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作 者:Chao Li Xiqi Zhang Longfei Luo Lei Jiang Longcheng Gao
机构地区:[1]Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of Education,Key Laboratory of Beijing Energy,School of Chemistry,Beihang University,Beijing 100191 [2]Key Laboratory of Bio-Inspired Materials and Interfacial Science,Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Beijing 100190 [3]Beijing National Laboratory for Molecular Sciences,Key Laboratory of Polymer Chemistry and Physics of Ministry of Education,College of Chemistry and Molecular Engineering,Peking University,Beijing 100871
出 处:《CCS Chemistry》2022年第3期1065-1073,共9页中国化学会会刊(英文)
基 金:supported by the National Natural Science Foundation of China(nos.21875009 and 51973227);the National Key Research and Development Program of China(nos.2017YFA0206904 and 2017YFA0206900);the Youth Innovation Promotion Association CAS(no.2020028);the Fundamental Research Funds for the Central Universities。
摘 要:Mechanosensory elastomers attract intense interests in the academic and industrial fields.However,molecular insight of macroscopic properties remains a significant challenge.Herein,we build up a correlation between the microscopic and macroscopic level by designing a mechanosensory elastomer with aggregation-induced emission luminogens(AIEgens)that monitors chain deformation in situ.The key constituents are the mechanosensory units,which are dynamic dimers bonded by ureidopyrimidinone(UPy)groups and tetraphenylethylene(TPE)for the fluorescence signal output.The photoluminescence(PL)technique successfully monitors elastomer chain deformation under external forces.The PL intensity increases linearly at low elongation,in excellent agreement with Hooke’s law for ideal chains.Strong deviation from linear PL intensity is measured at high elongation,which can be theoretically described by the Langevin function.A correlation between the microscopic and the macroscopic level is then built.
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