Enantioselective recognition by a highly ordered porphyrin-assembly on a chiral molecular gel |
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Authors: | Jintoku Hirokuni Takafuji Makoto Oda Reiko Ihara Hirotaka |
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Institution: | Department of Applied Chemistry and Biochemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan. |
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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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