Pressure-induced structural changes in Methylamine borane and dimethylamine borane
نویسندگان
چکیده
منابع مشابه
Axonal polyneuropathy after acute dimethylamine borane intoxication.
OBJECTIVE To study a patient with axonal polyneuropathy due to acute dimethylamine borane (DMAB) intoxication. PATIENT Confusion and drowsiness in the acute stage, followed by cognitive impairments and polyneuropathy, are reported in a chemical factory worker after acute exposure to DMAB. RESULTS Nerve conduction studies indicated axonal polyneuropathy, particularly in the motor nerves. Sur...
متن کاملCase Report: The Clinical Toxicity of Dimethylamine Borane
CONTEXT Dimethylamine borane (DMAB) is a reducing agent used in nonelectric plating of semiconductors. Exposures are usually through occupational contact. We report here four cases of people who suffered from work-related exposure to DMAB. CASE PRESENTATION Three patients exposed to DMAB decontaminated immediately by drinking a lot of water; they reported dizziness, nausea, diarrhea 6-8 hr la...
متن کاملPropylamine–borane
The title compound, C(3)H(12)BN, was solved using data collected from a multiple crystal (note incomplete data shell). The cell packing is dominated by bifurcated attractive N-H(δ+)⋯(δ-)H-B inter-actions.
متن کاملDehydrocoupling of dimethylamine-borane catalysed by rhenium complexes and its application in olefin transfer-hydrogenations.
Re(I) complexes are applied as catalysts for the dehydro-coupling of Me2NH.BH3 and the transfer-hydrogenation of olefins.
متن کاملCatalytic dehydrogenation of dimethylamine borane by group 4 metallocene alkyne complexes and homoleptic amido compounds.
Dehydrogenation of Me(2)NH·BH(3) (1) by group 4 metallocene alkyne complexes of the type Cp(2)M(L)(η(2)-Me(3)SiC(2)SiMe(3)) [Cp = η(5)-cyclopentadienyl; M = Ti, no L (2Ti); M = Zr, L = pyridine (2Zr)] and group 4 metal amido complexes of the type M(NMe(2))(4) [M = Ti (8Ti), Zr (8Zr)] is presented.
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ژورنال
عنوان ژورنال: Journal of Alloys and Compounds
سال: 2017
ISSN: 0925-8388
DOI: 10.1016/j.jallcom.2017.06.174