SUBPICOSECOND PUMP-SUPERCONTINUUM PROBE SPECTROSCOPY OF LH2 PHOTOSYNTHETIC ANTENNA PROTEINS AT LOW-TEMPERATURE

Citation
A. Freiberg et al., SUBPICOSECOND PUMP-SUPERCONTINUUM PROBE SPECTROSCOPY OF LH2 PHOTOSYNTHETIC ANTENNA PROTEINS AT LOW-TEMPERATURE, The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 102(23), 1998, pp. 4372-4380
Citations number
52
Categorie Soggetti
Chemistry Physical
ISSN journal
10895639
Volume
102
Issue
23
Year of publication
1998
Pages
4372 - 4380
Database
ISI
SICI code
1089-5639(1998)102:23<4372:SPPSOL>2.0.ZU;2-M
Abstract
Exciton relaxation and energy-transfer processes in the B850 circular aggregate of bacteriochlorophyll a molecules from the purple nonsulfur photosynthetic bacterium Rhodobacter sphaeroides were studied at temp eratures below 18 K. Excitons were selectively excited by a 7 nm spect ral bandwidth pump pulse resonant with the inhomogeneously broadened l ong-wavelength side of the B850 ground-state absorption spectrum (betw een 860 and 879 nm). The transient spectra were measured over the 786- 924 nm spectral range using a white light continuum probe pulse. Chara cteristic changes of transient spectra were observed over 4 decades of time, from about 10(-13) to about 10(-9) s. The spectral evolution wa s pump wavelength-dependent, changes being least notable at far-red ex citation. A simple model was put forward to interpret the data, assumi ng that the sample consists of an ensemble of spectrally disorded exci tons, each representing a separate B850 ring. It was found that the ex citon coupling and diagonal disorder play almost equally important rol es in the formation of the spectral and dynamical properties of Light excitations in B850 antenna. The main effects of disorder considered w ere the spectral shifts, splitting of the degenerate exciton levels, a nd redistribution of the dipole strength of the transitions. Assuming that the contribution of least disturbed excitons is largest near the peak of the ground-state absorption spectrum and greatest near the edg e, most of the known spectroscopic properties of LH2, complexes can be well understood, at least qualitatively. Specifically, the rough 100 fs response time was assigned to interexciton level relaxation; the th ree time constants, ca. 800 fs, ca. 15 ps, and ca. 150 ps, were attrib uted to exciton energy transfer, most likely, between the B850 rings. The ca. 1 ns decay time is due to the finite exciton lifetime. The cir cular LH1 antennas likely possess similar properties.