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ATRPases: using nature's catalysts in atom transfer radical polymerizations
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1538259
Author(s) Kali, Gergely; Silva, Tilana B.; Sigg, Severin J.; Seidi, Farzad; Renggli, Kasper; Bruns, Nico
Author(s) at UniBasel Bruns, Nico
Sigg, Severin
Renggli, Kasper
Year 2012
Title ATRPases: using nature's catalysts in atom transfer radical polymerizations
Journal ACS symposium series
Volume 1100
Pages / Article-Number 171-181
Keywords atom transfer radical polymn horseradish peroxidase Hb laccase catalase
Abstract

Enzymes are environmentally friendly, non-toxic catalysts that have found many applications in synthetic polymer chem. However, until very recently no examples of enzyme-catalyzed, controlled radical polymns. were known. Here we review the nascent field of biocatalytic atom transfer radical polymn. (ATRP). The heme proteins horseradish peroxidase, Hb and catalase, as well as the copper-contg. enzyme laccase have been reported to display catalytic activity in activators regenerated by electron transfer (ARGET) ATRP of two model monomers, N-isopropylacrylamide and poly(ethylene glycol) Me ether acrylate. Bromine-terminated polymers, low polydispersity indexes, linear increase in mol. wt. with conversion as well as first-order kinetics indicate ATRP-type mechanisms. However, the first examples of biocatalytic ATRP also show that enzymes are much more complex catalysts than conventional ones.

Publisher American Chemical Society
ISSN/ISBN 0097-6156
edoc-URL http://edoc.unibas.ch/dok/A6083322
Full Text on edoc No
Digital Object Identifier DOI 10.1021/bk-2012-1100.ch011
ISI-Number WOS:000312966500011
Document type (ISI) Proceedings Paper
 
   

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