Negative shift of chlorophyll a oxidation potential by aggregation in acetonitrile/ionic liquid mixed solvents
Spectroscopic and electrochemical properties of chlorophyll (Chl) a aggregates in mixed solvents of acetonitrile and an ionic liquid, 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF 4), were examined. The red-shifted absorption peak of the Q y band due to Chl a aggregation as well as the log[Ch...
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Published in | Journal of photochemistry and photobiology. A, Chemistry. Vol. 202; no. 2; pp. 191 - 195 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
25.02.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Spectroscopic and electrochemical properties of chlorophyll (Chl)
a aggregates in mixed solvents of acetonitrile and an ionic liquid, 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF
4), were examined. The red-shifted absorption peak of the
Q
y band due to Chl
a aggregation as well as the log[Chl
a aggregate] against log[Chl
a monomer] plot suggested the formation of low-order aggregates such as a dimer. Square wave voltammetry revealed that the first oxidation potential of the Chl
a aggregate in the AN/EMIBF
4 mixed solvents is shifted negatively by 130
mV from that of Chl
a monomer. In comparison with the redox potential of Chl
a in vivo, a tuning mechanism of the redox potentials for photosynthetic species due to dimerization/aggregation is discussed. |
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ISSN: | 1010-6030 1873-2666 |
DOI: | 10.1016/j.jphotochem.2008.12.006 |