IP Library Granted Patent US 10,858,377
Granted Patent B2
US 10,858,377 · App. 15/551,519 · Granted Dec 8, 2020

Multivinylaminosilanes as branching agents for functionalized elastomeric polymers

Inventors: Michael Rossle (Merseburg, DE); Christian Doring (Markranstadt, DE); Sven Thiele (Halle, DE); Dominique Thielemann (Leipzig, DE)
Assignee: TRINSEO EUROPE GMBH
C07F7/10C07F7/0801C07F7/21C08F36/06C08F36/08C08F236/10C08F293/005C08J3/24C08K3/04C08K3/36C08L9/06C08L21/00C08F230/08C08F2438/00C08F2810/20C08J2347/00
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Quick Facts
Patent No.
US 10,858,377
App. No.
15/551,519
Granted
Dec 8, 2020
Kind
B2
Abstract

Novel polymerizable multivinylaminosilanes which are useful as branching agents for synthetic and natural rubber are described. The compounds can be used in the polymerization of conjugated diene monomers, optionally together with aromatic vinyl monomers, thus producing polymers, which can favorably be used in rubber articles such as tires.

Claims (93)

1. A multivinylaminosilane which is a compound selected from

wherein

each B is independently selected from a group —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl, and

R is a C 1 -C 6 alkyl group;

or from one of Formulas 1-1, 1-3, 1-4 and 1-5:

wherein

each of R 11 , R 12 , R 13 , R 14 and R 15 is independently selected from C 1 -C 18 alkyl, C 6 -C 18 aryl, optionally C 1 -C 4 alkyl-substituted C 3 -C 12 heteroaryl, C 7 -C 18 aralkyl, —Si(R 6 )(R 7 )(R 8 ), wherein each of R 6 , R 7 and R 8 is independently selected from methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, and —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, butyl, hexyl, octyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl, and at least two of R 11 , R 12 , R 13 , R 14 and R 15 are —Si(R 1 )(R 2 )(R 3 ),

each of R 9 and R 19 is independently selected from ethylene (—C 2 H 4 —), propylene (—C 3 H 6 —) and butylene (—C 4 H 8 —), phenylene and —(CH 2 ) a′ —C 6 H 5 —(CH 2 ) b′ —, wherein each of a′ and b′ is an integer independently selected from 0 and 1, and

c is an integer selected from 0, 1, 2 and 3;

wherein

each B is independently selected from a group —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl,

each of R 20 , R 21 and R 22 is independently selected from a single bond and a C 1 -C 10 alkylene group,

d is an integer selected from 0, 1 and 2, and d′ is an integer selected from 0 and 1, wherein d is 0 when d′ is 0, and

each group —N< >X— is independently selected from a 5- to 10-membered heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein each X is independently selected from —N—, —C═ and —CH—, and heteroatomic groups other than the two groups N and X expressly shown in Formula 1-3 are selected from —N═, >NR 16 , —O—, —S— and >SiR 17 R 18 , wherein R 16 is selected from C 1 -C 6 alkyl, group B as defined above, phenyl and benzyl, wherein each of R 17 and R 18 is independently selected from C 1 -C 6 alkyl, phenyl and benzyl;

wherein

each B is independently selected from a group —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl,

D is a 5- to 10-membered carbocyclic or heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein in the heterocyclic group are selected from —N═, >NR 16 , —O—, —S— and >SiR 17 R 18 , wherein R 16 is selected from C 1 -C 6 alkyl, group B as defined above, phenyl and benzyl, and each of R 17 and R 18 is independently selected from C 1 -C 6 alkyl and phenyl,

each group —N< >X— is independently selected from a 5- to 10-membered heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein each X is independently selected from —N—, —C═ and —CH—,

R 23 is selected from a single bond and a C 1 -C 10 alkylene group, and

e is an integer selected from 2, 3 and 4;

wherein

each B is independently selected from a group —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl,

E is a 6- to 10-membered cycloaliphatic or aromatic group,

each R′ is independently selected from a single bond and C 1 -C 2 alkylene,

each R is independently selected from group B as defined above, C 1 -C 4 alkyl and benzyl, and

f is an integer selected from 2 and 3.

2. The multivinylaminosilane according to claim 1 , wherein in Formula 1-1, each of R 11 , R 12 , R 13 , R 14 and R 15 is independently selected from methyl and —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, ethyl, propyl, butyl, hexyl, octyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl; each of R 9 and R 19 is ethylene; c is an integer selected from 0, 1, 2 and 3; and at least two of R 11 , R 12 , R 13 , R 14 and R 15 are —Si(R 1 )(R 2 )(R 3 ).

