IP Library Granted Patent US 10,301,400
Granted Patent B2
US 10,301,400 · App. 15/677,479 · Granted May 28, 2019

Method of making a functionalized elastomer

Inventors: Stefan Mecking (Constance, DE); Margaret Flook Vielhaber (Kent, OH); Hannes Leicht (Constance, DE); Julia Katharina Bauer (Pfullendorf, DE); Inigo Gottker genannt Schnetmann (Constance, DE)
Assignee: The Goodyear Tire & Rubber Company
C08F4/6383C08F4/545C08F36/04C07D209/82C07D233/00C07F3/02G01R33/46
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Quick Facts
Patent No.
US 10,301,400
App. No.
15/677,479
Granted
May 28, 2019
Kind
B2
Abstract

The present invention is directed to a method of making a functionalized elastomer, comprising the step of polymerizing monomers comprising a conjugated diene monomer in the presence of a lathanide-based coordination polymerization catalyst activated with a magnesium compound of formula 1 where R 1 is phenylene, or a linear or branched alkane diyl group containing 2 to 10 carbon atoms, or a combination of one or more phenylene groups and one or more linear or branched alkane diyl groups containing 1 to 10 carbon atoms; Q is of formula 2 or 3 where R 2 is phenyl, or a linear or branched alkyl group containing 2 to 10 carbon atoms; where R 3 and R 4 are independently phenyl or a linear or branched alkyl group containing 1 to 10 carbon atoms, or R 2 and R 3 taken together with the nitrogen atom represent a nitrogen containing heterocyclic group containing from 4 to 12 carbon atoms.

Claims (18)

1. A method of making a functionalized elastomer, comprising the step of:

polymerizing a conjugated diene monomer in the presence of a lathanide-based coordination polymerization catalyst activated with a magnesium compound of formula 1

where R 1 is phenylene, or a linear or branched alkane diyl group containing 2 to 10 carbon atoms, or a combination of one or more phenylene groups and one or more linear or branched alkane diyl groups containing 1 to 10 carbon atoms;

Q is of formula 2 or 3

where R 2 is phenyl, or a linear or branched alkyl group containing 2 to 10 carbon atoms; and

where R 3 and R 4 are independently phenyl or a linear or branched alkyl group containing 1 to 10 carbon atoms, or R 3 and R 4 taken together with the nitrogen atom represent a nitrogen containing heterocyclic group containing from 4 to 12 carbon atoms.

2. The method of claim 1 , wherein the magnesium compound of formula 1 is selected from the group consisting of

3. The method of claim 1 , wherein the lanthanide-based catalyst is selected from neodymium borohydride complexes and neodymium carboxylates.

4. The method of claim 1 , wherein the lanthanide-based catalyst comprises Nd(BH 4 ) 3 .(THF) 3 .

5. The method of claim 1 , wherein the conjugated diene monomer is selected from the group consisting of 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, piperylene, 3-butyl-1,3-octadiene, and 2-phenyl-1,3-butadiene.

6. The method of claim 5 , wherein the monomer further comprises a functionalized monomer of formula 4

wherein R 6 is a covalent bond, phenylene, a linear or branched alkane diyl group containing 1 to 10 carbon atoms, or a combination of one or more phenylene groups and one or more linear or branched alkane diyl groups containing 1 to 10 carbon atoms; R 7 is hydrogen or a linear or branched alkyl group containing 1 to 10 carbon atoms; X 1 is selected from formulas 5 and 6

wherein R 8 and R 9 are independently trialkylsilyl, phenyl or a linear or branched alkyl group containing 1 to 10 carbon atoms, or one of R 8 and R 9 is hydrogen and the other is phenyl or a linear or branched alkyl group containing 1 to 10 carbon atoms, or R 8 and R 9 taken together with the nitrogen atom represent a nitrogen containing heterocyclic group containing from 4 to 12 carbon atoms; and X 2 is a sulfur atom or a structure of formula 7 or 8

wherein when X 2 is of formula 8, the S atom of formula 8 is adjacent to the phenyl ring of formula 6 and the N atom of formula 8 is adjacent to R 6 .

7. The method of claim 1 , further comprising the step of terminating the polymerization with a functional terminator substituted with a functional group comprising at least one heteroatom selected from phosphorus, boron, oxygen, halogens and silicon.

8. The method of claim 7 wherein the functional terminator comprises at least one functional group selected from the group consisting of phosphane, phosphonic acid, phosphate, phosphodiester, phosphotriester, silyl, alklysilyl, alkoxysilyl, and siloxy.

9. The method of claim 7 , wherein the functional terminator comprises a terminator selected from the group consisting of tetraethoxysilane, n-octyltriethoxysilane, 3-chloropropyltriethoxysilane, and chlorodiphenylphosphine.

10. The method of claim 1 , wherein the nitrogen containing heterocyclic group is selected from the group consisting of the structures.

Assignments (4)
SECURITY INTEREST Recorded Dec 10, 2025
From: G-3 CHICKADEE PURCHASER, LLC
To: MIZUHO BANK, LTD., AS ADMINISTRATIVE AGENT
Reel/Frame 073900/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2025
From: THE GOODYEAR TIRE & RUBBER COMPANY
To: G-3 CHICKADEE PURCHASER, LLC
Reel/Frame 073591/0677 →
SECURITY INTEREST Recorded Oct 31, 2025
From: G-3 CHICKADEE PURCHASER, LLC
To: FORTRESS CREDIT CORP., AS ADMINISTRATIVE AGENT
Reel/Frame 073439/0048 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2017
From: MECKING, STEFAN; VIELHABER, MARGARET FLOOK; BAUER, JULIA KATHARINA; LEICHT, HANNES; SCHNETMANN, INIGO GOTTKER GENANNT
To: GOODYEAR TIRE & RUBBER COMPANY, THE
Reel/Frame 043297/0242 →
Continuity (1)
Related Publication 20190055325A1 · Feb 21, 2019