Rapid Access to 2,2'-Bithiazole-Based Copolymers via Sequential Palladium-Catalyzed C-H/C-X and C-H/C-H Coupling Reactions

Macromol Rapid Commun. 2016 May;37(9):794-8. doi: 10.1002/marc.201600028. Epub 2016 Mar 22.

Abstract

A rapid access to 2,2'-bithiazole-based copolymers has been developed on the basis of the sequential palladium-catalyzed CH/CX and CH/CH coupling reactions. To assemble a "copolymer" through homopolymerization, a type of symmetric A-B-A-type building block is designed as the monomer and prepared via the regioselective C5H arylation of thiazole. A PdCl2 /CuCl-cocatalyzed oxidative CH/CH homopolymerization has been established to afford the 2,2'-bithiazole-based copolymers with high Mn (up to 69400). The current protocol features atom- and step-economy and exhibits a potential in the highly efficient construction of conjugated copolymers.

Keywords: 2,2′-bithiazole-based copolymers; oxidative CH/CH arylation polymerization; palladium-catalysis.

MeSH terms

  • Catalysis
  • Copper / chemistry*
  • Palladium / chemistry*
  • Polymers / chemical synthesis*
  • Polymers / chemistry
  • Thiazoles / chemistry*

Substances

  • Polymers
  • Thiazoles
  • Palladium
  • Copper
  • palladium chloride