Ultrafast photophysics and photochemistry of [Ni]-bacteriochlorophyll a

Journal Article · Thu Aug 19 04:00:00 EDT 1999 · Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical

DOI:https://doi.org/10.1021/jp991388r· OSTI ID:691307

Musewald, C; Hartwich, G; Lossau, H; Gilch, P; Poellinger-Dammer, F; Michel-Beyerle, M E ^[1]; Scheer, H ^[2]

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1. Technische Univ. Muenchen, Garching (Germany). Inst. fuer Physikalische und Theoretische Chemie
2. Ludwig-Maximilians-Univ. Muenchen (Germany). Botanisches Inst.

The ultrafast photodynamics of bacteriochlorophyll with the central Mg{sup 2+}-ion replaced by Ni{sup 2+} ([Ni]-BChl) in toluene and pyridine have been studied by femtosecond time-resolved fluorescence and absorption spectroscopy with a time resolution of 100 fs in the spectral range of 470--900 nm. Excitation of tetracoordinated [Ni]-BChl in toluene in its red-most absorption band leads to four transient states which decay single-exponentially with lifetimes of 100 fs, 450 fs, 4 ps, 25 ps. Except for the 4 ps component these kinetics arise from an internal conversion cascade conserving the overall multiplicity of the singlet configuration. The spectral characteristics of the intermediates indicate a deactivation process via several {pi}- and metal-centered excited states. The 4 ps kinetic results from a relaxation within the metal d-states caused by a change of size of the central nickel ion upon electronic excitation. A different deactivation pattern is observed for [Ni]-BChl in pyridine, where the central metal is additionally coordinated by two axial solvent molecules. On the basis of their dynamics and their spectral positions, three different intermediates have been identified. The fastest decay with 150 fs reflects an internal conversion process. This is followed by a process that can be approximately described by time constants of 6 and 90 ps. This decay pattern, concomitant with the spectral changes, is attributed to the ejection of the axial solvent ligands accompanied by intersystem crossing. The slowest component has a characteristic time of > 2 ns and is attributed to the rebinding of the pyridine ligands.

• OSTI ID: 691307
• Journal Information: Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical, Journal Name: Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical Journal Issue: 33 Vol. 103; ISSN 1089-5647; ISSN JPCBFK
• Country of Publication: United States
• Language: English

Related Subjects

14 SOLAR ENERGY
CHLOROPHYLL
MAGNESIUM
NICKEL
PHOTOCHEMISTRY
PHOTOSYNTHESIS