Ready access to end-functional polystyrenes via a combination of ARGET ATRP and thiol–ene chemistry1. Issue 39 (21st October 2015)

• Record Type: Journal Article
• Authors: Altintas, Ozcan; Josse, Thomas; De Winter, Julien; Matsumoto, Nicholas M.; Gerbaux, Pascal; Wilhelm, Manfred; Barner-Kowollik, Christopher
• Is Part Of: Polymer chemistry. Volume 6:Issue 39(2015)
• Page Start: 6931
• Page End: 6935
• Publication Date: 2015-10-21
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c5py01048a
• Languages: English
• ISSNs: 1759-9954

Abstract

<abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgkgnhjxxb" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />Bromine end-groups of ATRP polystyrenes were converted into terminal alkene groups <italic>via</italic> a facile synthetic strategy. Subsequently, a light-induced radical thiol–ene reaction was employed for the functionalization of the terminal double bonds.</p> </abstract>