摘要
在 0~ 1 0 0℃温度范围内 ,由原子转移自由基聚合方法 ,采用助催化和非助催化体系 ,引发甲基丙烯酸甲酯聚合 ,利用 1 3 C NMR测定聚甲基丙烯酸甲酯的等规度 .发现原子转移自由基聚合仍以间同立构为主 ,随着聚合温度的升高间同立构等规度降低 ,与通常自由基聚合对有规立构控制特征相似 .助催化剂异丙醇铝和活性端羰基配位 ,对聚合物的立构规整性有一定的影响 .
Two series of PMMA samples have been synthesized by Atom Transfer Radical Polymerization(ATRP) with and without catalytic promoter(aluminum isopropoxide, ( i PrO) 3Al in the temperature range of 0~100 ℃. Their tacticity has been determined by 13 C Nuclear Magnetic Resonance(NMR). The results showed that the polymers by ATRP were all predominantly syndiotactic, and the tendency to form syndiotactic sequences decreased with the polymerization temperature increase. The tacticity of PMMA was influenced by catalytic promoter, [( i PrO) 3Al], because it coordinates with the ester carbonyl group of polymer chain end. The activation parameters governing the tacticity of ATRP were calculated. The results indicate that the same type of active species is present in ATRP and conventional radical system.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2000年第11期1762-1765,共4页
Chemical Journal of Chinese Universities
关键词
原子转移自由基聚合
等规度
甲基丙烯酸甲酯
Atom transfer radical polymerization
Tacticity
Poly(methyl methacrylate)
13 C NMR