4.6 Article

Poly(N-isopropylacrylamide) hydrogels fabricated via click chemistry: well-defined alpha,omega-bis propargyl linear poly(N-isopropylacrylamide)s as crosslinkers

Journal

RSC ADVANCES
Volume 4, Issue 93, Pages 51510-51518

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra07987f

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Funding

  1. National Natural Science Foundation of China [21004005]

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A series of poly(N-isopropylacrylamide) (PNIPA) hydrogels were fabricated through click chemistry by using a well-defined azido-PNIPA carrying pendant azido groups, and linear alpha, omega-bis propargyl PNIPAs with different chain lengths. Here linear alpha, omega-bis propargyl PNIPAs were synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization by using a bis propargyl terminal chain transfer agent, whose chain lengths were modulated by changing polymerization conditions. The obtained hydrogels showed increasing ESR values in the swollen state and increasing volume phase transition temperatures (VPTTs) with increasing molecular weights of bis propargyl PNIPAs, ascribed to the lengthening distance between crosslinks and improving hydrophilicity. The incorporation of amine together with crosslinking modified the hydrophilicity of a click hydrogel, resulting in the elevated VPTT and additional pH sensitivity. The present study provided a facile method to regulate swelling properties and/or to impart special functions for PNIPA hydrogels, by adjusting the chain length of crosslinkers or by introducing other functional groups.

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