Literature DB >> 35638632

Chain-Growth Polymerization of Benzotriazole Using Suzuki-Miyaura Cross-Coupling and Dialkylbiarylphosphine Palladium Catalysts.

Michael V Bautista1, Anthony J Varni1, Josué Ayuso-Carrillo1, Chia-Hua Tsai1, Kevin J T Noonan1.   

Abstract

Electron-deficient (n-type) conjugated materials are commonly prepared via step-growth methods with limited control over the molecular weight and molecular weight distribution of the resulting polymers. In this communication, we demonstrate that Pd-dialkylbiarylphosphine catalysts enable the chain-growth polymerization of benzo[1,2,3]triazole using Suzuki-Miyaura coupling with molecular weight control and modest molecular weight distributions (Đ ∼ 1.2-1.6). The importance of a free ligand in the reaction mixture during polymerization was established by analysis of polymer samples using GPC and MALDI-TOF mass spectrometry. A block copolymer with poly(3-hexylthiophene) was also synthesized by sequential monomer addition. The success of these commercially available catalysts for polymerization of benzotriazole highlights their potential for chain-growth reactions with other bicyclic arenes in the future.

Entities:  

Year:  2020        PMID: 35638632     DOI: 10.1021/acsmacrolett.0c00580

Source DB:  PubMed          Journal:  ACS Macro Lett        ISSN: 2161-1653            Impact factor:   6.903


  2 in total

1.  Ring walking as a regioselectivity control element in Pd-catalyzed C-N cross-coupling.

Authors:  Madeleine C Deem; Joshua S Derasp; Thomas C Malig; Kea Legard; Curtis P Berlinguette; Jason E Hein
Journal:  Nat Commun       Date:  2022-05-24       Impact factor: 17.694

2.  Synthesis, properties, and material hybridization of bare aromatic polymers enabled by dendrimer support.

Authors:  Shusei Fujiki; Kazuma Amaike; Akiko Yagi; Kenichiro Itami
Journal:  Nat Commun       Date:  2022-09-16       Impact factor: 17.694

  2 in total

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