G. Balakrishnan et al., RESONANCE RAMAN AND INFRARED SPECTRAL STUDIES ON RADICAL-ANIONS OF MODEL PHOTOSYNTHETIC REACTION-CENTER QUINONES (NAPHTHOQUINONE DERIVATIVES), Journal of biomolecular structure & dynamics, 16(1), 1998, pp. 123-131
Quinones play a vital role in the processes of electron transfer in ba
cterial photosynthetic reaction centers. It is of interest to investig
ate photochemical reactions involving quinones with a view to elucidat
e structure-function relationships in biological processes. Resonance
Raman and FTIR spectra of electrochemically generated radical anions o
f 2-methyl-1,4-naphthoquinone, and 2-methyl-3-phytyl-1,4-naphthoquinon
e, also known as Vitamin K-3 and Vitamin K-1, respectively, (model com
pound for Q(A) in Rhodopseudomonas viridis, a bacterial photosynthetic
reaction center) have been reported. The same study has also been ext
ended to 1,4-naphthoquinone for comparison. The vibrational assignment
s were carried out on the basis of comparison with our earlier time re
solved resonance Raman studies on photochemically generated radical an
ions of 1,4-naphthoquinone and 2-methyl-1,4-naphthoquinone (Balakrishn
an er al., J. Phys. Chern., 100, (1996), 16472-16478). These in vitro
results have been compared with the reported vibrational spectral data
under in vivo conditions.