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Excited states of photobiological receptors. II. Chlorophylls, phytochrome, and stentorin
Author(s) -
Song PillSoon,
Chin ChenAn,
Yamazaki Iwao,
Baba Hiroaki
Publication year - 2009
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.560120730
Subject(s) - excited state , chemistry , phytochrome , singlet state , ring (chemistry) , photochemistry , chromophore , excitation , moiety , chlorin , deprotonation , stereochemistry , ion , atomic physics , physics , botany , biology , porphyrin , red light , organic chemistry , quantum mechanics
In this series on the application of configuration analysis (CA) to the electronic excited states of photobiological receptors, we have extended CA to two important photobiological receptors, phytochrome of photomorphogenic and biological clock systems and stentorin of the photophobic response system of stentors. In addition, the effect of substituents in chlorophylls on the electronic excitation of the chlorin and bacteriochlorin ring systems has been examined. The open‐shell calculations of chlorophylls have also been performed. In the singlet excited state of phytochrome, there is a significant charge transfer from ring A to the violin moiety of the phytochrome molecule, with a tendency for the localized excitation in the A ring. The charge transfer contribution to the singlet‐singlet excitation is also significant. These results are correlated with the photomorphogenic transformation of phytochrome which involves deprotonation and/or tautomerism of the ring A in the excited state. In the case of stentorin, the excitation resides largely in the aromatic system, with some charge transfer to the carbonyl groups. The photobiological significance of these results are discussed.