Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1212
... values were combined with pK values to calculate AS values . pk Values were obtained from the literature for 51 compounds and new values were determined for 18 compounds . A compilation of pK , AH3 , and AS values from the present study ...
... values were combined with pK values to calculate AS values . pk Values were obtained from the literature for 51 compounds and new values were determined for 18 compounds . A compilation of pK , AH3 , and AS values from the present study ...
Page 1221
... values for proton ionization from the saturated or unsubstituted ( methyl group in place of substituent group ) molecule and those for the unsaturated or substituted molecule . Values of AX ° diff are given in Table 4. Wherever possible ...
... values for proton ionization from the saturated or unsubstituted ( methyl group in place of substituent group ) molecule and those for the unsaturated or substituted molecule . Values of AX ° diff are given in Table 4. Wherever possible ...
Page 1347
... values . The average value of K , was calculated and the procedure was reversed to obtain values of [ H + ] and hence kcale from this average acidity constant and the same values of B ; and p . A suitable computer programme was used for ...
... values . The average value of K , was calculated and the procedure was reversed to obtain values of [ H + ] and hence kcale from this average acidity constant and the same values of B ; and p . A suitable computer programme was used for ...
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