Effects of Coadsorbed Water on the Mobility of Polyaromatic Hydrocarbons in Zeolite Y

Triplet excited states of pyrene, phenanthrene, and naphthalene have been prepared in zeolite KY by pulsed laser excitation and the influence of coadsorbed water on quenching of these triplet states by ferrocene and the immobile ferrocene derivative ferrocenylmethytrimethylammonium cation (FcMN) has been studied by transient absorption spectroscopy. To make these measurements, probe loadings in KY have been kept deliberately low such that quenching involves migration of molecules from one supercage to another. In all cases, maxima in bimolecular triplet quenching rates versus the number of H 2 O per supercage ( N sc ) were observed at N sc ≈ 4, a value which coincides with the number of H 2 O molecules that fill the sodalite cages. For pyrene quenching by FcMN, the effect of 4 H 2 O/sc was particularly dramatic, where the quenching rate increased by 3 orders of magnitude relative to dehydrated KY. Above N sc = 4, further additions of H 2 O lowered the rate of quenching. The rate of triplet quenching by FcMN, where quenching results from motion of the aromatic probes in their triplet state to FcMN, generally followed the trend 3 Np* > 3 Ph* ≫ 3 Py*. This trend, as well as the influence of coadsorbed H 2 O on quenching, have been explained by the effects of adsorption and molecular size on diffusion of these molecules in KY.