Triphenylphosphine Photorelease and Induction of Catalytic Activity from Ruthenium-Arene Complexes Bearing a Photoswitchable o-Tosylamide Azobenzene Ligand
被引:11
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Deo, Claire
[1
]
Bogliotti, Nicolas
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Univ Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, FranceUniv Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, France
Bogliotti, Nicolas
[1
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Retailleau, Pascal
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Univ Paris Saclay, Univ Paris 11, Inst Chim Subst Nat, CNRS,UPR 2301, 1 Ave Terrasse, F-91198 Gif Sur Yvette, FranceUniv Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, France
Retailleau, Pascal
[2
]
Xie, Juan
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Univ Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, FranceUniv Paris Saclay, CNRS, ENS Cachan, PPSM, F-94235 Cachan, France
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
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.