Quarterly Journal of the Chemical Society of London, Part 4, Pages 3513-4668 |
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Page 4172
... 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 uranium tetrachloride ...
... 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 uranium tetrachloride ...
Page 4174
... addition compounds which form yellow non- hygroscopic crystals . The ease of oxidation appears to increase with the number of phenyl groups . Addition compounds of uranyl chloride , uranyl bromide , and uranyl nitrate with phosphine ...
... addition compounds which form yellow non- hygroscopic crystals . The ease of oxidation appears to increase with the number of phenyl groups . Addition compounds of uranyl chloride , uranyl bromide , and uranyl nitrate with phosphine ...
Page 4180
... addition compounds in which phenyl groups are attached to phosphorus , and the preparation and properties of 2,2,4,4- tetrahalogeno - 1,1,3,3 - tetraphenylcyclodiphosphinoborines , PPh , B2X1 ( X = Br , I ) . 4 4 The molecular addition ...
... addition compounds in which phenyl groups are attached to phosphorus , and the preparation and properties of 2,2,4,4- tetrahalogeno - 1,1,3,3 - tetraphenylcyclodiphosphinoborines , PPh , B2X1 ( X = Br , I ) . 4 4 The molecular addition ...
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