IP Library Granted Patent US 6,844,407
Granted Patent B2
US 6,844,407 · App. 10/407,614 · Granted Jan 18, 2005

Control agents for living-type free radical polymerization, methods of polymerizing and polymers with same

Assignee: Symyx Technologies, Inc.
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Quick Facts
Patent No.
US 6,844,407
App. No.
10/407,614
Granted
Jan 18, 2005
Kind
B2
Abstract

Control agents that have a nitrogen-nitrogen bond covalently bonded to a thiocarbonyl moiety are provided for living-type free radical polymerization of a wide variety of monomers. These control agents provide superior properties for control of the polymerization and/or the properties of the polymers obtained and/or the monomers that may be polymerized. In some embodiments, a bulky group is pendant off the activated thiocarbonyl portion of the control agents. Multifunctional control agents provide the opportunity for a variety of structurally unique polymers, including block copolymers, stars and hyper-branched polymers.

Claims (23)

1. A compound characterized by the formula:

wherein R 1 is selected from the group consisting of hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl, and combinations thereof, with the proviso that R 1 is not methyl;

R 2 and R 3 are each independently selected from the group consisting of hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl, and combinations thereof;

R 4 is selected from the group consisting of hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and combinations thereof;

R 4 combines with R 2 and/or R 3 to form a ring structure, with said ring having from 3 to 50 non-hydrogen atoms.

2. The compound of claim 1 , wherein R 1 is selected from the group consisting of optionally substituted alkyl, optionally substituted aryl, optionally substituted alkenyl, optionally substituted alkoxy, optionally substituted heterocyclyl, optionally substituted alkylthio, optionally substituted amino and optionally substituted polymer chains.

3. The compound of claim 2 , wherein R 1 is selected from the group consisting of —CH 2 Ph, —CH(CH 3 )CO 2 CH 2 CH 3 , —CH(CO 2 CH 2 CH 3 ) 2 , —C(CH 3 ) 2 CN and —C(CH 3 ) 2 Ph.

4. The compound of claim 1 , wherein R 2 is hydrogen and R 3 and R 4 form a five member substituted heterocycle.

5. The compound of claim 4 , wherein the five member substituted heterocycle comprises a methyl substituent.

6. A compound characterized by the formula:

wherein R 1 is selected from the group consisting of hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl, and combinations thereof;

R 2 is hydrogen;

R 4 is selected from the group consisting of hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and combinations thereof; and

R 4 combines with R 3 to form a ring structure, with said ring having from 3 to 50 non-hydrogen atoms.

7. The compound of claim 6 , wherein R 1 is selected from the group consisting of optionally substituted alkyl, optionally substituted aryl, optionally substituted alkenyl, optionally substituted alkoxy, optionally substituted heterocyclyl, optionally substituted alkylthio, optionally substituted amino and optionally substituted polymer chains.

8. The compound of claim 7 , wherein R 1 is selected from the group consisting of —CH 2 Ph, —CH(CH 3 )CO 2 CH 2 CH 3 , —CH(CO 2 CH 2 CH 3 ) 2 , —C(CH 3 ) 2 , —C(CH 3 ) 2 CN and —C(CH 3 ) 2 Ph.

9. The compound of claim 6 , wherein R 4 and R 3 combine to form a substituted heterocycle.

10. The compound of claim 9 , wherein the heterocycle comprises at least one methyl substituent.

11. The compound of claim 9 , wherein the heterocycle comprises at least one oxygen substituent.

12. The compound of claim 9 , wherein the heterocycle comprises 5 non-hydrogen atoms.

13. The compound of claim 12 , wherein the heterocycle further comprises two methyl substituents.

14. The compound of claim 12 , wherein the heterocycle further comprises an oxygen substituent.

15. The compound of claim 13 , wherein the heterocycle further comprises a methyl substituent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2010
From: SYMYX SOLUTIONS, INC.
To: FREESLATE, INC.
Reel/Frame 024057/0911 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2009
From: SYMYX TECHNOLOGIES, INC.
To: SYMYX SOLUTIONS, INC.
Reel/Frame 022939/0564 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2003
From: CHARMOT, DOMINIQUE; CHANG, HAN TING; WANG, WENYUE
To: SYMYX TECHNOLOGIES, INC.
Reel/Frame 014145/0041 →
Continuity (3)
Division 0996317200 · Sep 25, 2001
Division 0967626700 · Sep 28, 2000
Related Publication 20040019163A1 · Jan 29, 2004