苯并噻二唑共轭有机分子合成研究进展  

Advance in Syntheses of 2,1,3- Benzothiadiazole conjugated compounds

作　　者：黄旦翔 夏萌[1] 彭雄伟[1] 黎太浩 程晓红[1] 

机构地区：[1]云南大学化学科学与工程学院,云南昆明650091

出　　处：《云南化工》2015年第6期28-35,47,共9页Yunnan Chemical Technology

基　　金：国家自然科学基金(No.21274119;NO.21364017);云南省自然科学基金(2013FA007);云南省教育厅科学基金(ZD2015001)

摘　　要：2,1,3-苯并噻二唑(BTD)共轭有机分子具有优异的光电特性,广泛应用于有机发光二极管、太阳能电池、液晶、荧光探针、光电管等方面。综述了以金属催化的偶联反应为关键步骤的2,1,3-苯并噻二唑(BTD)共轭有机分子的合成方法,包括Suzuki偶联反应,Stille偶合反应,Heck偶联反应,Sonogashir偶联反应,Nigishi偶联反应,Ullmann偶联反应等。2,1,3 - Benzothiadiazole conjugated compounds are one of the most active research area in the optoelectronic materials due to their outstanding optical and electrical properties and have great potentials as organic light - emitting diodes, solar cells, liquid crystals, fluorescent sensors and photovohaic cells ect. This review covers the various synthetic methods reported for 2,1,3 - Benzothiadiazole （BTD） conjugated compounds in recent years. Including Suzuki coupling reaction, Stille coupling reaction, Heck coupling reac- tion , Sonogashira coupling reaction, Nigishi coupling reaction, Ullmann coupling reaction ect.

关 键 词：2 1 3-苯并噻二唑 偶联反应 合成 

分 类 号：TN104.3[电子电信—物理电子学]