Journal of the Chemical Society, Part 3, Pages 2489-3512The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 2615
Chemical Society (Great Britain). green oxo - pyridine compound was an intermediate in this reaction . This was confirmed by treating a suspension of trans - ReOCl 。( PPh3 ) 2 , in benzene , with wet pyridine ( 2 moles per g . - atom Re ) ...
Chemical Society (Great Britain). green oxo - pyridine compound was an intermediate in this reaction . This was confirmed by treating a suspension of trans - ReOCl 。( PPh3 ) 2 , in benzene , with wet pyridine ( 2 moles per g . - atom Re ) ...
Page 2616
... ( pyridine ) dirhenium ( v ) .- Method A. Pyridine ( 15 ml ) was added to a solution of rhenium pentachloride ( 2 · 0 g . ) in acetone ( reagent grade ; 30 ml . ) . The precipitate was collected , dissolved in dichloromethane , and ...
... ( pyridine ) dirhenium ( v ) .- Method A. Pyridine ( 15 ml ) was added to a solution of rhenium pentachloride ( 2 · 0 g . ) in acetone ( reagent grade ; 30 ml . ) . The precipitate was collected , dissolved in dichloromethane , and ...
Page 3454
... Pyridine Complexes . By P. MOORE and R. G. WILKINS . The rates of dissociation , in excess of acid , of nickel ( 11 ) mono - complexes with a series of 3- and 4 - monosubstituted pyridines have been investigated spectrally by the ...
... Pyridine Complexes . By P. MOORE and R. G. WILKINS . The rates of dissociation , in excess of acid , of nickel ( 11 ) mono - complexes with a series of 3- and 4 - monosubstituted pyridines have been investigated spectrally by the ...
Contents
Fluorocarbohydrates Part VIII Formation of halogenoderivatives from | 2493 |
Steric influences in radical reactions Part I Benzyl radicals derived from cyclic | 2500 |
56dioisopropylidene | 2514 |
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absorption acetic acid acetone added adduct alcohol Amax Amer aqueous aromatic ation atom atomic orbitals band benzene bond bromide Calc carbon carbonyl CH₂ Chem chloroform chromatography cm.¹ complex compound concentrated cooled crystallised cyclic cyclohexane decomp decomposition dilute dioxide distilled dried electron elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate formation formed Found fraction gave give heated hydrochloric hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum ionisation energies isolated isomer ketone kinetic light petroleum mechanism methyl mixed m. p. mixture mole molecular molecule nitrate nitric nitric oxide nitrogen Nujol obtained oxide oxime perchlorate petroleum b. p. polymer potassium potassium hydroxide prepared proton pyridine reaction rearrangement reduced refluxed requires residue room temperature salt sodium solid solution solvent spectra structure sulphuric acid Table thionyl chloride transition ultraviolet values Vmax yellow yield