Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
From inside the book
Results 1-3 of 72
Page 152
... constants for reactions of OH with charged and neutral surfactants are substantially smaller above the critical micelle concentrations than below them ; rate constants for OH addition to CH , are also smaller in micellar systems than in ...
... constants for reactions of OH with charged and neutral surfactants are substantially smaller above the critical micelle concentrations than below them ; rate constants for OH addition to CH , are also smaller in micellar systems than in ...
Page 239
... constants in the chlorobenzenes . In order to carry out calculations for these , we needed the MINDO / 2 parameters for CC1 , HCl , and CICI interactions . These were determined as before by fitting the heats of formation and bond ...
... constants in the chlorobenzenes . In order to carry out calculations for these , we needed the MINDO / 2 parameters for CC1 , HCl , and CICI interactions . These were determined as before by fitting the heats of formation and bond ...
Page 435
... constants for the formation of π - molecular complexes are usually determined by measuring the con- centration - dependent intensity of an intermolecular charge transfer band . The equilibrium constants so determined Several initial ...
... constants for the formation of π - molecular complexes are usually determined by measuring the con- centration - dependent intensity of an intermolecular charge transfer band . The equilibrium constants so determined Several initial ...
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
Bibliographic information
| Title | Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
| Author | Chemical Society (Great Britain) |
| Contributor | Royal Society of Chemistry (Great Britain) |
| Published | 1971 |
| Original from | the University of Michigan |
| Digitized | 22 Mar 2006 |
| Export Citation | BiBTeX EndNote RefMan |