Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
From inside the book
Results 1-3 of 74
Page 77
Using the structural framework shown in Figure 1 , the results can be explained by invoking a bridge tauto- merization in which the bridge hydrogen moves rapidly first - mentioned mechanism , is that the bridge hydrogen is located ...
Using the structural framework shown in Figure 1 , the results can be explained by invoking a bridge tauto- merization in which the bridge hydrogen moves rapidly first - mentioned mechanism , is that the bridge hydrogen is located ...
Page 148
Substituent Effects on the Rate of Reaction of Aqueous Hydrogen ( Tritium ) Atoms with Aromatic Compounds By C. L. BRETT and V. GOLD * ( Department of Chemistry , King's College , London , WC2R 2LS ) replacement at the site of tritium ...
Substituent Effects on the Rate of Reaction of Aqueous Hydrogen ( Tritium ) Atoms with Aromatic Compounds By C. L. BRETT and V. GOLD * ( Department of Chemistry , King's College , London , WC2R 2LS ) replacement at the site of tritium ...
Page 337
Infrared Spectroscopic Study of the Hydrates of Hydrogen Chloride and Hydrogen Bromide By A. S. GILBERT and N. SHEPPARD * ( School of Chemical Sciences , University of East Anglia , Norwich NOR 88C ) around 950-900 cm - 1 .
Infrared Spectroscopic Study of the Hydrates of Hydrogen Chloride and Hydrogen Bromide By A. S. GILBERT and N. SHEPPARD * ( School of Chemical Sciences , University of East Anglia , Norwich NOR 88C ) around 950-900 cm - 1 .
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
Page | 1 |
Electrochemical Indications of New Oxidation States in Transitionmetal Dicarbollide Complexes | 8 |
Synthesis of a 1026Pyridinophane by U K GEORGI and J RÉTEY | 32 |
15 other sections not shown
Other editions - View all
Common terms and phrases
acetate acid addition alcohol Amer analysis appears aromatic assigned atoms band bond calculated carbon carbonyl Chem Chemical Chemistry chloride chromatography co-ordination Comm complexes compounds concentration configuration confirmed consistent constants containing corresponding coupling Crystal Department of Chemistry derivatives determined effect electron ester ether evidence expected experiments Figure followed formation formed gave give hydrogen indicate intermediate involving isolated ligand mass measured mechanism metal method methyl mixture molecular molecule n.m.r. spectrum nitrogen observed obtained occurs oxidation oxygen peak position possible prepared presence protons radical ratio reaction rearrangement Received recently reduction relative reported Research resonance respectively ring Scheme shift shown shows signals similar solution solvent space group spectra spectrum structure studies substituted suggested Summary synthesis Table temperature Tetrahedron Letters thank tion University values X-ray yield