Literature DB >> 27145337

Double Modification of Polymer End Groups through Thiolactone Chemistry.

Frank Driessen1, Steven Martens1, Bernhard De Meyer1, Filip E Du Prez1, Pieter Espeel1.   

Abstract

A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of telechelic polymers is performed through amine-thiol-ene conjugation. Thiolactone end-functionalized polymers are prepared via two different methods, through controlled radical polymerization of a thiolactone-containing initiator, or by modification of available end-functionalized polymers. Next, these different linear polymers are treated with a variety of amine/acrylate-combinations in a one-pot procedure, creating a library of tailored end-functionalized polymers. End group conversions are monitored via SEC, NMR, and MALDI-TOF analysis, confirming the quantitative modification after each step. Finally, this strategy is applied for the synthesis of block copolymers via polymer-polymer conjugation and the successful outcome is analyzed via LCxSEC measurements.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amine-thiol-ene conjugation; end group functionalities; one-pot double modification; polymer-polymer conjugation

Mesh:

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Year:  2016        PMID: 27145337     DOI: 10.1002/marc.201600150

Source DB:  PubMed          Journal:  Macromol Rapid Commun        ISSN: 1022-1336            Impact factor:   5.734


  1 in total

1.  Polyoxazolines with a Vicinally Double-Bioactivated Terminus for Biomacromolecular Affinity Assessment.

Authors:  Florian Pinzner; Thorsten Keller; Jürgen Mut; Julian Bechold; Jürgen Seibel; Jürgen Groll
Journal:  Sensors (Basel)       Date:  2021-05-01       Impact factor: 3.576

  1 in total

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