电化学调制表面引发原子转移自由基聚合的现场SPR研究

项目名称： 电化学调制表面引发原子转移自由基聚合的现场SPR研究

项目编号： No.21273173

项目类型： 面上项目

立项/批准年度： 2013

项目学科： 数理科学和化学

项目作者： 胡卫华

作者单位： 西南大学

项目金额： 80万元

中文摘要： 原子转移自由基聚合（ATRP）通过过渡金属络合物激活剂/钝化剂这一氧化还原电对调控引发剂在活性自由基与休眠态之间的快速转化和可逆平衡，实现活性/可控自由基聚合。采用电化学方法控制该氧化还原电对的相互转化是调控ATRP的可行方法（science 2011, 332, 81），但由于缺乏实时在线的研究手段，对这一过程的研究还不深入。本项目在前期工作的基础上，拟采用电化学－SPR联用技术，对电化学调制表面引发ATRP进行现场研究。具体来说：在金电极表面固定引发剂，采用电化学手段对电极表面的激活剂/钝化剂进行快速氧化还原调制，从而控制表面引发ATRP的进行；采用实时在线SPR技术现场监控表面引发ATRP对电化学调制的响应，深入研究电化学调制表面引发ATRP的基本规律。本项目有望建立一个全新的ATRP实时研究平台，开发一种制备聚合物刷的电化学方法，亦将加深对电化学调制ATRP过程的科学认识。

中文关键词： 表面引发原子转移自由基聚合；电化学调制；表面等离子体共振；激活剂/钝化剂电对；过渡金属络合物

英文摘要： Atom transfer radical polymerization (ATRP) is a controlled/living polymerization technique by activating a dormant alkyl halide initiator to form an active radical capable of chain propagation with a certain transition-metal complex activator, which is then reversibly oxidized to a deactivator. Using the activator/deactivator redox pair to build a dynamic equilibrium between the active radical and the dormant species and to minimize the irreversible bimolecular termination, ATRP allows for precise control over the polymer molecular weights, molecular weight distributions, and complex architectures, and has been extensively employed for polymer synthesis in a wide variety of applications. Electrochemical reduction of the deactivor to the activator is proved to be a feasible route to trigger and regulate the bulk ATRP (Science 2011, 332, 81). However, so far few is known concerning the exact process of electrochemically modulated ATRP due to the absence of both fast electrochemical modulation method and real-time study technique. In this project, we propose an in situ electrochemical surface plasmon resonance (SPR) technique, based on our previous work, to study this interesting phenomenon and further deepen our understanding on it. In details, the ATRP initiator is attached on the surface of SPR gold chip, and t

英文关键词： surface-initiated atom transfer radical polymeriza；electrochemical modulation；surface plasmon resonance；activator/deactivator redox pair；transition-metal complex