化学
铱
光催化
化学计量学
联轴节(管道)
光化学
反应机理
激发态
金属有机化学
偶联反应
动能
镍
反应速率
物理化学
催化作用
有机化学
冶金
原子物理学
材料科学
物理
量子力学
作者
Nicholas A. Till,Lei Tian,Zhe Dong,Gregory D. Scholes,David W. C. MacMillan
摘要
The combined use of reaction kinetic analysis, ultrafast spectroscopy, and stoichiometric organometallic studies has enabled the elucidation of the mechanistic underpinnings to a photocatalytic C-N cross-coupling reaction. Steady-state and ultrafast spectroscopic techniques were used to track the excited-state evolution of the employed iridium photocatalyst, determine the resting states of both iridium and nickel catalysts, and uncover the photochemical mechanism for reductive activation of the nickel cocatalyst. Stoichiometric organometallic studies along with a comprehensive kinetic study of the reaction, including rate-driving force analysis, unveiled the crucial role of photocatalysis in both initiating and sustaining a Ni(I)/Ni(III) cross-coupling mechanism. The insights gleaned from this study further enabled the discovery of a new photocatalyst providing a >30-fold rate increase.
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