Universität Würzburg, Institut für Organische Chemie and Center for Nanosystems Chemistry, Am Hubland, 97074 Würzburg, Germany.
Nat Chem. 2016 Jun;8(6):576-83. doi: 10.1038/nchem.2503. Epub 2016 May 2.
Mimicking the ingenuity of nature and exploiting the billions of years over which natural selection has developed numerous effective biochemical conversions is one of the most successful strategies in a chemist's toolbox. However, an inability to replicate the elegance and efficiency of the oxygen-evolving complex of photosystem II (OEC-PSII) in its oxidation of water into O2 is a significant bottleneck in the development of a closed-loop sustainable energy cycle. Here, we present an artificial metallosupramolecular macrocycle that gathers three Ru(bda) centres (bda = 2,2'-bipyridine-6,6'-dicarboxylic acid) that catalyses water oxidation. The macrocyclic architecture accelerates the rate of water oxidation via a water nucleophilic attack mechanism, similar to the mechanism exhibited by OEC-PSII, and reaches remarkable catalytic turnover frequencies >100 s(-1). Photo-driven water oxidation yields outstanding activity, even in the nM concentration regime, with a turnover number of >1,255 and turnover frequency of >13.1 s(-1).
模仿大自然的巧妙设计,并利用自然选择在数十亿年中发展出的无数种有效的生化转化,是化学家工具箱中最成功的策略之一。然而,在将水氧化为氧气的过程中,我们无法复制光合作用系统 II (OEC-PSII)中氧气产生复合物的优雅和高效,这是开发闭环可持续能源循环的一个重大瓶颈。在这里,我们展示了一种人工金属超分子大环,它聚集了三个 Ru(bda)中心(bda=2,2'-联吡啶-6,6'-二羧酸),可催化水氧化。大环的结构通过亲核水攻击机制加速水氧化速率,类似于 OEC-PSII 所表现出的机制,达到了显著的催化周转率频率 >100 s(-1)。光驱动的水氧化即使在纳摩尔浓度范围内也具有出色的活性,周转数 >1,255,周转率频率 >13.1 s(-1)。