4.7 Article

End Group-Functionalization and Synthesis of Block-Copolythiophenes by Modified Nickel Initiators

Journal

MACROMOLECULES
Volume 44, Issue 15, Pages 6017-6025

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma200846v

Keywords

-

Funding

  1. Katholieke Universiteit Leuven (GOA)
  2. Fund for Scientific Research (FWO-Vlaanderen)
  3. FRS-FNRS

Ask authors/readers for more resources

Polythiophenes with alcohol, tosylate, azide, ethynylene, carboxylic acid, and amine end groups were prepared by a combination of functionalized nickel initiators and postpolymerization reactions. The azide and ethynylene polymers were subsequently used in a click reaction to produce a conjugated block copolymer. Finally, a conjugated triblock-copolymer was synthesized by means of a chain growth polymerization initiated by a binuclear nickel initiator.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available