Table of Contents
Laser Chemistry
Volume 19 (1999), Issue 1-4, Pages 271-274
http://dx.doi.org/10.1155/1999/82824

Time-Resolved Resonance Raman Spectroscopy of Excited-State Porphyrins

1School of Chemistry, The Queen's University of Belfast, Belfast BT9 5AG, United Kingdom
2Dept. of Chemistry, University of York, Heslington, York Y01 5DD, United Kingdom
3Institute for Molecular Science, Okazaki National Research Institutes, Myodaiji, Okazaki 444, Japan

Received 11 April 1997

Copyright © 1999 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Time-resolved resonance Raman (TR3) and absorbance difference studies of the excited states of Cu(TPP) (TPP=5,10,15,20-tetraphenylporphyrin) have been carried out with < 10 ps times resolution in THF and pyridine solvents. In THF the distinctive transient Raman bands in the ν2 and ν4 regions, previously observed with ns laser pulses, grow in the first 55 ps before decaying in 100's of ps. The ∆A spectra also show biphasic decay. This behaviour is associated with attack by solvent on the 4-coordinate excited state to form the longer lived species observed in TR3 experiments.

In pyridine two component decay is also observed but it is the shorter-lived species which gives the transient Raman bands seen previously with ns laser excitation. This state is different from that seen in THF. At 5 ps delay ν4 is broader than in the ground state and, more importantly, there is a significant shift in the two pyridine bands at ca. 1000 cm-1. This implies a significant involvement of the pyridine-based orbitals in the excited state.