3. The multivinylaminosilane according to claim 1 , which is selected from

wherein

each B is independently selected from —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, butyl, hexyl, octyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl, and

each R is independently selected from B as defined above, C 1 -C 6 alkyl and benzyl, and at least two of R 11 , R 12 , R 13 , R 14 an d R 15 are —Si(R 1 )(R 2 )(R 3 );

or from

wherein each B is as defined above and at least two of R 11 , R 12 , R 13 , R 14 and R 15 are —Si(R 1 )(R 2 )(R 3 ).

4. The multivinylaminosilane according to claim 1 , wherein in Formula 1-4 D is selected from cyclopentyl, cyclohexyl, phenyl and tetrahydrofuranyl; each group —N< >X— is selected from piperidinyl and piperazinyl; R 23 is a single bond; and e is an integer selected from 2 and 3.

5. The multivinylaminosilane according to claim 1 , wherein in Formula 1-5 E is selected from cyclohexyl and phenyl; R′ is a single bond; R is selected from group B as defined in claim 1 , C 1 -C 4 alkyl and benzyl; and f is an integer selected from 2 and 3.

6. A process for preparing the multivinylaminosilane as defined in claim 1 , the process comprising reacting an amine with a silane of the following Formula 2 in the presence of a base:

X—Si(R 1 )(R 2 )(R 3 )  (Formula 2)

wherein

X is selected from Cl, Br, I, trifluoromethanesulfonate (OTf) and tosylate (OTos),

R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl; and

the amine is a compound having at least two groups independently selected from a primary amino group and a secondary amino group.

7. An initiator compound obtainable by reacting a multivinylaminosilane of the following Formula 1 with an organo-alkali metal compound

(A)-B n   (Formula 1)

wherein

A is an organic group having at least two amino groups,

each B is independently selected from a group —Si(R 1 )(R 2 )(R 3 ), wherein R 1 , R 2 and R 3 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, with the proviso that at least one of R 1 , R 2 and R 3 is selected from vinyl and butadienyl, wherein each group B is a substituent of an amino group of group A,

at least two of the amino groups of group A are each substituted with at least one group B,

n is an integer of at least 2, and

all amino groups in group A are tertiary amino groups.

8. The initiator compound according to claim 7 , wherein the organo-alkali metal compound is selected from methyllithium, ethyllithium, n-butyllithium, s-butyllithium, t-octyllithium, isopropyllithium, phenyllithium, cyclohexyllithium, 2-butyllithium, 4-phenylbutyllithium, t-butyldimethylsilyloxypropyllithium, dialkylaminopropyllithium, N-morpholinopropyllithium, sodium biphenylide, sodium naphthalenide and potassium naphthalenide.

9. The initiator compound according to claim 7 , wherein the multivinylaminosilane is a compound selected from the following Formulas 1-1 to 1-5:

wherein

each of R 11 , R 12 , R 13 , R 14 and R 15 is independently selected from group B as defined in claim 7 , C 1 -C 18 alkyl, C 6 -C 18 aryl, optionally C 1 -C 4 alkyl-substituted C 3 -C 12 heteroaryl, C 7 -C 18 aralkyl, and —Si(R 6 )(R 7 )(R 8 ), wherein each of R 6 , R 7 and R 8 is independently selected from methyl, ethyl, propyl, butyl, hexyl, octyl, phenyl and benzyl, and wherein at least two of R 11 , R 12 , R 13 , R 14 and R 15 are group B,

each of R 9 and R 19 is independently selected from ethylene (—C 2 H 4 —), propylene (—C 3 H 6 —) and butylene (—C 4 H 8 —), phenylene and —(CH 2 ) a′ —C 6 H 5 —(CH 2 ) b′ —, wherein each of a′ and b′ is an integer independently selected from 0 and 1, and

c is an integer selected from 0, 1, 2 and 3;

wherein

group B is as defined in claim 7 ,

—N< >N— is a 5- to 18-membered heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein heteroatomic groups, if present in the heterocyclic group, other than the two N atoms expressly shown in Formula 1-2 are selected from —N═, >NR 16 , —O—, —S— and >SiR 17 R 18 , wherein R 16 is selected from group B as defined in claim 7 , C 1 -C 6 alkyl, phenyl and benzyl, and each of R 17 and R 18 is independently selected from C 1 -C 6 alkyl, phenyl and benzyl;

wherein

group B is as defined in claim 7 ,

each of R 20 , R 21 and R 22 is independently selected from a single bond and a C 1 -C 10 alkylene group,

d is an integer selected from 0, 1 and 2, and d′ is an integer selected from 0 and 1, wherein d is 0 when d′ is 0,

each group —N< >X— is independently selected from a 5- to 10-membered heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein each X is independently selected from —N—, —C═ and —CH—, and heteroatomic groups, if present in the heterocyclic group, other than the two groups N and X expressly shown in Formula 1-3 are selected from —N═, >NR 16 , —O—, —S— and >SiR 17 R 18 , wherein R 16 is selected from C 1 -C 6 alkyl, group B as defined in claim 7 , phenyl and benzyl, and each of R 17 and R 18 is independently selected from C 1 -C 6 alkyl, phenyl and benzyl;

