4.5 Review

Highly Efficient Catalysts for Direct Arylation Polymerization (DArP)

Journal

ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 7, Issue 7, Pages 1206-1216

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.201800227

Keywords

defect prevention; direct arylation; ligand control; palladium catalysts; polycondensation; pi-conjugated polymers

Funding

  1. KAKENHI from the Japan Society for the Promotion of Science [JP17H03055, JP23350042, JP17K05883, JP15K17855]
  2. ACT-C program of the Japan Science and Technology Agency
  3. Joint Usage/Research Center (JURC) at ICR, Kyoto University

Ask authors/readers for more resources

Recently, the palladium-catalyzed direct arylation polymerization (DArP) has emerged as a viable alternative to conventional synthetic means of making pi-conjugated polymers based on catalytic cross-coupling reactions. The DArP, which proceeds through C-H bond activation, has a distinct advantage over cross-coupling polymerization in terms of fewer reaction steps and higher functional group tolerance. We have developed novel catalysts for DArP by using P(2-MeOC6H4)(3) (L1) and P(2-Me2NC6H4)(3) (L2) as ligands. Although common direct arylation catalysts require the use of strongly coordinating solvents such as DMA and DMF, our catalysts exhibit high activity in THF and toluene, which are good solvents for pi-conjugated polymers. Thus, we could realize the precise synthesis of highly head-to-tail regioregular poly(3-hexylthiophene) (HT-P3HT) and donor-acceptor type alternating copolymers (DA polymers) with well-controlled structures through DArP.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available