1978
DOI: 10.1007/bf03055541
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Chemiluminescence as a means of revealing intermediate stages in adsorption and catalysis

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1979
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Cited by 8 publications
(4 citation statements)
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“…Based on various observations of the oxidation of carbon monoxide on ThO 2 , Claudel et al 6 have presented a mechanism of luminescence emission during catalytic oxidation. They concluded that hole-trapped surface states are produced by the chemisorption of CO, and that electron-trapped surface states are produced by the chemisorption of O on ThO 2 .…”
Section: Discussionmentioning
confidence: 99%
“…Based on various observations of the oxidation of carbon monoxide on ThO 2 , Claudel et al 6 have presented a mechanism of luminescence emission during catalytic oxidation. They concluded that hole-trapped surface states are produced by the chemisorption of CO, and that electron-trapped surface states are produced by the chemisorption of O on ThO 2 .…”
Section: Discussionmentioning
confidence: 99%
“…and was defined as “cataluminescence”. Application of the luminescence has been developed as a means of revealing intermediate stages in adsorption and catalysis . In recent years, Nakagawa et al , observed chemiluminescence during the catalytic oxidation of organic vapors on γ-aluminum oxide (γ-Al 2 O 3 ) and γ-Al 2 O 3 activated by Dy 3+ .…”
mentioning
confidence: 99%
“…Application of the luminescence has been developed as a means of revealing intermediate stages in adsorption and catalysis. 2 In recent years, Nakagawa et al 3,4 observed chemiluminescence during the catalytic oxidation of organic vapors on γ-aluminum oxide (γ-Al 2 O 3 ) and γ-Al 2 O 3 activated by Dy 3+ . No further research about this kind of luminescence has been reported besides the three bulk solids mentioned above.…”
mentioning
confidence: 99%
“…Absolute configuration, 176 Activation and reaction volumes, 46 Acylation, 4-(dialkylamino)pyridines in, 34 Alkaloids, isoquinoline, 182 Lauraceae, 57 spirobenzylisoquinoline, 66 Alkanes, oxgenation with super acids, 42 Alkynes, metal complexes in synthesis, 164 natural antimycotic, 99 in pyridine synthesis, 32 Alienes, synthesis of enallenes, 105 Alumina, organic reactions on, 31 Amidyl radicals, reactivity, 123 Amino acids, oi-alkylamino, 132 codon activation, 38 industrial, 95 Angiotensin, 131 Antibiotics, acetylenic antimycotic, 99 sugar components of, 17 Aroma, naturally occurring, 80 structure and, 50 Aromatic cmpds, arene complexes, 165 biosynthesis, 124 by dehydrogenation, 43 multilayered and bridged, 161 natl occ, 13C NMR, 65 polynuclear, 3 Aromatic substitution, of nitro groups, 119 nucleophilic, Sn(ANRORC), 14 by SrnI mechanism, 11 Carbohydrates, binding by proteins, 18 boronate esters, 16 galactomannans, 19 Carbonyliron, stabilization with, 141 Catalysis, acid-base, 1 acylation, by 4-(dialkylamino)pyridines, 34 on alumina surfaces, 31 bifunctional, 101 chemiluminescence in, 84 homogeneous, 4 hydrogenation, 174 phase-transfer, 87,183 polymeric, 39 Chemiluminescence, in absorption, 84 Chlorophyll, 170,172 Cobalt catalysts in pyridine sysnthesis, 32 Complexes, alkyne-transition metal, 164 arene, 165 cation with crown cmpds, 158 chelate, stereochem. 126 of diazo cmpds, 181 organoiron, 140,141 Conductors, organic, electronic struct, 75 Conformation, angiotensin, 131 five-membered rings, 125 nucleoside, by NMR, 81 Coumarins, nat occurring, 79 Crown cmpds, 155-160 Cyanates, 180 Cy...…”
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confidence: 99%