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水氧化是光解水制氢气的瓶颈反应,认识和理解水氧化机制并研发廉价稳定的催化剂对解决这一问题尤为重要.自1982年Meyer课题组报道了第一例分子型双核钌水氧化催化剂(blue dimer)以来,过渡金属配合物被广泛应用于探索这一氧化过程的规律和机理,特别是近几年廉价金属配合物在水氧化领域的应用也备受关注.由于水氧化一般在苛刻的氧化条件下才可以实现,如何提高过渡金属配合物在催化条件下的稳定性一直是分子催化剂结构设计的一个难点.利用部分分子催化剂的不稳定性,将其作为前体制备非均相金属氧化物催化剂,广泛用于水氧化研究.然而,对于催化水氧化过程中造成分子催化剂不稳定的因素却鲜有探讨.因此,了解分子催化剂和异相活性物种之间原位转化的机理对于分子催化剂设计至关重要.本文考察了大环配体(TAML)的三价铜配合物(TAML-CuⅢ)的氧化还原性质及其电催化水氧化的反应性能.实验结果表明,TAML-CuⅢ的催化水氧化活性与缓冲溶液种类有关,在磷酸盐溶液与碳酸氢钠溶液中均无催化活性,而在硼酸溶液中表现出较高的催化活性.此外,TAML-CuⅢ具有与本课题组之前报道的TAML-CoⅢ截然不同的电化学行为.TAML-CuⅢ只能发生配体的单电子氧化生成TAML?+-CuⅢ,且该物种无法实现对水分子的活化.进一步实验结果表明,生成的TAML?+-CuⅢ在硼酸根的协助下可以发生进一步氧化和配体的水解,从而生成具有高活性的非均相物种.研究表明该活性物种为含硼的氧化铜物种(B/CuOx).通过本文研究可得出两个结论:(1)具有平面四方构型的三价铜配合物不是一种有效催化水氧化的分子型催化剂;(2)缓冲阴离子在分子催化剂的分解中起到了关键作用.因此,缓冲溶液的选择对催化剂的电化学行为以及稳定性有着重要的影响.“,”Water oxidation is the bottleneck of artificial photosynthesis. Since the first ruthenium-based mo-lecular water oxidation catalyst, the blue dimer, was reported by Meyer's group in 1982, catalysts based on transition metals have been widely employed to explore the mechanism of water oxida-tion. Because the oxidation of water requires harsh oxidative conditions, the stability of transition complexes under the relevant catalytic conditions has always been a challenge. In this work, we report the redox properties of a Cu Ⅲ complex (TAML-Cu Ⅲ) with a redox-active macrocyclic ligand (TAML) and its reactivity toward catalytic water oxidation. TAML-Cu Ⅲ displayed a completely dif-ferent electrochemical behavior from that of the TAML-Co Ⅲ complex previously reported by our group. TAML-Cu Ⅲ can only be oxidized by one-electron oxidation of the ligand to form TAML?+-Cu Ⅲ and cannot achieve water activation through the ligand-centered proton-coupled electron transfer that takes place in the case of TAML-Co Ⅲ. The generated TAML?+-Cu Ⅲ intermediate can undergo further oxidation and ligand hydrolysis with the assistance of borate anions, triggering the for-mation of a heterogeneous B/CuOx nanocatalyst. Therefore, the choice of the buffer solution has a significant influence on the electrochemical behavior and stability of molecular water oxidation catalysts.