Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1065
... range 0.1-1.0N range 1.0-3.5N Molality range 0.1-5.0m a + 4-728318 +4.728316 10-16-0924 b 10-26-642185 10-2 • -6.990515 10-1 . - 1.52306 C 10-38.187141 d e f -1.931383 10-21.263947 10-4 +3.626550 10-37.555687 10-21.828010 10-3.1.456715 ...
... range 0.1-1.0N range 1.0-3.5N Molality range 0.1-5.0m a + 4-728318 +4.728316 10-16-0924 b 10-26-642185 10-2 • -6.990515 10-1 . - 1.52306 C 10-38.187141 d e f -1.931383 10-21.263947 10-4 +3.626550 10-37.555687 10-21.828010 10-3.1.456715 ...
Page 1189
... range of chloride com- plexes investigated . Examination of the spectra over a temperature range show that in the melts the broad singlet , where observed , may be resolved into a doublet on cooling , whilst the opposite trend tends to ...
... range of chloride com- plexes investigated . Examination of the spectra over a temperature range show that in the melts the broad singlet , where observed , may be resolved into a doublet on cooling , whilst the opposite trend tends to ...
Page 1190
... range studied , 60-200 ° , the x - proton signal is a doublet ( Figure 1 ) . ( c ) 4 - Pr " CH , N , AIX , ( X = Br , I ) . Both iodide and bromide were broad over the temperature range 40-60 ° . This persisted in the iodide as the ...
... range studied , 60-200 ° , the x - proton signal is a doublet ( Figure 1 ) . ( c ) 4 - Pr " CH , N , AIX , ( X = Br , I ) . Both iodide and bromide were broad over the temperature range 40-60 ° . This persisted in the iodide as the ...
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