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作 者:Pengfei Sun Sichao Tian Mingchang Lin Guosong Chen
机构地区:[1]Key Laboratory for Organic Electronics and Information Displays & Institute of Advanced Materials, Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing University of Posts & Telecommunications [2]The State Key Laboratory of Molecular Engineering of Polymers and Department of Macromolecular Science, Fudan University
出 处:《Science China Chemistry》2018年第1期71-75,共5页中国科学(化学英文版)
基 金:supported by the National Natural Science Foundation of China (21604042, 21504016, 91527305);the Natural Science Foundation of Jiangsu Province of China (BK20150843);NUPTSF (NY215017, NY215080)
摘 要:This work investigated the effect of glyco-regioisomerism of glycopolymers on their dynamic interaction with benzoxaborole-containing polymers. Two kinds of glycopolymers, P-1-Gal and P-6-Gal, i.e. galactoside pendant group linked to the identical main chain through its anomeric(C1) and C6-hydroxyl group position, respectively, were studied. We found that P-6-Gal showed stronger binding strength to the PNIPAM-co-PBOB polymer than P-1-Gal did, which controlled the macroscopic property of the resultant hydrogels at a molecular level.This work investigated the effect of glyco-regioisomerism of glycopolymers on their dynamic interaction with benzoxaborole-containing polymers. Two kinds of glycopolymers, P-1-Gal and P-6-Gal, i.e. galactoside pendant group linked to the identical main chain through its anomeric (C1) and C6-hydroxyl group position, respectively, were studied. We found that P-6-Gal showed stronger binding strength to the PNIPAM-co-PBOB polymer than P-1-Gal did, which controlled the macroscopic property of the resultant hydrogels at a molecular level.
关 键 词:glyco-regioisomerism benzoxaborole GLYCOPOLYMERS hydrogel GLUCOSE
分 类 号:N0[自然科学总论—科学技术哲学]
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