Meier Stefan C, Holz Albina, Schmidt Alexei, Kratzert Daniel, Himmel Daniel, Krossing Ingo
Institut für Anorganische und Analytische Chemie, and Freiburger Materialforschungszentrum (FMF), Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
Chemistry. 2017 Oct 17;23(58):14658-14664. doi: 10.1002/chem.201703589. Epub 2017 Sep 18.
The facile synthesis of a pentacarbonyl cobalt(I) salt without the need for a superacid as solvent is presented. This salt, [Co(CO) ] [Al(OR ) ] {R =C(CF ) }, readily accessible on a multigram scale, undergoes substitution reactions with arenes yielding the hitherto unknown class of two-legged cobalt piano-stool complexes [(arene)Co(CO) ] with four different arene ligands. Such a substitution chemistry would have been impossible in superacid solution, as the arenes used would have been oxidized and/or protonated. Thus, the general approach described herein may have a wide synthetic use. Additionally, the thermochemistry of the piano-stool complexes is shown to be not easy to describe computationally and most of the established DFT methods overestimate the reaction energies. Only CCSD(T) calculations close to the basis set limit gave energies fully agreeing with the experiment.
本文介绍了一种无需使用超强酸作为溶剂即可简便合成五羰基钴(I)盐的方法。这种盐[Co(CO)₅][Al(OR)₄](R = C(CF₃)₃)易于以多克规模制备,它与芳烃发生取代反应,生成了迄今未知的一类带有四种不同芳烃配体的双腿钴钢琴凳配合物[(芳烃)Co(CO)₃]。在超强酸溶液中,这样的取代化学是不可能实现的,因为所使用的芳烃会被氧化和/或质子化。因此,本文所述的通用方法可能具有广泛的合成用途。此外,还表明钢琴凳配合物的热化学性质在计算上不易描述,大多数已确立的密度泛函理论(DFT)方法高估了反应能量。只有接近基组极限的耦合簇单双激发(CCSD(T))计算给出的能量与实验完全一致。