Synthesis, characterization and aggregation behavior of block copolymers containing a polyisocyanopeptide segment

被引:12
作者
Cornelissen, JJLM
Fischer, M
van Waes, R
van Heerbeek, R
Kamer, PCJ
Reek, JNH
Sommerdijk, NAJM
Nolte, RJM
机构
[1] Univ Nijmegen, NSRIM Inst, Dept Organ Chem, NL-6525 ED Nijmegen, Netherlands
[2] Univ Amsterdam, Inst Mol Chem, NL-1012 WX Amsterdam, Netherlands
[3] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
关键词
polymer chemistry; self organization;
D O I
10.1016/j.polymer.2004.08.067
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Following up on previous preliminary communications the synthesis of a series of block copolymers by applying amine end-capped polymers as initiators for the nickel(II) catalyzed polymerization of isocyanides is reported. Using a polystyrene derivative as the initiator, superamphiphiles containing a hydrophobic polystyrene tail and a charged helical polyisocyanide headgroup were prepared. Under proper conditions these superamphiphiles self-assembled in water to give a variety of aggregate morphologies, among which are superhelical architectures. Initiators derived from carbosilane dendritic wedges gave block copolymers with a unique combination of structural elements, i.e. a flexible dendritic block and a rigid polyisocyanide block. Block copolymers derived from the 3rd generation dendrimers form welldefined micellar aggregates in the presence of Ag+ ions. These aggregates have been used to construct nanoarrays of metallic silver. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7417 / 7430
页数:14
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