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Porous, functional, poly(styrene-co-divinylbenzene) monoliths by RAFT polymerization

Version 2 2024-06-13, 10:55
Version 1 2017-09-25, 10:45
journal contribution
posted on 2024-06-13, 10:55 authored by KJ Barlow (nee Tan), X Hao, TC Hughes, OE Hutt, A Polyzos, KA Turner, G Moad
Herein we provide the first report of a new method for the preparation of porous functional poly(styrene-co-divinylbenzene) monoliths by use of reversible addition–fragmentation chain transfer (RAFT) polymerization. The method, exemplified by styrene–divinylbenzene copolymerization in the presence of 2-cyano-2-propyl dodecyl trithiocarbonate, provides control over polymerization kinetics, monolith morphology and surface functionality. Kinetic studies of monolith formation show a period of slow copolymerization, with a rate similar to RAFT homopolymerization of styrene, followed by rapid copolymerization, with a rate similar to that observed in conventional styrene–divinylbenzene copolymerization. The time to onset of rapid polymerization (gelation) and the monolith morphology depend strongly on the RAFT agent concentration. The RAFT-synthesized monoliths show a modified morphology with smaller pores and polymer globules when compared to non-RAFT monoliths, but importantly retain good flow properties. Retention of the thiocarbonylthio group within the monolith structure in an active form for surface-functionalization of the polymeric monoliths is demonstrated by the successful RAFT “grafting from” polymerization of (4-vinylphenyl)boronic acid. These functional monoliths have potential applications in chromatography and flow chemistry.

History

Journal

Polymer Chemistry

Volume

5

Pagination

722-732

Location

Cambridge, Eng.

ISSN

1759-9954

eISSN

1759-9962

Language

eng

Publication classification

C Journal article, C1.1 Refereed article in a scholarly journal

Copyright notice

2014, Royal Society of Chemistry

Issue

3

Publisher

Royal Society of Chemistry