Chiral Recognition of Tetrahelicene Dicarboxylic Acid by Linear Dextrins
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Recognition of the helicity of 1,12-dimethylbenzo[c]phenanthrene-5,8-dicarboxylic acid (<B>1</B>) by linear oligosaccharides has been studied by <SUP>1</SUP>H NMR spectroscopy and capillary zone electrophoresis. Both methods, clearly indicate that maltotetraose, maltopentaose, maltohexaose, and maltoheptaose selectively complex with the (<I>M</I>)-isomer of <B>1</B> as a guest through hydrogen-bonding interaction in water.
- Chemistry Letters
Chemistry Letters 1997(8), 715-716, 1997-08
The Chemical Society of Japan