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Title: Transient absorption spectroscopy of bacteriochlorophyll a: Cation radical generated in solvents forming aggregates and T[sub 1] species generated in solvents forming penta- and hexacoordinated monomers with and without hydrogen bonding

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100097a039· OSTI ID:6620040
;  [1];  [2]
  1. Kwansei Gakuin Univ., Nishinomiya (Japan)
  2. Kobe City Univ. of Foreign Studies (Japan)

Transient absorption spectra of bacteriochlorophyll a were recorded at room temperature in 16 different solvents 200 ns after excitation. The cation radical was found in carbon tetrachloride forming higher aggregates, both the cation radical and the T[sub 1] species were found in methylene chloride forming lower aggregates, and the T[sub 1] species was found in the rest of the solvents forming monomers. Thus, the cation radical can be formed in the aggregates upon photoexcitation. The T[sub 1] [yields] T[sub n] absorption spectra exhibited the following solvent effects: (1) In non-hydrogen-bonding solvents, the lowest-energy peak shifted to the lower energies upon transformation from the penta- to hexacoordinated state. (2) In hydrogen-bonding solvents (alcohols), the transformation caused the low-energy shifts of the lower three peaks as well as the appearance of a new split peak. (3) Replacement of a non-hydrogen-bonding solvent by a hydrogen-bonding solvent, in the same state of coordination, also caused the low-energy shifts of the above absorption peaks. 19 refs., 4 figs., 2 tabs.

OSTI ID:
6620040
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 98:46; ISSN 0022-3654
Country of Publication:
United States
Language:
English

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