One- and two-photon spectra of some selected molecules: A comparative study

Abstract

The complementarity of one-and two-photon spectroscopy has been utilised for throwing light on the following problems of chemical interest: (1) Weak interaction between identical chromophores separated by insulating bridges gives rise to split states of different symmetries. Two-photon spectroscopy (TPA), in conjunction with one-photon absorption (OPA), has been used to identify the states and hence to estimate the magnitude of interaction in bimolecules and trimolecules. From the shifts between the one-and the two-photon spectra, the splittings have been estimated. Calculations confirm that the dominant interaction is the through-bond one. (2) The second type of problem is the identification of g and u vibrations in molecules. We have initiated studies on three molecules in jet-cooled conditions: 9,10-dihydro-anthracene (DHA). 9,10-dihydro-phenanthrene (DHP) and octa-fluoronaphthalene (OFN). Only the one-photon fluorescence excitation spectra have so far been obtained by us and the TPA spectra are under investigation. (3) The third class of molecules discussed here are the Ln 3 + complexes where f"~ f" transitions are intrinsically two-photon allowed. We have studied two GD 3 + single crystals. The CF-splittings, observed clearly in TPA, have been fitted with a parametric model. Some of our observations on the variations of TPA intensity patterns from crystal to crystal, such as circular:linear polarisation ratios, relative intensities of transitions to different J-states, do not quite fit in with the Axe-Judd-Downer model. The discrepancies call for a reappraisal of the role of ligand in the TPA process.