Journal of the Chemical Society, Part 5The Society., 1965 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 74
Page 6291
... hydrogen atoms . It was found impossible to prepare compounds of the type K + [ X , PBY ] ( where X and Y = H or Me ) ... hydrogen was rapidly produced . Further heating to 300 ° succeeded in re- moving only another mol . of hydrogen ...
... hydrogen atoms . It was found impossible to prepare compounds of the type K + [ X , PBY ] ( where X and Y = H or Me ) ... hydrogen was rapidly produced . Further heating to 300 ° succeeded in re- moving only another mol . of hydrogen ...
Page 6295
... hydrogen ( 3.34 mmoles ) , and phosphine ( 0.49 mmole ) as volatile products . The solution contained potassium ions ( 0.59 milliatom ) and an indeterminable amount of boric acid , the determination being hindered because of the ...
... hydrogen ( 3.34 mmoles ) , and phosphine ( 0.49 mmole ) as volatile products . The solution contained potassium ions ( 0.59 milliatom ) and an indeterminable amount of boric acid , the determination being hindered because of the ...
Page 7397
... hydrogen stretching mode . Generally monohydrides [ IrHX , L ] of configuration ( I ) have much lower iridium - hydrogen stretching frequencies ( 2000-2100 cm . - 1 ) than the corresponding isomers of configuration ( II ) ( 2195-2220 cm ...
... hydrogen stretching mode . Generally monohydrides [ IrHX , L ] of configuration ( I ) have much lower iridium - hydrogen stretching frequencies ( 2000-2100 cm . - 1 ) than the corresponding isomers of configuration ( II ) ( 2195-2220 cm ...
Contents
6613 | 5783 |
Transitionmetal quinoxaline complexes Part II Copper1 derivatives | 5784 |
ptolyl | 5785 |
180 other sections not shown
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Common terms and phrases
absorption acetic acid acetic anhydride acetone Amer amine anhydride aqueous atoms band benzene benzyl bond borazocine boron bromide Calc carbon carbon tetrachloride CH₂ Chem chloride chloroform chromatography cm.¹ colourless complex compounds concentration crystallised decomp derivatives dibromide dilute dissolved distilled elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate fluoride Found fraction gave give heated under reflux hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum isolated isomer ketone ligand light petroleum m. p. and mixed methyl mixed m. p. mixture mmoles mole molecule n.m.r. spectrum nitrogen obtained olefin optical oxazolone oxide peak perchlorate phenyl potassium prepared protons pyridine Raney nickel reaction requires residue ring room temperature salt showed sodium sodium hydroxide solid solution solvent spectra structure sulphide sulphoxide sulphuric Table thionyl chloride vacuo values VIII yellow yield