Triphenylphosphine Photorelease and Induction of Catalytic Activity from Ruthenium-Arene Complexes Bearing a Photoswitchable o-Tosylamide Azobenzene Ligand

被引:11
作者
Deo, Claire [1 ]
Bogliotti, Nicolas [1 ]
Retailleau, Pascal [2 ]
Xie, Juan [1 ]
机构
[1] Univ Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, France
[2] Univ Paris Saclay, Univ Paris 11, Inst Chim Subst Nat, CNRS,UPR 2301, 1 Ave Terrasse, F-91198 Gif Sur Yvette, France
关键词
BAYLIS-HILLMAN REACTION; SODIUM-BOROHYDRIDE; BENZENE LIGAND; DNA-BINDING; PHOTOACTIVATION; EFFICIENT; BIOMOLECULES; HYDROLYSIS; CHEMISTRY; BEHAVIOR;
D O I
10.1021/acs.organomet.6b00431
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactivity of cationic arene ruthenium complexes bearing a photoswitchable o-tosylamide azobenzene ligand toward various phosphorus nucleophiles was investigated. The resulting phosphine-ruthenium complexes containing an azobenzene ligand were isolated as the Z isomer. Under appropriate reaction conditions, quantitative triphenylphosphine photorelease from the complex was achieved through Z -> E isomerization of the ligand. This process was applied to the photoinitiation of the catalytic aza-Morita-Baylis-Hillman reaction.
引用
收藏
页码:2694 / 2700
页数:7
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