Thio-click modification of poly [2-(3-butenyl)-2-oxazoline]

Thio-click modification of poly [2-(3-butenyl)-2-oxazoline]
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DOI:
10.1021/ma071357r
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发表时间:
2007-10-30
期刊:
影响因子:
5.5
通讯作者:
Schlaad, Helmut
Schlaad, Helmut
中科院分区:
化学1区
文献类型:
--
作者:
Gress, Anja;Volkel, Antje;Schlaad, Helmut

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硫醇(RSH)自由基加成到聚[2-(3-丁烯基)-2-恶唑啉]上可以通过活性/受控的阳离子异构化聚合来获得,可以在不存在副反应的情况下顺利进行,表现出点击反应的特征。“硫代点击”反应可以在可行的([RSH]/[C=C]类似于1.2-1.5,无过渡金属添加剂)和温和的条件(在室温下用UV光产生自由基)下进行,并在一天内完成。疏水性含氟聚合物可以以与水溶性(共)聚合物或含糖共聚物相同的方式从容易获得的材料开始制备。
The radical addition of mercaptans (RSH) onto poly [2-(3-butenyl)-2-oxazoline], which is available through a living/controlled cationic isomerization polymerization, can proceed smoothly in the absence of side reactions, exhibiting the characteristics of a click reaction. The "thio-click" reaction can be performed under feasible ([RSH]/[C=C] similar to 1.2-1.5, no transition metal additives) and mild conditions (generation of radical's with UV light at room temperature) and goes to completion within a day. Hydrophobic fluoropolymers can be prepared in the same way as water-soluble (co-)polymers or glycopolymers, starting from readily available materials.