Cagan David A, Bím Daniel, Kazmierczak Nathanael P, Hadt Ryan G
Division of Chemistry and Chemical Engineering, Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, California 91125, United States.
Institute of Organic Chemistry and Biochemistry, The Czech Academy of Sciences, Flemingovo nám. 2, Prague 6 166 10, Czech Republic.
ACS Catal. 2024 May 29;14(11):9055-9076. doi: 10.1021/acscatal.4c02036. eCollection 2024 Jun 7.
Metallaphotoredox catalysis can unlock useful pathways for transforming organic reactants into desirable products, largely due to the conversion of photon energy into chemical potential to drive redox and bond transformation processes. Despite the importance of these processes for cross-coupling reactions and other transformations, their mechanistic details are only superficially understood. In this review, we have provided a detailed summary of various photoredox mechanisms that have been proposed to date for Ni-bipyridine (bpy) complexes, focusing separately on photosensitized and direct excitation reaction processes. By highlighting multiple bond transformation pathways and key findings, we depict how photoredox reaction mechanisms, which ultimately define substrate scope, are themselves defined by the ground- and excited-state geometric and electronic structures of key Ni-based intermediates. We further identify knowledge gaps to motivate future mechanistic studies and the development of synergistic research approaches spanning the physical, organic, and inorganic chemistry communities.
金属光氧化还原催化能够开启将有机反应物转化为理想产物的有用途径,这主要归功于光子能量转化为化学势以驱动氧化还原和键转化过程。尽管这些过程对于交叉偶联反应及其他转化至关重要,但其机理细节仅得到了初步了解。在本综述中,我们详细总结了迄今为止针对镍-联吡啶(bpy)配合物所提出的各种光氧化还原机理,分别聚焦于光敏化和直接激发反应过程。通过突出多种键转化途径和关键发现,我们描述了光氧化还原反应机理(其最终决定了底物范围)是如何由关键镍基中间体的基态和激发态几何结构及电子结构所决定的。我们进一步明确了知识空白,以推动未来的机理研究以及跨越物理、有机和无机化学领域的协同研究方法的发展。