Huang Zhicheng, Gu Yu, Liu Xiaodong, Zhang Lifen, Cheng Zhenping, Zhu Xiulin
Suzhou Key Laboratory of Macromolecular Design and Precision Synthesis, Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China.
Macromol Rapid Commun. 2017 May;38(10). doi: 10.1002/marc.201600461. Epub 2016 Oct 28.
It is well known that the recently developed photoinduced metal-free atom transfer radical polymerization (ATRP) has been considered as a promising methodology to completely eliminate transition metal residue in polymers. However, a serious problem needs to be improved, namely, large amount of organic photocatalysts should be used to keep the controllability over molecular weights and molecular weight distributions. In this work, a novel photocatalyst 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) with strong excited state reduction potential is successfully used to mediate a metal-free ATRP of methyl methacrylate just with parts per million (ppm) level usage under irradiation of blue light emitting diode at room temperature, using ethyl α-bromophenyl-acetate as a typical initiator with high initiator efficiency. The polymerization kinetic study, multiple controlled "on-off" light switching cycle regulation, and chain extension experiment confirm the "living"/controlled features of this promising photoinduced metal-free ATRP system with good molecular weight control in the presence of ppm level photocatalyst 4CzIPN.
众所周知,最近开发的光诱导无金属原子转移自由基聚合(ATRP)被认为是一种有望完全消除聚合物中过渡金属残留的方法。然而,一个严重的问题需要改进,即需要使用大量的有机光催化剂来保持对分子量和分子量分布的可控性。在这项工作中,一种具有强激发态还原电位的新型光催化剂1,2,3,5-四(咔唑-9-基)-4,6-二氰基苯(4CzIPN)成功地用于在室温下蓝光发光二极管照射下,仅以百万分之一(ppm)水平的用量介导甲基丙烯酸甲酯的无金属ATRP,使用α-溴苯乙酸乙酯作为具有高引发剂效率的典型引发剂。聚合动力学研究、多次可控的“开-关”光切换循环调节和链延伸实验证实了这种有前景的光诱导无金属ATRP体系在ppm级光催化剂4CzIPN存在下具有良好的分子量控制的“活性”/可控特性。