Institute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, 52056, Aachen, Germany.
Angew Chem Int Ed Engl. 2018 Feb 5;57(6):1458-1473. doi: 10.1002/anie.201708592. Epub 2017 Dec 14.
Solid magnesium hydride [MgH ] has been pursued as a potential hydrogen-storage material. Organic chemists were rather interested in soluble magnesium hydride reagents from mid-20th century. It was only in the last two decades that molecular magnesium hydride chemistry received a major boost from organometallic chemists with a series of structurally well-characterized examples that continues to build a whole new class of compounds. More than 40 such species have been isolated, ranging from mononuclear terminal hydrides to large hydride clusters with more than 10 magnesium atoms. They provide not only insights into the structure and bonding of Mg-H motifs, but also serve as models for hydrogen-storage materials. Some of them are also recognized to participate in catalytic transformations, such as hydroelementation. Herein, an overview of these molecular magnesium hydrides is given, focusing on their synthesis and structural characterization.
固体氢化镁[MgH ]一直被视为一种有潜力的储氢材料。20 世纪中叶以来,有机化学家对可溶解的氢化镁试剂产生了浓厚的兴趣。直到过去二十年,一系列结构得到很好表征的有机金属镁氢化化合物的出现,才使得分子镁氢化化学得到了有机化学家们的重视,这些化合物也不断构建出一个全新的化合物类别。目前已经分离出 40 多种这样的物质,从单核端氢化物到含有 10 个以上镁原子的大型氢化物簇都有。它们不仅为 Mg-H 键合模式的结构和键合提供了深入的了解,还可以作为储氢材料的模型。其中一些还被认为可以参与催化转化,如氢化反应。本文主要介绍了这些分子镁氢化合物的合成和结构特征。