副教授 博士生导师 硕士生导师
性别: 男
毕业院校: 大连理工大学
学位: 博士
所在单位: 化工学院
学科: 高分子材料. 高分子化学与物理. 功能材料化学与化工
办公地点: 西部校区化工实验楼A303
联系方式: 办公室电话:84986101,13610963135
电子邮箱: zhangchq@dlut.edu.cn
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发表时间: 2008-01-01
发表刊物: 化学进展
卷号: 20
期号: 11
页面范围: 1726-1732
ISSN号: 1005-281X
摘要: Novel methods of fine tuning initiation, activation, and deactivation processes for atom transfer radical polymerization (ATRP) are reviewed, including reverse ATRP, simultaneous reverse and normal initiation (SR&NI) ATRP, activators generated by electron transfer (AGET) ATRP, activators regenerated by electron transfer (ARGET) ATRP and initiators for continuous activator regeneration (ICAR) ATRP. These new systems gradually circumvent the oxidation problem of normal ATRP system and employ small amount of catalysts in the higher oxidation state, especially the latter two initiation systems whereby only minor amount (1-50ppm) of high-oxidation-state transition metal complex is needed to mediate polymerization and therefore greatly simplify the commercial procedures of ATRP method, making it to be applicable for industrial production. In addition, two novel catalyst systems for ATRP system, hybrid and bimetallic catalyst systems developed on the basis of immobilized catalyst, are thoroughly introduced. Both of them show high catalytic activity and capability to control the polymerization reaction and can be removed mostly by simple filtration or precipitation.
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