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Hetero‐Functional Polymers with Alternating Hydroxyl and Epoxy Groups Synthesized by Thiol‐yne Click (co)Polymerization
Author(s) -
Zheng Yaochen,
Zhang Qian,
Gao Zhengguo,
Li Fucun,
Yan Bingfei,
Li Wenzuo
Publication year - 2018
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201800144
Subject(s) - polymerization , functional group , polymer chemistry , density functional theory , chemistry , thiol , polymer , epoxy , gel permeation chromatography , click chemistry , functional polymers , end group , computational chemistry , organic chemistry
A new family of hetero‐functional polythioethers with alternating hydroxyl and epoxy groups are facilely synthesized via photo‐initiated thiol‐yne click (co)polymerization under mild reaction conditions. Their chemical structures and hetero‐functional group density can be finely tuned by adjusting the feeding mole ratios. As the evidence of nuclear magnetic resonance and gel permeation chromatography tests shows, either the molecular weight or the hetero‐functional group density depend greatly on the SH bond cleavage energy of dithiols which can be predicted by theoretical calculation, using the density functional theory (DFT) with B3LYP hybrid functional and the QCISD methods. This paper provides access to a wide range of new materials with a specific structure and plentiful alternating hetero‐functional groups. Moreover, it unveils and highlights the role of SH bond cleavage energy of dithiols during the process of step‐growth thiol‐yne click (co)polymerization.