Supramolecular chirality in crystalline assemblies of bile acids and their derivatives; Three-axial, tilt, helical, and bundle chirality

被引:46
作者
Miyata, Mikiji [1 ]
Tohnai, Norimitsu [1 ]
Hisaki, Ichiro [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
来源
MOLECULES | 2007年 / 12卷 / 08期
关键词
steroidal bile acids; inclusion crystal; supramolecular chirality; helices; molecular tilt;
D O I
10.3390/12081973
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Steroidal bile acids and their derivatives exhibit characteristic inclusion behaviors in the crystalline state. Their crystals present varied assemblies due to asymmetric molecular structures, which relate to supramolecular properties through cooperative weak interactions. An overview indicates that the steroidal assemblies lie in an intermediate position among various molecules and have hierarchical structures such as primary, secondary, tertiary, and host-guest assemblies like proteins. Such an interpretation brought about the idea that the assemblies with dimensionality present supramolecular chirality such as three-axial, tilt, helical, bundle, and complementary chirality. This concept of the supramolecular chirality enables us to understand formation of chiral crystals starting from the molecular chirality of the steroidal molecules.
引用
收藏
页码:1973 / 2000
页数:28
相关论文
共 134 条
  • [1] Dependence of the enantioselectivity on reversion of layer directions in cholamide inclusion compounds
    Aburaya, Kazuaki
    Hisaki, Ichiro
    Tohnai, Norimitsu
    Miyata, Mikiji
    [J]. CHEMICAL COMMUNICATIONS, 2007, (41) : 4257 - 4259
  • [2] [Anonymous], COMPREHENSIVE SUPRAM
  • [3] Aoki Y, 2000, ENANTIOMER, V5, P95
  • [4] CRYSTAL AND MOLECULAR-STRUCTURE OF LITHOCHOLIC ACID
    ARORA, SK
    GERMAIN, G
    DECLERCQ, JP
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1976, 32 (FEB15): : 415 - 419
  • [5] ATWOOD JL, 1984, INCLUSION COMPUNDS, V1
  • [6] Enantioselective inclusion in bile acids: resolution of cyclic ketones
    Bertolasi, V
    Bortolini, O
    Fogagnolo, M
    Fantin, G
    Pedrini, P
    [J]. TETRAHEDRON-ASYMMETRY, 2001, 12 (10) : 1479 - 1483
  • [7] Bile acid derivatives as enantiodifferentiating host molecules in inclusion processes
    Bortolini, O
    Fantin, G
    Fogagnolo, N
    [J]. CHIRALITY, 2005, 17 (03) : 121 - 130
  • [8] Optical resolution of cyclic amides by inclusion in dehydrocholic acid
    Bortolini, O
    Fogagnolo, M
    Fantin, G
    Medici, A
    [J]. CHEMISTRY LETTERS, 2003, 32 (03) : 206 - 207
  • [9] Optical resolution of sulfoxides by inclusion in host dehydrocholic acid
    Bortolini, O
    Fantin, G
    Fogagnolo, M
    Medici, A
    Pedrini, P
    [J]. CHEMICAL COMMUNICATIONS, 2000, (05) : 365 - 366
  • [10] Resolution of unfunctionalized epoxides by cholic acid inclusion compounds
    Bortolini, O
    Fantin, G
    Fogagnolo, M
    Medici, A
    Pedrini, P
    [J]. CHEMISTRY LETTERS, 2000, (11) : 1246 - 1247