Tang Shan, von Wolff Niklas, Diskin-Posner Yael, Leitus Gregory, Ben-David Yehoshoa, Milstein David
J Am Chem Soc. 2019 May 8;141(18):7554-7561. doi: 10.1021/jacs.9b02669. Epub 2019 Apr 30.
Metal-ligand cooperation (MLC) by dearomatization/aromatization provides a unique way for bond activation, which has led to the discovery of various acceptorless dehydrogenative coupling reactions. However, most of the studies are based on pincer complexes with a central nitrogen donor. Aiming at exploration of the possibility of MLC by PCP-type pincer complexes, we report herein the synthesis, characterization, structure, and reactivity of pyridine-based PCP-Ru complexes. X-ray structures and DFT calculations indicate a carbenoid character of quaternized pyridine-based PCP-Ru complexes. These complexes undergo dearomatization by direct deprotonation, and the dearomatized complex can react with hydrogen, alcohols, or nitriles to regain aromatization via MLC.
通过去芳构化/芳构化实现的金属-配体协同作用(MLC)为键活化提供了一种独特的方式,这已导致发现了各种无受体脱氢偶联反应。然而,大多数研究基于具有中心氮供体的钳形配合物。为了探索PCP型钳形配合物实现MLC的可能性,我们在此报告基于吡啶的PCP-Ru配合物的合成、表征、结构和反应性。X射线结构和密度泛函理论计算表明季铵化的基于吡啶的PCP-Ru配合物具有卡宾体特征。这些配合物通过直接去质子化发生去芳构化,而去芳构化的配合物可以与氢气、醇或腈反应,通过MLC重新实现芳构化。