DIFFUSE-REFLECTANCE LASER PHOTOLYTIC STUDIES OF NAPHTHALENE, BIPHENYLAND SOME AROMATIC-HYDROCARBONS ADSORBED IN THE CAVITIES OF FAUJASITICZEOLITES

Citation
S. Hashimoto et al., DIFFUSE-REFLECTANCE LASER PHOTOLYTIC STUDIES OF NAPHTHALENE, BIPHENYLAND SOME AROMATIC-HYDROCARBONS ADSORBED IN THE CAVITIES OF FAUJASITICZEOLITES, Journal of the Chemical Society. Faraday transactions, 92(19), 1996, pp. 3653-3660
Citations number
74
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
ISSN journal
09565000
Volume
92
Issue
19
Year of publication
1996
Pages
3653 - 3660
Database
ISI
SICI code
0956-5000(1996)92:19<3653:DLPSON>2.0.ZU;2-J
Abstract
Time-resolved absorption and emission characteristics of naphthalene, biphenyl and a few other aromatic molecules adsorbed in the cavities o f zeolites NaX and NaY have been investigated as a function of sample loading. At low loadings, biphotonic ionization was observed to genera te both the radical cations of guest aromatic species and trapped elec trons in the zeolite frameworks. Different types of trapped electrons were found depending on the hydration levels of the zeolite, i.e. Na-4 (3+) in dehydrated zeolites and a mixture of Na-3(2+) and Na-2(+) in h ydrated zeolites. As the loading was increased, increased formation of the radical anions of the guest species occurred with a significant d ecrease in the yield of trapped electrons. It was firmly established t hat radical anions are not produced from trapped electrons and neutral molecules on us timescales. We propose, therefore, that they are prod uced from neutral molecules by scavenging photo-ejected electrons befo re they are trapped. This mechanism of anion formation is characterist ic of zeolites in which acceptor molecules with restricted diffusional motions are concentrated in the vicinity of photo-ionized molecules i n cage networks. The dimer cation of naphthalene was also found to be formed photochemically in the zeolite cage networks at high loadings. A specific effect of zeolite cages which facilitates the photochemical reactions of guest organic molecules is described.