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Excited-state transient of vanadyl uroporphyrin I detected by resonance Raman spectroscopy

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100367a044· OSTI ID:6663270
; ;  [1]; ;  [2]
  1. Univ. of New Mexico, Albuquerque (USA)
  2. Sandia National Labs., Albuquerque, NM (USA)
Transient Raman spectroscopy has been used to investigate excited states of vanadyl uroporphyrin I (VOUroP) in both monomeric and dimeric forms. Uroporphyrins are water-soluble porphyrins with propionic and acetic acid groups substituted at the {beta}-pyrrole carbon positions. Monomeric VOUroP in aqueous solution is known to be six-coordinate with a ligand trans to the oxo ligand. Upon dimerization, the sixth ligand site is inaccessible, and a five-coordinate species is observed. At high laser fluence, an excited-state transient is formed in the monomeric species. Raman spectra of this species are most consistent with an {sup 2}A{sub 1u} (a{sub 1u}({pi}) {yields} d{sub xy}) charge-transfer state. In contrast, dimeric VOUroP shows little evidence of an excited state in the transient Raman spectra during a 10-ns laser pulse.
OSTI ID:
6663270
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 94:4; ISSN JPCHA; ISSN 0022-3654
Country of Publication:
United States
Language:
English