The triplet-triplet electronic excitation transfer from benzophenone IO naphthalene in rigid solutions has been investigated by measuring the non-exponential decay curve of benzophenone phosphorescence using a laser pulse for excitation. The results of measurements were satisfactorily reproduced by
On the rate of triplet excitation transfer in the diffusive limit
β Scribed by Maria A. Davidovich; Robert S. Knox
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 378 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
The useftdness of spectral data in estim;tting intermolecuhr triplet eacitation transfer mtes is found to be rather limited and to depend explicitly on the mechanisms which allow the optical transitions_ Necessar& conditions for the validiry of such use of spectra are given, and the othen\ise required correction factors are discussed and estimated. Dexter's expression [I] for the rate of triplet exciton transfer in the diffusive limit has been used in cakulations of transport quantities in organic crystals [Z-5]. It relates the rate of transfer of triplet excitation from molecule A to B, wAB, to the exchange interaction ener,T /3 between the molecules and to the normalized phosphorescence spectrum fA and triplet absorption spectrum FB of donor A and acceptor B as follows: (1) The connection with the spectra follows from the identification of the vibrational factors involved in the transfer with those occurring in the spectra of the moIecules_ A similar expression had been derived by Fikster [6] for the rate of transfer of singlet excitons with dipole allowed transitions, in which case the matrix eiements involved in the transfer and in the radiative transition of the molecules are the same. nameIy, those of a dipole interaction. However, in the case of triplet excitons, when the transfer is mediated by an exchange interaction the connection * Research supported in part by NSF grant PCM-77-20230_ Dr_ Davidovich acknowledges partial support by the Brazilian agency Conselho National de Pesquisas. * Based on part of a Ph.D_ thesis submitted to the University of Rochester.
π SIMILAR VOLUMES
The kinetics of NADH oxidation by 3 Dawson-type mixed heteropolyanions were studied in buffered aqueous pH = 7 medium, by the stopped flow technique and UV-visible spectroscopy. The log of k was a linear function of the E Β° of the first redox systems of the heteropolyanions with a slope of 16.5 V-1
for the triplet state of quinosdinc in durene and in pcrdeuterated naphthalene (Na'a) with the pulse uturation method. In the N-da host crystai rhe anisotropy is identical for both molecular orientations A and B.