Intermolecular and Intramolecular Excited State Charge Transfer
Author(s) -
Kenneth B. Eisenthal
Publication year - 1983
Publication title -
laser chemistry
Language(s) - English
Resource type - Journals
eISSN - 1026-8014
pISSN - 0278-6273
DOI - 10.1155/lc.3.145
Subject(s) - intramolecular force , intermolecular force , chemistry , excited state , charge (physics) , state (computer science) , transfer (computing) , photochemistry , chemical physics , computational chemistry , atomic physics , stereochemistry , molecule , organic chemistry , quantum mechanics , physics , computer science , algorithm , parallel computing
A primary mechanism of energy relaxation and chemical change inorganic molecules in excited electronic states is charge transfer. 1 Thecharge transfer process can be intermolecular, involving an excitedmolecule and a neighboring molecule, one serving as an acceptor andthe other as a donor molecule, or intramolecular, involving a chargeredistribution in the excited molecule which produces a very largeexcited state dipole moment. In our investigations of the dynamics of these various charge transferprocesses, a picosecond laser pulse was used to excite the moleculesof interest. The charge transfer dynamics were monitored by a varietyof techniques, including transient absorption of the excited chargetransfer complex (exciplex) or ion radicals by a time delayedpicosecond pulse, and fluorescence from the exciplex and from theinitially excited molecule using a picosecond streak camera fordetection.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom