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Enantioselective recognition by a highly ordered porphyrin-assembly on a chiral molecular gel
Authors:Jintoku Hirokuni  Takafuji Makoto  Oda Reiko  Ihara Hirotaka
Institution:Department of Applied Chemistry and Biochemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan.
Abstract:Enantioselective recognition of amino acids was achieved by using a highly ordered chiral assembly of achiral porphyrin on a chiral molecular gel. Exceptionally high enantioselectivity was observed for histidine derivatives by monitoring the CD patterns and fluorescence quenching, K(SV) (l): 26.3 × 10(3) M(-1); K(SV)(D)-enantiomer: 7.03 × 10(3) M(-1).
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