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            美國布魯克海文儀器公司>技術(shù)文章>測量應(yīng)用案例-62-200SM

            技術(shù)文章

            測量應(yīng)用案例-62-200SM

            閱讀:284          發(fā)布時(shí)間:2015-8-28
             文獻(xiàn)名: Construction and Self-Assembly of Single-Chain Polymer Nanoparticles via Coordination Association and Electrostatic Repulsion in Water
             
            作者: Zhengguang Zhu, Na Xu, Qiuping Yu, Lei Guo, Hui Cao, Xinhua Lu andYuanli Cai
            Suzhou Key Laboratory of Macromolecular Design and Precision Synthesis, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, China
             
            摘要:Simultaneous coordination-association and electrostatic-repulsion interactions play critical roles in the construction and stabilization of enzymatic function metal centers in water media. These interactions are promising for construction and self-assembly of artificial aqueous polymer single-chain nanoparticles (SCNPs). Herein, the construction and self-assembly of dative-bonded aqueous SCNPs are reported via simultaneous coordination-association and electrostatic-repulsion interactions within single chains of histamine-based hydrophilic block copolymer. The electrostatic-repulsion interactions are tunable through adjusting the imidazolium/imidazole ratio in response to pH, and in situ Cu(II)-coordination leads to the intramolecular association and single-chain collapse in acidic water. SCNPs are stabilized by the electrostatic repulsion of dative-bonded block and steric shielding of nonionic water-soluble block, and have a huge specific surface area of function metal centers accessible to substrates in acidic water. Moreover, SCNPs can assemble into micelles, networks, and large particles programmably in response to the solution pH. These unique media-sensitive phase-transformation behaviors provide a general, facile, and versatile platform for the fabrication of enzyme-inspired smart aqueous catalysts.
             
            關(guān)鍵詞:block copolymers;coordination;electrostatic interactions;self-assembly;single-chain nanoparticles

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