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Studies of the vibrational and electronic structure of the S{sub 1} excited states of {beta}-substituted porphyrins by picosecond time-resolved resonance Raman spectroscopy

Journal Article · · Journal of Physical Chemistry
; ; ; ;  [1];  [2]
  1. Princeton Univ., NJ (United States)
  2. Pacific Northwest Lab., Richland, WA (United States)

Resonance Raman (RR) spectra are reported for the S{sub 1} excited states of zinc(II) complexes of octaethylporphyrin (OEP) and protoporphyrin-IX-dimethyl ester (PPDME). Skeletal stretching modes exhibit large downshifts in the S{sub 1} state of ZnOEP relative to the ground state, indicating an overall expansion of the macrocycle upon photoexcitation. Vibrational modes are assigned using {sup 15}N and meso-d{sub 4} isotopomers of OEP: the isotopic sensitivity is observed to be similar in the S{sub 0} and S{sub 1} states, implying that the ground-state normal mode structure is preserved in the singlet excited state. Excited-state bond orders are calculated using INDO1/S methods. The frequency shift patterns for skeletal vibrational modes of ZnPPDME in the S{sub 1} excited state closely resemble those of ZnOEP, implying a similar electronic configuration; the vinyl C=C stretching mode appears to be only slightly perturbed in the excited states, although the exact position cannot be accurately determined. The results of these studies support the description of metalloporphyrin singlet excited states provided by Gouterman`s four-orbital model. 69 refs., 9 figs., 3 tabs.

Sponsoring Organization:
USDOE
DOE Contract Number:
AC02-81ER10861; AC06-76RL01830
OSTI ID:
45002
Journal Information:
Journal of Physical Chemistry, Journal Name: Journal of Physical Chemistry Journal Issue: 16 Vol. 99; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English