Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Weixian Xi"'
Autor:
Weixian Xi, Xinpeng Zhang, Guangzhe Gao, Christopher N. Bowman, Xiance Wang, Jeffrey W. Stansbury
Publikováno v:
ACS Macro Letters. 7:852-857
In this contribution, three o-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 (
Publikováno v:
ACS Macro Letters. 5:229-233
An efficient visible-light-sensitive photobase generator for thiol-Michael addition reactions was synthesized and evaluated. This highly reactive catalyst was designed by protecting a strong base (tetramethyl guanidine, TMG) with a visible-light-resp
Autor:
J.W. Stansbury, Alan Aguirre-Soto, Haiyan Peng, Christopher N. Bowman, Weixian Xi, Christopher J. Kloxin
Publikováno v:
Macromolecules
Photochemical processes enable spatial and temporal control of reactions, which can be implemented as an accurate external control approach in both polymer synthesis and materials applications. "Click" reactions have also been employed as efficient t
Autor:
Tao Gong, Shunsuke Chatani, Weixian Xi, Maciej Podgórski, Christopher N. Bowman, Devatha P. Nair, Christopher R. Fenoli
Publikováno v:
Chemistry of Materials. 26:724-744
The key attribute of the thiol-Michael addition reaction that makes it a prized tool in materials science is its modular “click” nature, which allows for the implementation of this highly efficient, “green” reaction in applications that vary
Autor:
Devatha P. Nair, Tao Gong, Shunsuke Chatani, Maciej Podgórski, Christopher R. Fenoli, Weixian Xi, Christopher N. Bowman
Publikováno v:
ChemInform. 45
The key attribute of the thiol-Michael addition reaction that makes it a prized tool in materials science is its modular “click” nature, which allows for the implementation of this highly efficient, “green” reaction in applications that vary
Publikováno v:
ChemInform. 44
The utilization of 2-(2-nitrophenyl)propyloxycarbonyl as a photolabile primary amine cage enables the thiol-Michael ′click′ reaction to be photo-triggered.
Publikováno v:
Chemical communications (Cambridge, England). 49(40)
The utilization of 2-(2-nitrophenyl)propyloxycarbonyl (NPPOC) as a photolabile primary amine cage enables the thiol-Michael 'click' reaction to be photo-triggered. The photolabile amine exhibits efficient catalytic activity upon UV irradiation and is