Pan Xiangcheng, Malhotra Nikhil, Dadashi-Silab Sajjad, Matyjaszewski Krzysztof
Center for Macromolecular Engineering, Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA, 15213, USA.
Macromol Rapid Commun. 2017 Jul;38(13). doi: 10.1002/marc.201600651. Epub 2016 Dec 20.
A photoinduced atom transfer radical polymerization (photoATRP) of methacrylates is investigated using air-stable FeBr as catalyst in the absence of conventional ATRP initiators, additional ligands, reducing agents, and/or radical initiators. The ATRP alkyl halide initiator is formed in situ via photoreduction of FeBr by methacrylate monomers. The kinetics of the polymerization display a linear semilogarithmic plot after several hours of induction period. The molecular weight can be modulated by additions of different amounts of FeBr , and polymers have narrow molecular weight distributions. Thus, FeBr acts as deactivator, as well as a source of activator FeBr and initiator. This method features a temporal control, and can provide various polymethacrylates with high chain end functionality.
在不存在传统原子转移自由基聚合(ATRP)引发剂、额外配体、还原剂和/或自由基引发剂的情况下,使用空气稳定的FeBr作为催化剂研究了甲基丙烯酸酯的光诱导原子转移自由基聚合(photoATRP)。ATRP卤代烷引发剂通过甲基丙烯酸酯单体对FeBr的光还原原位形成。聚合动力学在诱导期数小时后呈现线性半对数图。分子量可通过添加不同量的FeBr进行调节,聚合物具有窄的分子量分布。因此,FeBr既作为失活剂,又作为活化剂FeBr和引发剂的来源。该方法具有时间控制功能,可提供具有高链端官能度的各种聚甲基丙烯酸酯。