Transition-Metal-Free ipso-Arylative Condensation

被引:5
作者
Sinclair, Geoffrey S. [1 ,2 ]
Kukor, Andrew J. [1 ,2 ]
Imperial, Kevin Karl G. [1 ,2 ]
Schipper, Derek J. [1 ,2 ]
机构
[1] Univ Waterloo, Inst Polymer Res, Waterloo, ON N2L 3G1, Canada
[2] Univ Waterloo, Waterloo Inst Nanotechnol, Dept Chem, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CATALYZED DIRECT ARYLATION; HETEROAROMATIC CARBOXYLIC-ACIDS; CROSS-COUPLING REACTIONS; ARYL BOND FORMATION; C-C; DIRECT (HETERO)ARYLATION; DEPROTONATION MECHANISM; BAND-GAP; PALLADIUM; POLYMERIZATION;
D O I
10.1021/acs.macromol.0c00726
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The development of economical synthetic methods remains an important step toward the widespread use of conjugated polymers. Most well-established methods require either prefunctionalization with organometallic reagents or the use of expensive transition-metal catalysts. We have shown that 2-hydroxyalkyl- and 2-hydroxyaryl-substituted thiazole N-oxides can proceed through an ipso-arylative condensation that yields bithiazole-containing conjugated small molecules and polymers. The use of 2-hydroxyaryl substituents enables access to a wide scope of thiazole N-oxide substrates and presents an economical route to the synthesis of bithiazole-based conjugated polymers with varying physical and electronic properties.
引用
收藏
页码:5169 / 5176
页数:8
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