Excited-State Vibrational Coherence and Anisotropy Decay in the Bacteriochlorophyll a Dimer Protein B820

• Published in: The journal of physical chemistry. B 1998-04, Vol.102 (15), p.2776-2786
• Main Authors: Diffey, William M, Homoelle, Bradley J, Edington, Maurice D, Beck, Warren F
• Format: Article
• Language: English
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp9723022

We have employed dynamic absorption spectroscopy to monitor coherent wave packet dynamics and anisotropy decays following impulsive excitation of the B820 subunit of the LH1 light-harvesting complex, which was isolated from Rhodospirillum rubrum G9. When the lower exciton-state transition of the bacteriochlorophyll a dimer is pumped, the time-resolved pump−probe spectrum exhibits contributions from a fully Stokes shifted stimulated-emission spectrum and a nonstationary vibrational character within 40 fs of excitation. Coherent wave packet motion in both the ground state and the excited state is observed via modulations of single-wavelength transients. The photobleaching portion of the spectrum exhibits strong components only at low frequencies, 20−60 and 180 cm-1, and a weaker component is observed at 400 cm-1. The stimulated-emission portion of the spectrum exhibits weak modulation components at 20−60 and 180 cm-1, but strong components are observed at fairly high frequencies:  360, 400, 470, 600, and 730 cm-1. An anisotropy decay observed in the stimulated-emission region reports a prompt >20° tilt of the photoselected transition-dipole moment. A possible explanation for these results is that an intradimer charge-transfer event occurs on a very short time scale following optical preparation of the lower π → π* exciton state of the bacteriochlorophyll a dimer at room temperature.