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Attempts to synthesize solvent-free MgB12H12 by heating various solvated forms (H2O, NH3, and CH3OH) of the salt failed because of the competition between desolvation and dehydrogenation. This competition has been studied by thermogravimetric analysis (TGA) and temperature-programmed desorption (TPD). Products were characterized by IR, solution- and solid-state NMR spectroscopy, elemental analysis, and single-crystal or powder X-ray diffraction analysis. For hydrated salts, thermal decomposition proceeded in three stages, loss of water to form first hexahydrated then trihydrated, and finally loss of water and hydrogen to form polyhydroxylated complexes. For partially ammoniated salts, two stages of thermal decomposition were observed as ammonia and hydrogen were released with weight loss first of 14 % and then 5.5 %. Thermal decomposition of methanolated salts proceeded through a single step with a total weight loss of 32 % with the release of methanol, methane, and hydrogen. All the gaseous products of thermal decomposition were characterized by using mass spectrometry. Residual solid materials were characterized by solid-state 11B magic -angle spinning (MAS) NMR spectroscopy and X-ray powder diffraction analysis by which the molecular structures of hexahydrated and trihydrated complexes were solved. Both hydrogen and dihydrogen bonds were observed in structures of [Mg(H2O)6B12H12] ⋅6 H2O and [Mg(CH3OH)6B12H12] ⋅6 CH3OH, which were determined by single-crystal X-ray diffraction analysis. The structural factors influencing thermal decomposition behavior are identified and discussed. The dependence of dehydrogenation on the formation of dihydrogen bonds may be an important consideration in the design of solid-state hydrogen storage materials. [ABSTRACT FROM AUTHOR]

Ammonia borane (AB) is the most widely studied hydride for hydrogen storage in addition to being a useful reducing agent. Attempts to synthesize pure AB through simple displacement reactions date back to the 1960s; but have been thwarted by the formation of the diammoniate of diborane (DADB), an ionic byproduct. Based on our recent characterization of the formation mechanism of DADB, we have developed a large-scale synthesis of pure AB by both increasing the basicity of the Lewis base of the borane carrier and using a nonpolar solvent to limit the formation of an intermediate, the ammonia diborane (AaDB). Conditions were optimized for the preparation of pure AB by two displacement reactions, either ammonia with dimethylsulfide borane or ammonia with dimethylaniline borane in toluene at room temperature. These procedures are also suitable for preparation of other amine boranes which had the same problem of forming ionic byproducts during displacement reactions. [ABSTRACT FROM AUTHOR]

The article discusses a study which reported the sulfur-free synthesis of the dihydrogen-bonded compound (NH4)2B10H101.5H2O (I), and its anhydrous analog (NH4)2B10H10. The research has identified the compound's anhydrous analog (NH4)2B10H10 and their characterization by NMR, IR, single-crystal X-ray diffraction analysis.

The structure of the title compound, [Mg(AlH(4))(2)(C(4)H(8)O)(4)], has been redetermined at 150 K. The Mg(II) ion is hexa-coordinated to four tetra-hydro-furan (THF) ligands, and two AlH(4) (-) anions through bridging H atoms. The Al-H distances are more precise compared to those previously determined [Nöth et al. (1995 ▶). Chem. Ber. 128, 999-1006; Fichtner & Fuhr (2002 ▶). J. Alloys Compd, 345, 386-396]. The mol-ecule has twofold rotation symmetry.