Zhang Xinpeng, Xi Weixian, Gao Guangzhe, Wang Xiance, Stansbury Jeffrey W, Bowman Christopher N
Department of Chemical and Biological Engineering, University of Colorado Boulder, UCB 596, Boulder, Colorado 80309, United States.
ACS Macro Lett. 2018 Jul 17;7(7):852-857. doi: 10.1021/acsmacrolett.8b00435. Epub 2018 Jun 29.
In this contribution, three -nitrobenzyl-based photobase systems were synthesized and evaluated for visible light initiated thiol-Michael addition polymerizations. With a modified structure, the (3,4-methylenedioxy-6-nitrophenyl)-propyloxycarbonyl (MNPPOC) protected base performance exceeds that of the nonsubstituted 2-(2-nitrophenyl)-propyloxycarbonyl (NPPOC) protected base and an ITX sensitized photobase system, with respect to both long-wavelength light sensitivity and photolytic efficiency. In material synthesis, MNPPOC-TMG is capable of initiating photo thiol-Michael polymerization efficiently and orthogonally with only limited visible light exposure and generating a highly homogeneous cross-linked polymer network. This approach enables the thiol-Michael "click" reaction to be conducted with a low-energy, visible light irradiation and, thus, expands its applications in biocompatible and UV sensitive materials.
在本论文中,合成了三种基于间硝基苄基的光碱体系,并对其在可见光引发的硫醇-迈克尔加成聚合反应中的性能进行了评估。通过结构修饰,(3,4-亚甲二氧基-6-硝基苯基)-丙氧基羰基(MNPPOC)保护的碱在长波长光敏感性和光解效率方面均优于未取代的2-(2-硝基苯基)-丙氧基羰基(NPPOC)保护的碱和ITX敏化的光碱体系。在材料合成中,MNPPOC-TMG仅需有限的可见光照射就能高效且正交地引发光硫醇-迈克尔聚合反应,并生成高度均匀的交联聚合物网络。这种方法使得硫醇-迈克尔“点击”反应能够在低能量可见光照射下进行,从而拓展了其在生物相容性和对紫外线敏感材料中的应用。