Department of Chemistry C, University of Zurich, Winterthurerstrasse 190, 8057, Zürich, Switzerland.
ChemSusChem. 2017 Nov 23;10(22):4561-4569. doi: 10.1002/cssc.201701527. Epub 2017 Oct 24.
Bio-mimetic catalysts such as LnCo (OR) (Ln=Er, Tm; OR=alkoxide) cubanes have recently been in the focus of research for artificial water oxidation processes. Previously, the remarkable adaptability with respect to ligand shell, nuclear structure as well as protonation and oxidation states of those catalysts has been shown to be beneficial for the water oxidation process. We further explored the structural flexibility of those catalysts and present here a series of novel structures in which one metal center is pulled out of the cubane cage. This leads to an open cubane core, which is to some extent reminiscent of observed open/closed cubane-core forms of the oxygen-evolving complex in nature's photosystem II. We investigate how those open cubane core models alter the thermodynamics of the water oxidation cycle and how different solvation approaches influence their stability.
仿生催化剂如 LnCo(OR)(Ln=Er,Tm;OR=烷氧基)立方烷最近成为人工水氧化过程的研究焦点。此前,这些催化剂在配体壳、核结构以及质子化和氧化态方面的显著适应性已被证明有利于水氧化过程。我们进一步探索了这些催化剂的结构灵活性,并在此展示了一系列新型结构,其中一个金属中心被拉出立方烷笼。这导致了一个开放的立方烷核心,在某种程度上让人联想到自然界光合作用系统 II 中观察到的开放/闭合立方烷核心形式的氧释放复合物。我们研究了这些开放立方烷核心模型如何改变水氧化循环的热力学,以及不同的溶剂化方法如何影响它们的稳定性。