4.2 Article

Investigation of Thiol-ene Addition Reaction on Poly(isoprene) Under UV Irradiation: Synthesis of Graft Copolymers with V-Shaped Side Chains

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 48, Issue 17, Pages 3797-3806

Publisher

WILEY
DOI: 10.1002/pola.24164

Keywords

atom transfer radical polymerization (ATRP); esterification; graft copolymers; poly(isoprene); thiol-ene addition reaction; UV-irradiation

Funding

  1. Natural Science Foundation of Shanghai [08ZR1400800]
  2. Natural Science Foundation of China [20874013]

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Poly(isoprene) (PI) with pendant functional groups was successfully synthesized by thiol-ene addition reaction under 365 nm UV irradiation, and the functionalized PI was further modified and used to prepare graft copolymers with V-shaped side chains. First, the pendant -SCH2CH(OH)CH2OH groups were introduced to PI by thiol-ene addition reaction between 1-thioglycerol and double bonds, and the results showed that the addition reaction carried out only on double bonds of 1,2-addition isoprene units. After the esterification of hydroxyl groups by 2-bromoisobutyryl bromide, the forming macroinitiator was used to initiate the atom transfer radical polymerization (ATRP) of styrene (St) and tert-butyl acrylate (tBA), and the graft copolymers PI-g-PS2 and PI-g-PtBA(2) or PI-g-PAA(2) (by hydrolysis of PI-g-PtBA(2)) were obtained, respectively. It was confirmed that the graft density of side chains on PI main chains could be easily controlled by variation of the contents of modified 1,2-addition isoprene units on PI. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3797-3806, 2010

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