Quarterly Journal of the Chemical Society of London, Part 4, Pages 3513-4668 |
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Page 4025
... phosphine and methane , about 50 ± 10 % of the resulting phosphorus - 32 was in the form of phosphine . This retention of [ 32P ] phosphine was not decreased by addition of various rare gases which should act as moderators for hot ...
... phosphine and methane , about 50 ± 10 % of the resulting phosphorus - 32 was in the form of phosphine . This retention of [ 32P ] phosphine was not decreased by addition of various rare gases which should act as moderators for hot ...
Page 4026
... phosphine . Target mixture ( pressures in mm . Hg ) Irradn . Distribution of 32P in products Run time Other Non- Percentage no . ( hr . ) PH , CHA Rare gas PH , volatiles volatiles recovery 94 25 29 59 0.7 40-3 97 27 103 5.5 550 48.6 ...
... phosphine . Target mixture ( pressures in mm . Hg ) Irradn . Distribution of 32P in products Run time Other Non- Percentage no . ( hr . ) PH , CHA Rare gas PH , volatiles volatiles recovery 94 25 29 59 0.7 40-3 97 27 103 5.5 550 48.6 ...
Page 4172
... ( phosphine oxide ) addition compounds . Further oxidation by hydrogen peroxide gives uranyl chloride - bis ( phosphine oxide ) addition compounds . Features of the infrared spectra are reported . Uranium tetrachloride - phosphine and ...
... ( phosphine oxide ) addition compounds . Further oxidation by hydrogen peroxide gives uranyl chloride - bis ( phosphine oxide ) addition compounds . Features of the infrared spectra are reported . Uranium tetrachloride - phosphine and ...
Contents
NO PAGE | 3528 |
The adsorption of stearic acid from solution by oxide adsorbents | 3535 |
The effect of pressure of the electrical conductivity of aqueous mixed electrolyte | 3548 |
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absorption acetic acid acetic anhydride acetone acetyl added alcohol alkaline aluminium Amer amine atoms band benzene benzyl boiling bond bromide Calc carbon cations CH₂ chabazite Chem chloride chloroform chromatography cm.¹ colistin compounds concentration constant crystallised crystals decomp derivatives dilute dimethyl dimethylformamide dioxan dissolved distilled dried ester ethanol ether ethyl acetate evaporated extracted filtrate formation formed Found fraction gave give heated hydrochloric acid hydrochloride hydrogen hydrolysis iodide isomer ketone lithium lithium aluminium hydride m. p. and mixed mixed m. p. mixture mole molecules needles nitrate nitric acid nitrogen o-xylene obtained optical oxide oxygen phenyl phosphine picrate polymyxin potassium precipitate prepared prisms proton pyridine reaction recrystallised reduced refluxed requires residue resonance room temperature salt sodium hydroxide solution solvent spectra stirred structure substitution sulphone sulphuric acid Table tetrahydrofuran values washed yellow yield