IP Library Granted Patent US 9,453,102
Granted Patent B2
US 9,453,102 · App. 14/518,951 · Granted Sep 27, 2016

Synthesis of chalcogen-capped pi-conjugated polymers

Inventors: Christine Keiko Luscombe (Seattle, WA); Ken Okamoto (Tsukuba, JP)
Assignee: University of Washington through its Center for Commercialization
C08G61/126C08G2261/1412C08G2261/16C08G2261/18C08G2261/312C08G2261/3142C08G2261/3221C08G2261/3223C08G2261/417C08G2261/70C08G2261/72C08G2261/964
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,453,102
App. No.
14/518,951
Granted
Sep 27, 2016
Kind
B2
Abstract

Methods for the preparation of mono- and bis-end-functionalized π-conjugated polymers. In the methods, chalcogens are selectively installed at the polymer terminus or termini.

Claims (16)

1. A method for mono-end-functionalizing a poly(arylene) with a chalcogen, comprising:

polymerizing an aryl monomer by reaction with a Grignard reagent and an aryl nickel catalyst to provide an aryl nickel complex-terminated poly(arylene); and

treating the aryl nickel complex-terminated poly(arylene) with a chalcogenating agent followed by treatment with an acid to provide a mono-chalcogen-end-functionalized poly(arylene).

2. The method of claim 1 , wherein the aryl monomer is selected from the group consisting of substituted and unsubstituted thiophenes, substituted and unsubstituted fluorenes, substituted and unsubstituted phenylenes, substituted and unsubstituted pyridines, and substituted and unsubstituted pyrroles.

3. A method for mono-end-functionalizing poly(3-hexylthiophene) with a chalcogen, comprising:

polymerizing a 3-hexylthiophene monomer by reaction with a Grignard reagent and an aryl nickel catalyst to provide an aryl nickel complex-terminated poly(3-hexylthiophene); and

treating the aryl nickel complex-terminated poly(3-hexylthiophene) with a chalcogenating agent followed by treatment with an acid to provide a mono-chalcogen-end-functionalized poly(3-hexylthiophene).

4. The method of claim 3 , wherein chalcogenating agent is elemental sulfur.

5. The method of claim 3 , wherein chalcogenating agent is selenium.

6. The method of claim 3 , wherein chalcogenating agent is carbon disulfide.

7. The method of claim 3 , wherein the aryl nickel complex-terminated poly(3-hexylthiophene) is treated with a chalcogenating agent and a base.

8. The method of claim 7 , wherein the base is a nitrogen base.

9. The method of claim 7 , wherein the base is 1,8-diazabicyclo[5.4.0]undec-7-ene.

10. The method of claim 3 , wherein the chalcogenating agent is in molar excess.

11. The method of claim 3 , wherein the aryl nickel complex-terminated poly(3-hexylthiophene) is an α-aryl-terminated ω-aryl nickel complex-terminated poly(3-hexylthiophene) prepared by initiating polymerization of the thiophene monomer with an aryl nickel initiator.

12. The method of claim 11 , wherein the aryl nickel initiator is (aryl)Ni(PPh 3 ) 2 Br.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 8, 2016
From: UNIVERSITY OF WASHINGTON
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 037470/0743 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2015
From: LUSCOMBE, CHRISTINE KEIKO; OKAMOTO, KEN
To: UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION
Reel/Frame 034760/0410 →
Continuity (2)
Provisional Application 61893075 · Oct 18, 2013
Related Publication 20150112028A1 · Apr 23, 2015