Direct observation of the excited-state c i s – t r a n s photoisomerization of bacteriorhodopsin: Multilevel line shape theory for femtosecond dynamic hole burning and its application

• Published in: The Journal of chemical physics 1989-01, Vol.90 (1), p.199-208
• Main Authors: Pollard, W. Thomas, Cruz, Carlos H. Brito, Shank, Charles V., Mathies, Richard A.
• Format: Article
• Language: English
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.456658

A dynamic hole-burning study of light-adapted bacteriorhodopsin (BR568) using 6 fs optical pulses has recently been reported [R. A. Mathies, C. H. Brito Cruz, W. T. Pollard, and C. V. Shank, Science 240, 777 (1988)]. The temporal evolution of the excited state absorption and emission spectra after excitation with 60 fs pulses provides a direct observation of the C13=C14 torsional isomerization of the retinal chromophore on the excited state potential surface. Here, we present a more detailed discussion of these spectra. The transient hole line shapes are then calculated by solving the density matrix equations for the third-order susceptibility of a multilevel system. The resulting equations are written without reference to the individual vibronic transitions by using the absorption correlation function 〈i‖i(t)〉. The calculations show that the sharp features seen at short delays arise from coherence coupling effects which occur when the pump and probe pulses overlap in time. This analysis demonstrates that the hole seen at 60 fs is consistent with the broad homogeneous absorption line shape for BR568 originally predicted from resonance Raman intensities, and points out the utility of 〈i‖i(t)〉, derived from resonance Raman intensity analysis, in understanding femtosecond dynamic hole-burning experiments.