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

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Publication year
2004Source
Polymer : the International Journal for the Science and Technology of Polymers, 45, 22, (2004), pp. 7417-7430ISSN
Publication type
Article / Letter to editor

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Organization
Physical Organic Chemistry
Synthetic Organic Chemistry
Former Organization
Physical Organic and Supramolecular Chemistry
Journal title
Polymer : the International Journal for the Science and Technology of Polymers
Volume
vol. 45
Issue
iss. 22
Page start
p. 7417
Page end
p. 7430
Subject
Physical Organic ChemistryAbstract
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.
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