Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1124
... Equilibrium constants were calculated from which theoretical equilibrium concentrations corres- ponding to these constants were computed . Six different species are present at equilibrium in systems ( i ) and ( ii ) and ten species in ...
... Equilibrium constants were calculated from which theoretical equilibrium concentrations corres- ponding to these constants were computed . Six different species are present at equilibrium in systems ( i ) and ( ii ) and ten species in ...
Page 1125
... equilibrium are listed in the Tables . 9 Weighted average values of the equilibrium constants and their standard errors were calculated using previously established computer programs for the IBM 7044 computer . In addition , a new ...
... equilibrium are listed in the Tables . 9 Weighted average values of the equilibrium constants and their standard errors were calculated using previously established computer programs for the IBM 7044 computer . In addition , a new ...
Page 1856
... equilibrium ( 4 ) are very close or that the order of magnitude of the separate relaxation times are so different that only one is active in the present fre- quency range . According to the i.r. evidence only the two isomers ( IV ) and ...
... equilibrium ( 4 ) are very close or that the order of magnitude of the separate relaxation times are so different that only one is active in the present fre- quency range . According to the i.r. evidence only the two isomers ( IV ) and ...
Contents
Dolcetti G See Peloso A 1506 | 1031 |
Structures of cyclic amides Part III Thio and selenolactams | 1033 |
Equilibria in solutions which contain a metal ion and an aminoacid | 1039 |
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¹H n.m.r. spectrum absorption acetaldehyde acetone acid adduct Amer anion aqueous atoms bands benzene bond bromine trifluoride calculated carbon catalyst cation Chem chemical Chemistry chloride cm.¹ co-ordination cobalt(II coefficients complexes compounds concentration configuration corresponding coupling constant crystals cyanide dehy gel dichloromethane dilute doublet electronic energy equation ethanol ether experimental Figure five-co-ordinate fluorine formation frequencies halide heat hydrogen hydrogen cyanide hydrolysis i.r. spectra Inorg iodide iodobenzene isomers k₁ kcal lactams ligand magnetic Mc./sec measured metal methyl mixture mmoles mole-¹ molecular molecule n.m.r. spectra nickel nickel(II nitric oxide nitrogen observed obtained octahedral orbital oxygen parameters phosphine phosphorus Phys plexes PMe,Ph potassium prepared present proton Raman reaction resonance room temperature sample scandium(III showed shown similar sodium solid solution solvent species structure sulphur Table thallium thio thiocyanate thiocyanogen thiolactams titration trans trimethylsilyl tris(trimethylsilyl values yellow