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・ Diphenylsilanediol
・ Diphenylzinc
・ Diphepanol
・ Diphete Bopape
・ Diphetor
・ Diphilus
・ Diphilus (physician)
・ Diphlebia
・ Diphlebia coerulescens
・ Diphlebia euphoeoides
・ Diphlebiidae
・ Diphlorethol
・ Diphone
・ Diphoorn
・ Diphosgene
Diphosphane
・ Diphosphate-purine nucleoside kinase
・ Diphosphate—glycerol phosphotransferase
・ Diphosphate—serine phosphotransferase
・ Diphosphene
・ Diphosphenes
・ Diphosphines
・ Diphosphoglycerate
・ Diphosphoglyceric acid
・ Diphosphoinositol-pentakisphosphate kinase
・ Diphosphoinositol-polyphosphate diphosphatase
・ Diphosphomevalonate decarboxylase
・ Diphosphorus
・ Diphosphorus tetraiodide
・ Diphosphorus tetroxide


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Diphosphane : ウィキペディア英語版
Diphosphane

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Diphosphane is an inorganic compound with the chemical formula P2H4. This colourless liquid is one of several binary phosphorus hydrides. It is the impurity that typically causes samples of phosphine to ignite in air. An older name is ''diphosphine''.
==Properties, preparation, reactions==
Diphosphane adopts the gauche conformation (like hydrazine, less symmetrical than shown in the image) with a P-P distance of 2.219 angstroms. It is nonbasic, unstable at room temperature, and spontaneously flammable in air. It is only poorly soluble in water but dissolves in organic solvents. Its 1H NMR spectrum consists of 32 lines resulting from an A2XX'A'2 splitting system.
Diphosphane is produced by the hydrolysis of calcium monophosphide, which can be described as the Ca2+ derivative of P24−. According to an optimized procedure, hydrolysis of 400 g of CaP at -30 °C gives about 20 g of product, slightly contaminated with phosphine.
Reaction of diphosphine with butyllithium affords a variety of condensed polyphosphine compounds.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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