Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 408
1 · 3 × 10-3 N m - 2 for 12 h at 673 K is shown in Figure ( la ) . † The low - field part of this spectrum , associated with g1 , is H ( a ) caused a gradual reduction in the total intensity of the e.s.r. spectrum .
1 · 3 × 10-3 N m - 2 for 12 h at 673 K is shown in Figure ( la ) . † The low - field part of this spectrum , associated with g1 , is H ( a ) caused a gradual reduction in the total intensity of the e.s.r. spectrum .
Page 485
36 ( 1 ) H ( 6 ) -98 ・ 0161 H 54 58 ( 5 ) -34 40 H H O - 33 60-35 -31 16/14 ) -91 ( 2 ) H 26 8 ( 3 ) CH3 ( 10 ) H 31 CH3 ( 7 ) X -14 FIGURE 1 CH3 CH3 CH2CH3 in a 2,2 - dimethyldioxolan derivative has now been calcu- lated from X - ray ...
36 ( 1 ) H ( 6 ) -98 ・ 0161 H 54 58 ( 5 ) -34 40 H H O - 33 60-35 -31 16/14 ) -91 ( 2 ) H 26 8 ( 3 ) CH3 ( 10 ) H 31 CH3 ( 7 ) X -14 FIGURE 1 CH3 CH3 CH2CH3 in a 2,2 - dimethyldioxolan derivative has now been calcu- lated from X - ray ...
Page 737
아 2.0 2 [ A ] P ( CO ) ( cm Hg ) 2.0- [ B ] 0 12 2 P ( N2OXcm Hg ) 12 16 FIGURE 1. Effect of CO pressure on the reaction rates ( A ) and the effect of NO pressure on the reaction rates ( B ) . ( A ) : Photocatalytic reaction .
아 2.0 2 [ A ] P ( CO ) ( cm Hg ) 2.0- [ B ] 0 12 2 P ( N2OXcm Hg ) 12 16 FIGURE 1. Effect of CO pressure on the reaction rates ( A ) and the effect of NO pressure on the reaction rates ( B ) . ( A ) : Photocatalytic reaction .
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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 |
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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