Photochemistry and Photobiology · 1998 · 35 citations · 17 references
Natural SciencesBiophysicsChemistryBiophysical ChemistryMolecular BiophysicsSupramolecular ChemistryIntermolecular ForcesIntermolecular InteractionsMacromolecular AssemblyMolecular InteractionsMolecular SymmetryPhotosynthetic PigmentsMolecular Aggregation
ABSTRACT 13 C‐enriched bacteriochlorophyll c (S[I, E] BChl c F ) was suspended in a 1:3 mixture of methylene chloride and carbon tetrachloride to form an aggregate showing the Q y absorption above 740 nm; changes in the 13 C chemical shifts were traced when methanol was titrated to dissolve the aggregate, and then, the changes were correlated to the ring‐current effects due to the neighboring macrocycles in the aggregate. A pair of aggregate structures has been proposed based on the ring‐current effects on both 1 H and 13 C nuclei; the monomeric units are stacked together to form an inclined column with different sliding directions, in which the y‐axis of the molecule is parallel to the long axis of the column. In order to confirm this pair of models, the ring‐current effects on the 1 H and 13 C nuclei were calculated based on both the magnetic‐dipole and the loop‐current approximations. Further, an application of three‐dimensional F1 13 C‐edited F3 13 C‐filtered heteronuclear single‐quantum correlation‐nuclear Overhauser effect spectroscopy to the above aggregate consisting of a 1:1 mixture of 13 C‐labeled and unlabeled BChl c succeeded in detecting selectively the 1 H– 1 H intermolecular nuclear Overhauser effect correlations, which established the coexistence of the above pair of stacked structures in the aggregate.
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