Functional organic gels. Enantioselective elution using chiral gels from amino acid-derived lipids

Liquid Crystals

Volumn 20, Issue 6, 1996, Pages 807-809

  Ihara, Hirotaka ^a   Shudo, Ken ^a   Hirayama, Chuichi ^a   Hachisako, Hiroshi ^b   Yamada, Kimiho ^b  

^a KUMAMOTO UNIVERSITY   (Japan)

^b SOJO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001154858     PISSN: 02678292     EISSN: 13665855     Source Type: Journal    
DOI: 10.1080/02678299608033175     Document Type: Article

References (8)

1. IHARA, H., HACHISAKO, H., HIRAYAMA, C., and YAMADA, K., 1992, J. Chem. Soc. Chem. Commun., 1234.
2. TAKAFUJI, M., IHARA, H., HIRAYAMA, H., HACHISAKO, C., and YAMADA, K., 1995, Liq. Cryst., 18, 97.
3. MURATA, K., AOKI, M., NISHI, T, IKEDA, A., and SHINKAI, S., 1991, J. Chem. Soc. Chem. Commun., 1715.
4. Lin, Y.-C., Kacher, B., and Weiss, R. G., 1989, J. Am. Chem. Soc., III, 5542.
5. IHARA, H., YAMAGUCHI, M., TAKAFUJI, M., HACHISAKO, H., HIRAYAMA, C., and YAMADA, K., 1990, Nippon Kagaku Kaishi, 1047.
6. This was carried out by calculation with the MOPAC 6 00 program (MATERIA) using the PM3 option [7].
7. Stewart, J. J., 1989, J. Comp. Chem., 10, 221.
8. The elution rate (£D or EL, mol cm “2 h -1) was determined by using the absorbance change of the initial 2h. The enantioselectivity is represented by the ratio (ED/EL) of elution rate for D- and L-enantiomers.