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作 者:Bin Yan Changyuan He Sheng Chen Li Xiang Lu Gong Yingchun Gu Hongbo Zeng
机构地区:[1]National Engineering Laboratory for Clean Technology of Leather Manufacture,College of Biomass Science and Engineering,Sichuan University,Chengdu 610065 [2]Department of Chemical and Materials Engineering,University of Alberta,Edmonton AB T6G 1H9
出 处:《CCS Chemistry》2022年第8期2724-2737,共14页中国化学会会刊(英文)
基 金:supports of the National Natural Science Foundation of China(no.21876119);Special Engineering Team of Sichuan University(no.2020SCUNG122);and Chengdu Science and Technology Program(no.2019-GH02-00029-HZ);H.Z.acknowledges the financial support from the Natural Sciences and Engineering Research Council of Canada(NSERC),Canada Foundation Innovation(CFI),and the Canada Research Chairs Program.
摘 要:Cation-πinteraction is considered one of the strongest noncovalent interactions in aqueous solutions,which endows natural biomolecules(e.g.,proteins)with robust wet adhesion and cohesion in humid/underwater environments.However,it remains a challenge to construct synthetic functional materials(e.g.,self-healing hydrogels)by adopting the cation-πinteractions rationally.Herein,we present a facile and novel strategy to fabricate injectable self-healing synthetic hydrogel from self-assembly of a thermoresponsive ABA triblock copolymer via cation-πinteractions.
关 键 词:cation-πinteraction SELF-HEALING INJECTABILITY HYDROGEL NANOCONFINEMENT
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