →
SECURITY AGREEMENT Recorded May 31, 2012
From: MOMENTIVE PERFORMANCE MATERIALS INC
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A., THE
Reel/Frame 028344/0208 →
SECURITY AGREEMENT Recorded Jul 1, 2009
From: MOMENTIVE PERFORMANCE MATERIALS, INC.; JUNIPER BOND HOLDINGS I LLC; JUNIPER BOND HOLDINGS II LLC; JUNIPER BOND HOLDINGS III LLC; JUNIPER BOND HOLDINGS IV LLC; MOMENTIVE PERFORMANCE MATERIALS CHINA SPV INC.; MOMENTIVE PERFORMANCE MATERIALS QUARTZ, INC.; MOMENTIVE PERFORMANCE MATERIALS SOUTH AMERICA INC.; MOMENTIVE PERFORMANCE MATERIALS USA INC.; MOMENTIVE PERFORMANCE MATERIALS WORLDWIDE INC.; MPM SILICONES, LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS COLLATERAL TRUSTEE
Reel/Frame 022902/0461 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2008
From: HWANG, LESLEY; CHAVES, ANTONIO; POHL, ERIC R.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 021646/0912 →