wherein

group B is as defined in claim 7 ,

D is a 5- to 10-membered carbocyclic or heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein heteroatomic groups are selected from —N═, >NR 16 , —O—, —S— and >SiR 17 R 18 , wherein R 16 is selected from C 1 -C 6 alkyl, group B as defined in claim 7 , phenyl and benzyl, each of R 17 and R 18 is independently selected from C 1 -C 6 alkyl and phenyl,

each group —N< >X— is independently selected from a 5- to 10-membered heterocyclic group which may be saturated or unsaturated and which may be substituted on any carbon atom of the ring with a C 1 -C 6 alkyl group, wherein each X is independently selected from —N—, —C═ and —CH—,

R 23 is selected from a single bond and a C 1 -C 10 alkylene group, and

e is an integer selected from 2, 3 and 4;

wherein

group B is as defined in claim 7 ,

E is a 6- to 10-membered cycloaliphatic or aromatic group,

each R′ is independently selected from a single bond and C 1 -C 2 alkylene,

each R is independently selected from group B as defined in claim 7 , C 1 -C 4 alkyl and benzyl, and

f is an integer selected from 2 and 3.

10. The initiator compound according to claim 9 , wherein in Formula 1-1 each of R 11 , R 12 , R 13 , R 14 and R 15 is independently selected from group B as defined in claim 7 and methyl, each of R 9 and R 19 is ethylene, and c is an integer selected from 0, 1, 2 and 3.

11. The initiator compound according to claim 9 , wherein the multivinylaminosilane is selected from

wherein group B is as defined in claim 7 and R is independently selected from group B, C 1 -C 6 alkyl and benzyl;

wherein R is a C 1 -C 6 alkyl group and group B is as defined in claim 7 ; or

wherein B is as defined in claim 7 .

12. The initiator compound according to claim 9 , wherein in Formula 1-4 D is selected from cyclopentyl, cyclohexyl, phenyl and tetrahydrofuranyl; each group —N< >X— is selected from piperidinyl and piperazinyl; R 23 is a single bond; and e is an integer selected from 2 and 3.

13. The initiator compound according to claim 9 , wherein in Formula 1-5 E is selected from cyclohexyl and phenyl; R′ is a single bond; R is selected from group B as defined in claim 7 , C 1 -C 4 alkyl and benzyl; and f is an integer selected from 2 and 3.

14. A process for preparing a branched elastomeric polymer, the process comprising:

polymerizing at least one conjugated diene and a multivinylaminosilane of Formula 1 as defined in claim 7 in the presence of an initiator compound,

polymerizing at least one conjugated diene in the presence of an initiator compound according to claim 7 , or

reacting a living polymer, obtainable by anionically polymerizing at least one conjugated diene, with a multivinylaminosilane of Formula 1 as defined in claim 7 .

15. A branched elastomeric polymer obtainable by a process as defined in claim 14 .

16. A non-vulcanized polymer composition comprising the branched elastomeric polymer as defined in claim 15 and one or more further components selected from (i) components which are added to or formed as a result of the polymerization process used for making the polymer, (ii) components which remain after solvent removal from the polymerization process, and (iii) components which are added to the polymer after completion of the polymer manufacturing process.

17. The non-vulcanized polymer composition according to claim 16 which comprises one or more fillers.

18. The non-vulcanized polymer composition according to claim 16 , which comprises one or more vulcanizing agents.

19. A vulcanized polymer composition which is obtained by vulcanizing the non-vulcanized polymer composition as defined in claim 18 .

20. An article comprising at least one component formed from the vulcanized polymer composition as defined in claim 19 , wherein the article is selected from a tire, a tire tread, a tire side wall, a tire carcass, a belt, a gasket, a seal, a vibration damper, a footwear component, a golf ball and a hose.

21. A process for preparing a vulcanized polymer composition, the process comprising vulcanizing the non-vulcanized polymer composition as defined in claim 18 .

Assignments (3)
CHANGE OF NAME Recorded May 15, 2025
From: SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA SPOLKA JAWNA (CURRENTLY SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA)
To: SYNTHOS DWORY 7 SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA
Reel/Frame 071281/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2025
From: TRINSEO EUROPE GMBH
To: SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA SPOLKA JAWNA (CURRENTLY SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA)
Reel/Frame 070743/0153 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2017
From: ROSSLE, MICHAEL; DORING, CHRISTIAN; THIELE, SVEN; THIELEMANN, DOMINIQUE
To: TRINSEO EUROPE GMBH
Reel/Frame 043310/0318 →
Priority Claims (1)
EP 15155545 · Feb 18, 2015 · regional
Continuity (1)
Related Publication 20180030070A1 · Feb 1, 2018