Time-resolved resonance Raman spectroscopy of triplet-state metallated and free-base tetraarylporphyrins

Autor: John J. McGarvey, J. N. Martin Hegarty, Christer B. Aakeröy, Steven E. J. Bell, John N. Moore, Ala H. R. Al-Obaidi, Colin R. Lefley, Ronald E. Hester
Rok vydání: 1995
Předmět:
Zdroj: J. Chem. Soc., Faraday Trans.. 91:411-418
ISSN: 1364-5455
0956-5000
DOI: 10.1039/ft9959100411
Popis: Resonance Raman spectra of the T1 excited states of Zn and free-base tetra-4-sulfonatophenylporphyrin (TPPS) have been recorded at room temperature in aqueous solution using two-colour time-resolved methods. The spectra of both sulfonated molecules are very similar to their tetraphenylporphyrin (TPP) analogues, which have been recorded in THF solution using the same pump–probe conditions, but they have higher signal-to-noise ratios because interference from strong solvent bands is reduced. Although two different T1 spectra of Zn(TPP) have been reported these spectra differ slightly from each other and from the spectrum reported here, which has band positions very close (±6 cm–1) to those of Zn(TPPS). The high S/N ratios obtainable for the water-soluble porphyrins have allowed reliable polarization data to be recorded for their S0 and T1 states. This data set allows a realistic comparison of the changes in bonding associated with excitation of both free-base and Zn tetraarylporphyrins to the T1 state.Semi-empirical (AM1) calculations of the bond-length changes associated with excitation of free-base TPP and the simpler model tetra-4-fluorophenylporphyrin (TFP) to their T1 states follow qualitative predictions based on the orbital coefficients of the HOMO and LUMO involved in the transition. These structural changes accord satisfactorily with the observed changes in frequency on excitation of the vibrational modes of free-base TPP and TPPS. The calculated bond-length changes are strikingly close to those previously calculated for Zn(TFP), where Jahn–Teller effects are expected. The primary effect of the Jahn–Teller distortion in the molecular orbital calculations is to lift the degeneracy of the eg LUMO pair of the Zn complexes. Once this degeneracy is lifted the calculated geometry changes for both free-base and Zn complexes converge because they arise from a HOMO to LUMO excitation between two orbitals which have similar coefficients in both. The observation that the directions of the shifts of most of the vibrational modes in the T1 states of the free-base and Zn porphyrins are the same, supports this general conclusion. The only band which displays significantly different behaviour between the metallated and free-base systems is ν11 which is a B1g mode. This suggests that the Jahn–Teller distortion that lifts degeneracy of the LUMO in the T1 states of the Zn complexes occurs along a B1g coordinate.
Databáze: OpenAIRE
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