C-H Activation as a Shortcut to Conjugated Polymer Synthesis

被引:44
作者
Blaskovits, J. Terence [1 ]
Leclerc, Mario [1 ]
机构
[1] Univ Laval, Dept Chem, Quebec City, PQ G1V 0A6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
C-H activation; conjugated polymer synthesis; direct (hetero)arylation polymerization; green chemistry; palladium catalysis; DIRECT ARYLATION POLYMERIZATION; DIRECT (HETERO)ARYLATION POLYMERIZATION; CATALYZED DIRECT ARYLATION; TRANSFER POLYCONDENSATION; COUPLING POLYMERIZATION; EFFICIENT APPROACH; PD; COPOLYMERS; THIOPHENE; DERIVATIVES;
D O I
10.1002/marc.201800512
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Direct (hetero)arylation polymerization exploits the palladium-catalyzed activation of aromatic C-H bonds for the atom-economical synthesis of conjugated polymers for a wide range of applications. This account outlines how direct arylation methodologies overcome many of the limitations of contemporary polymerization techniques at both the research and production scale, and explains how monomer design and reaction conditions must be tailored to ensure high polymer molecular weight, yield, and structural integrity. Current research aims to improve further this reaction's profile as a sustainable methodology while at the same time making it competitive with the Migita-Stille and Miyaura-Suzuki polymerizations both in scope of accessible structures and synthetic efficiency. This feature article charts the recent developments and future directions of C-H activation research as it moves toward becoming at once an industrially feasible, environmentally friendly, and synthetically powerful polymerization technique.
引用
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页数:15
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