Facile synthesis of chain end functionalized polyethylenes via epoxide ring-opening and thiol–ene addition click chemistry
文献情報
Huayi Li, Jin-Yong Dong, Youliang Hu
A wide range of low-molecular-weight, narrow-molecular-weight-distribution chain end functionalized polyethylenes (Cef-PEs), including hydroxyl-, amino-, carboxyl-, sulfo-, chloro-, azide- and trimethoxysilane-terminated polyethylenes, were synthesized under mild conditions via epoxide ring-opening and thiol–ene addition reactions with epoxy- and vinyl-terminated PEs as starting materials, respectively. The selectivities of the functionalizations were excellent. Similarly, amphiphilic polyethylene-block-poly(ethylene glycol) copolymer (PE-b-PEG) was prepared for the first time by simply treating epoxy terminated PE with hydroxyl terminated PEG and potassium hydroxide. A unique combination of primary (hindered-phenol) and secondary (thioester) antioxidants was introduced into the chain end of PE via successive thiol–ene addition and transesterification reactions. All Cef-PEs were characterized unambiguously by NMR, GPC, DSC and FTIR.
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![[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure](https://static.chemtradehub.com/structs/100/100431-55-8-7104.webp)


