A suspension containing an equimolecular amount of (-)-gallocatechin-3-O- gallate (GCg) and caffeine in water was heated at 90°C for 30 min to give a 1 : 2 complex of GCg and caffeine. X-Ray crystallographic analysis of crystal of the 1 : 2 complex showed that π-π interactions formed between the A, B' rings of GCg and the two six-membered rings of caffeine. Whereas, the same suspension was heated at 90°C for 30 s to give a sticky substance, which contained GCg, caffeine, and water at a molar ratio of 1 : 1 : 22 based on measurement of the integral volume of 1H-NMR signals. The sticky substance crystallized slowly to give a 2 : 2 complex of GCg and caffeine. X-Ray crystallographic analysis of crystal of the 2 : 2 complex showed that the A and C rings of GCg moieties faced each other, and face-to-face π-π interactions formed between the B ring of GCg and caffeine, the B' ring of GCg and caffeine. © 2011 Pharmaceutical Society of Japan.
CITATION STYLE
Tsutsumi, H., Sato, T., & Ishizu, T. (2011). Stereochemical structure and intermolecular interaction of complexes of (-)-gallocatechin-3-O-gallate and caffeine. Chemical and Pharmaceutical Bulletin, 59(1), 100–105. https://doi.org/10.1248/cpb.59.100
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