Time-resolved resonance Raman spectra of free-base tetraarylporphyrins were obtained to investigate the peripheral substituent effect on the structural changes in the excited states. The aryl mode of H2-tetratoluylporphyrin in the excited triplet state was more strongly enhanced relative to that of
Picosecond time-resolved resonance Raman spectroscopy of the charge separated state of Mg-free base diporphyrins
β Scribed by H. Zhang; E. Schmidt; W. Wu; C.K. Chang; G.T. Babcock
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 543 KB
- Volume
- 234
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The photoinduced charge separated state of a covalently linked magnesium porphyrin and free base porphyrin heterodimer complex (Mg-H 2) was investigated by picosecond time-resolved, two-color, pump-probe resonance Raman spectroscopy. The charge separated state is detected within 30 ps of laser excitation; recombination occurs within 500 ps. In the charge separated state of the Mg-H 2 diporphyrin complex, vibrational mode correlations showed that the magnesium porphyrin cation half of the dimer is in its 2mlu electronic state and the free base porphyrin anion half of the charge transfer state has vibrational characteristics that are interpreted in terms of data available on the free base octaethylporphyrin anion.
π SIMILAR VOLUMES
Pump/probe time-resolved resonance Raman experiments were carried out for free-base octaetbylporphyrin in benzene at room temperature by using two Nd: YAG lasers, and the vibrational spectra of its lowest excited singlet and triplet states were observed. The spectrum of the S, state of OEPHz pumped
Structures and dynamics of the excited electronic states, and and cation radical of 5-dibenzosuberene S 1 T 1 , R ' (DBCH) and its derivatives were investigated in the picosecond-nanosecond time domain using time-resolved resonance Raman spectroscopy with the aid of time-resolved absorption spectros