CH/π hydrogen bonds in crystals

被引:1376
作者
Nishio, M [1 ]
机构
[1] CHPI Inst, Machida, Tokyo 1940043, Japan
来源
CRYSTENGCOMM | 2004年 / 6卷
关键词
D O I
10.1039/b313104a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The nature and characteristics of the CH/pi interaction are discussed by comparison with other weak molecular forces such as the CH/O and OH/pi interaction. The CH/pi interaction is a kind of hydrogen bond operating between a soft acid CH and a soft base pi-system (double and triple bonds, C-6 and C-5 aromatic rings, heteroaromatics, convex surfaces of fullerenes and nanotubes). The consequences of CH/pi hydrogen bonds in supramolecular chemistry are reviewed on grounds of recent crystallographic findings and database analyses. The topics include intramolecular interactions, crystal packing (organic and organometallic compounds), host/guest complexes (cavity-type inclusion compounds of cyclodextrins and synthetic macrocyclic hosts such as calixarenes, catenanes, rotaxanes and pseudorotaxanes), lattice-inclusion type clathrates (including liquid crystals, porphyrin derivatives, cyclopentadienyl compounds and C-60 fullerenes), enantioselective clathrate formation, catalytic enantioface discriminating reactions and solid-state photoreaction. The implications of the CH/pi concept for crystal engineering and drug design are evident.
引用
收藏
页码:130 / 158
页数:29
相关论文
共 573 条
  • [1] PREFERRED CONFORMATION OF 1-PHENYL-2-PROPANOL - ABINITIO AND MOLECULAR MECHANICS CALCULATIONS WITH GEOMETRY OPTIMIZATION
    ABE, K
    HIROTA, M
    MOROKUMA, K
    [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1985, 58 (09) : 2713 - 2714
  • [2] A persistent C-H•••C(π) t-stacked cation
    Abernethy, CD
    Macdonald, CLB
    Clyburne, JAC
    Cowley, AH
    [J]. CHEMICAL COMMUNICATIONS, 2001, (01) : 61 - 62
  • [3] Chemical double-mutant cycles for the measurement of weak intermolecular interactions: Edge-to-face aromatic interactions
    Adams, H
    Carver, FJ
    Hunter, CA
    Morales, JC
    Seward, EM
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (13-14): : 1542 - 1544
  • [4] Substituent effects on aromatic interactions in the solid state
    Adams, H
    Bernad, PL
    Eggleston, DS
    Haltiwanger, RC
    Harris, KDM
    Hembury, GA
    Hunter, CA
    Livingstone, DJ
    Kariuki, BM
    McCabe, JF
    [J]. CHEMICAL COMMUNICATIONS, 2001, (16) : 1500 - +
  • [5] POLARIZED C-H GROUPS AS NOVEL HYDROGEN-BOND DONORS IN HYDRYL-F-ALKYL ESTERS - UNEQUIVOCAL EXAMPLES FOR THE PINCHAS-EFFECT
    ADCOCK, JL
    ZHANG, HQ
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (07) : 1999 - 2002
  • [6] Enantiomeric inclusion of α-hydroxy esters by (R)-(1-naphthyl)glycyl-(R)-phenylglycine and the crystal structures of the inclusion cavities
    Akazome, M
    Takahashi, T
    Ogura, K
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (07) : 2293 - 2300
  • [7] Specific inclusion of 1,2-dimethoxybenzene derivatives by crystalline (R)-arylglycyl-(R)-phenylglycines and its structure
    Akazome, M
    Yanagita, Y
    Sonobe, R
    Ogura, K
    [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1997, 70 (11) : 2823 - 2827
  • [8] Enantiomeric recognition of alkyl phenyl sulfoxides by crystalline (R)-phenylglycyl-(R)-phenylglycine
    Akazome, M
    Noguchi, M
    Tanaka, O
    Sumikawa, S
    Uchida, T
    Ogura, K
    [J]. TETRAHEDRON, 1997, 53 (25) : 8315 - 8322
  • [9] Enantioselective inclusion of methyl phenyl sulfoxides and benzyl methyl sulfoxides by (R)-phenylglycyl-(R)-phenylglycine and the crystal structures of the inclusion cavities
    Akazome, M
    Ueno, Y
    Ooiso, H
    Ogura, K
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (01) : 68 - 76
  • [10] Asymmetric recognition of 1-arylethylamines by (R)-phenylglycyl-(R)-phenylglycine and its mechanism
    Akazome, M
    Matsuno, H
    Ogura, K
    [J]. TETRAHEDRON-ASYMMETRY, 1997, 8 (14) : 2331 - 2336