Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1392
... room temperature . As the re- action proceeded the solid dissolved and the solution turned yellow . The solution was taken to small volume and the yellow crystals which separated were washed with dichloro- methane to remove gold complex ...
... room temperature . As the re- action proceeded the solid dissolved and the solution turned yellow . The solution was taken to small volume and the yellow crystals which separated were washed with dichloro- methane to remove gold complex ...
Page 1405
... room temperature . Vigorous evolution of gas was observed on the surface of the rhodium complex . After about 15 min . the starting material had dissolved completely . Bubbling of allene was continued for 1 hr . , then the solution was ...
... room temperature . Vigorous evolution of gas was observed on the surface of the rhodium complex . After about 15 min . the starting material had dissolved completely . Bubbling of allene was continued for 1 hr . , then the solution was ...
Page 1585
... temperature - independent - paramagnetism ( T.I.P. ) contribution to the susceptibility is calculated using as ... room temperature we are thus justified in writing the mean molar susceptibility , % , for the d2 configuration as NB2 3kT ...
... temperature - independent - paramagnetism ( T.I.P. ) contribution to the susceptibility is calculated using as ... room temperature we are thus justified in writing the mean molar susceptibility , % , for the d2 configuration as NB2 3kT ...
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