Quarterly Journal of the Chemical Society of London, Part 1, Pages 809-1856 |
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Page 998
... observed infra- red - active stretching frequencies . The presence of only one observed N - O stretching frequency and no stretch- ing frequency assignable to N - N in the infrared suggests that the complexes are based on the trans ...
... observed infra- red - active stretching frequencies . The presence of only one observed N - O stretching frequency and no stretch- ing frequency assignable to N - N in the infrared suggests that the complexes are based on the trans ...
Page 1505
... observed when the 3 - position is substituted . The 0.2 gauss splittings were only observed at low temperatures ( ca. 60 ° ) . Under these conditions the spectrum of the less stable isomer was too weak to be detected . --- Anthraquinone ...
... observed when the 3 - position is substituted . The 0.2 gauss splittings were only observed at low temperatures ( ca. 60 ° ) . Under these conditions the spectrum of the less stable isomer was too weak to be detected . --- Anthraquinone ...
Page 1608
... observed and calculated values of AЕpH , but some divergence in the most concentrated solutions . We have preferred to use the observed values , since these will contain a correction for salt effects not allowed for in the calculations ...
... observed and calculated values of AЕpH , but some divergence in the most concentrated solutions . We have preferred to use the observed values , since these will contain a correction for salt effects not allowed for in the calculations ...
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absorption acetone acid adducts Amer amine anion aqueous assigned bands benzene bond bromide Calc calculated carbon carbonyl cation Chem CHEMISTRY chloride cm.¹ co-ordination cobalt cobalt(II coefficients complexes compounds concentration copper(II crystallised crystals decaborane decomposition derivatives diethyl ether dimer effect electron energy equation ethanol ether EXPERIMENTAL Figure Found frequency function germania groups H₂O halide heated hydration hydrazine hydride hydrogen hydrolysis hydroxide indium indium(III infrared infrared spectra Inorg intensity interactions iodide ionic isomer kcal ligand liquid measured methyl mixture mmole molar mole mole¹ molecular molecules nitrate nitrogen observed obtained octahedral orbital oxide oxygen peaks pentachloride perchlorate phosphorus Phys prepared protactinium proton pyridine rate constants reaction resin room temperature salts similar sodium solid soluble solution solvent solvolysis species spectrum steric structure sulphate symmetry Table tetrahedral tetrahydrofuran thermal trans vacuo values vanadyl ion vibrations X-ray