Results 221 to 230 of about 16,148 (267)
Some of the next articles are maybe not open access.
The Catalytic Dehydrocoupling of Amine–Boranes and Phosphine–Boranes
2015Mechanistic studies into the catalysed dehydrocoupling of amine–boranes and phosphine–boranes have seen a rapid development over the last 5 years. The primary driver for this intense research effort has been the development of catalysts that might offer significant benefits with regard to the kinetics of hydrogen release, for potential use when linked ...
Heather C. Johnson +2 more
openaire +1 more source
Comparative Toxicity of Boranes
American Industrial Hygiene Association Quarterly, 1955Abstract The acute toxicity of dimethyl-amine-borane, together with the acute toxicity of pyridine-borane and tri-methylamine-borane, are reported. On a weight basis, the order of toxicity was found to be dimethyla-mine-pyridine-trimethylamine-borane. However, when expressed in terms of mgB/kg, the LD50 values form two distinct groups. Recalculation of
openaire +2 more sources
Energy Environ. Sci., 2014
Slurries of ammonia-borane and functionalized amine-boranes form liquid spent fuels after heating in batch or flow-thru reactors.
Asa E. Carre-Burritt +4 more
openaire +1 more source
Slurries of ammonia-borane and functionalized amine-boranes form liquid spent fuels after heating in batch or flow-thru reactors.
Asa E. Carre-Burritt +4 more
openaire +1 more source
Ammonia–Borane and Amine–Borane Dehydrogenation Mediated by Complex Metal Hydrides
Chemical Reviews, 2016This review is a comprehensive survey of the last 10 years of research on ammonia-borane and amine-borane dehydrogenation mediated by complex metal hydrides (CMHs), within the broader context of chemical hydrogen storage. The review also collects those cases where CMHs are the catalyst spent form or its resting state.
Rossin Andrea, Peruzzini Maurizio
openaire +3 more sources
ChemInform Abstract: DIMETHYLSULFID‐BORAN ALS BORAN‐TRAEGER
Chemischer Informationsdienst. Organische Chemie, 1971AbstractDas Boran‐Addukt (III) wird direkt aus dem Sulfid (I) und Diboran (II) bei 0°C dargestellt.
JOHN BERES +3 more
openaire +1 more source
Mild reduction of chlorophosphine boranes to secondary phosphine boranes
Tetrahedron Letters, 2003A number of reducing reagents were assessed in the transformation of chlorophosphine boranes to secondary phosphine boranes. The efficiency of the process requires judicious matching between steric and electronic requirements of reductant and the substrate. The stereochemistry of the reduction was investigated by using a chiral precursor.
Hubert Lam +2 more
openaire +1 more source
Journal of the Less Common Metals, 1981
Abstract Structural comparisons between the higher borides and the boranes, carboranes and metallo derivatives suggest that there may be new borane structures. Also, if lower temperature, very high pressure synthetic conditions are tried, we may find three-dimensional boride-like structures containing other polyhedra and their fragments, particularly
openaire +1 more source
Abstract Structural comparisons between the higher borides and the boranes, carboranes and metallo derivatives suggest that there may be new borane structures. Also, if lower temperature, very high pressure synthetic conditions are tried, we may find three-dimensional boride-like structures containing other polyhedra and their fragments, particularly
openaire +1 more source
Chemistry of boranes. XXII. The acidity of boranes
Collection of Czechoslovak Chemical Communications, 1971S. Heřmánek, H. Plotová
openaire +1 more source
Dimethyl sulfide-borane as a borane carrier
Inorganic Chemistry, 1971Roy M. Adams +3 more
openaire +1 more source