Molecular early main group metal hydrides: synthetic challenge, structures and applications

被引:122
作者
Harder, Sjoerd [1 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, NL-9749 AG Groningen, Netherlands
关键词
HYDROGEN-STORAGE MATERIALS; SOLUBLE CALCIUM HYDRIDE; THERMAL-DECOMPOSITION; MAGNESIUM HYDRIDE; MESO-OCTAETHYLPORPHYRINOGEN; STEREOSELECTIVE REDUCTION; BERYLLIUM HYDRIDES; BICYCLIC KETONES; PYRIDINE ADDUCT; COMPLEXES;
D O I
10.1039/c2cc33478j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Within the general area of early main group metal chemistry, the controlled synthesis of well-defined metal hydride complexes is a rapidly developing research field. As group 1 and 2 metal complexes are generally highly dynamic and lattice energies for their [MH](infinity) and [MH2](infinity) salts are high, the synthesis of well-defined soluble hydride complexes is an obvious challenge. Access to molecular early main group metal hydrides, however, is rewarding: these hydrocarbon-soluble metal hydrides are highly reactive, have found use in early main group metal catalysis and are potentially also valuable molecular model systems for polar metal hydrides as a hydrogen storage material. The article focusses specifically on alkali and alkaline-earth metal hydride complexes and discusses the synthetic challenge, molecular structures, reactivity and applications.
引用
收藏
页码:11165 / 11177
页数:13
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