Kistner Lucas, Sigmund Lukas Maximilian, Grieser Fabian Frank, Krauß Julian, Leingang Simone, Kaifer Elisabeth, Greb Lutz, Himmel Hans-Jörg
Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.
Angew Chem Int Ed Engl. 2024 Jan 22;63(4):e202317462. doi: 10.1002/anie.202317462. Epub 2023 Dec 20.
The selective formation of homonuclear bonds is of key importance in synthetic chemistry. Especially, dehydrocoupling reactions are attractive as ecologically and economically friendly alternatives to established reductive bond forming reactions, since they do not require the use of stoichiometric amounts of a reducing reagent and produce only valuable dihydrogen as by-product. Here, we report on a metal-free B-B dehydrocoupling reaction that starts directly from a simple, easily accessible BH adduct, providing convenient access to a new nucleophilic dihydridodiborane in excellent yield. The dihydridodiborane in turn activates dihydrogen, allowing to obtain quantitatively the dideuteridodiborane from the dihydridodiborane by D activation. On the basis of detailed quantum-chemical calculations, the mechanism of this unprecedented reaction is elucidated. Some key points that are essential for metal-free dehydrocoupling are disclosed, paving the way for their systematic evaluation and application.
同核键的选择性形成在合成化学中至关重要。特别是,脱氢偶联反应作为既定还原键形成反应的生态和经济友好型替代方法具有吸引力,因为它们不需要使用化学计量的还原试剂,并且仅产生有价值的副产物氢气。在此,我们报道了一种无金属的B-B脱氢偶联反应,该反应直接从一种简单、易于获得的BH加合物开始,以优异的产率方便地获得一种新的亲核二氢二硼烷。二氢二硼烷进而激活氢气,使得通过D活化从二氢二硼烷定量获得二氘二硼烷。基于详细的量子化学计算,阐明了这一前所未有的反应机理。揭示了无金属脱氢偶联的一些关键要点,为其系统评估和应用铺平了道路。