MOLECULES WITH LARGE CAVITIES IN SUPRAMOLECULAR CHEMISTRY

被引:252
作者
SEEL, C [1 ]
VOGTLE, F [1 ]
机构
[1] UNIV BONN, INST ORGAN CHEM & BIOCHEM, GERHARD DOMAGK STR 1, W-5300 BONN 1, GERMANY
关键词
D O I
10.1002/anie.199205281
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supramolecular chemistry is a new area of research that has rapidly developed from pure synthetic chemistry, and its novelty has led to interdisciplinary cooperation between organic and inorganic chemistry, biochemistry, physical and theoretical chemistry, and physics. Whereas molecular chemistry essentially deals with the covalent bonding of atoms, Supramolecular chemistry is predominantly involved in the study of the weaker intermolecular interactions resulting in the association and self‐organization of several components to form larger aggregates (supramolecules). The first crown ether discovered by the subsequent Nobel prizewinner Pedersen was more the fortuitous reaction product of an impurity, but nowadays, some twenty‐five years later, chemists are able to tailor host molecules to special requirements. Host compounds having a cyclophane skeleton make an important contribution, since their aromatic structural units ensure the necessary rigidity of the molecular structures and thereby improve the preorganization of the coordination sites for the cooperative binding of the guests. During the course of the rapid development of Supramolecular chemistry such a large number of synthetic hosts has been developed and their interaction with guests studied in such depth that we must restrict ourselves here to a discussion of a particular group of host compounds, namely cavity‐supporting macrobicyclic and macrooligocyclic phanesu, which bear a similar relation to open‐chain and monocyclic hosts as the metal‐complexing cryptands to the podands and crown ethers. The molecular architecture of these three‐dimensionally bridged macrooligocycles is a challenge for synthetic chemistry. (Not only the size and shape of the intramolecular cavity, but also the provision of the latter with suitable coordination centers have to be included in the synthesis strategy.) The capacity for the envelopment of guests from all sides and the expedient endo functionalization often also produce a particularly strong binding of host and guest, outstanding selectivities with regards to molecular recognition, and special properties of the Supramolecular complexes. Copyright © 1992 by VCH Verlagsgesellschaft mbH, Germany
引用
收藏
页码:528 / 549
页数:22
相关论文
共 342 条
  • [21] 2ND-SPHERE PHOTOCHEMISTRY AND PHOTOPHYSICS OF COORDINATION-COMPOUNDS
    BALZANI, V
    SABBATINI, N
    SCANDOLA, F
    [J]. CHEMICAL REVIEWS, 1986, 86 (02) : 319 - 337
  • [22] BALZANI V, 1990, TOP CURR CHEM, V158, P31
  • [23] BALZANI V, 1986, HOMOGENEOUS HETEROGE
  • [24] BALZANI V, 1991, SUPRAMOLECULAR PHOTO
  • [25] Balzani V., 1987, SUPRAMOLECULAR PHOTO
  • [26] CAGED AND UNCAGED RUTHENIUM(II) POLYPYRIDINE COMPLEXES - COMPARATIVE-STUDY OF THE PHOTOCHEMICAL, PHOTOPHYSICAL, AND ELECTROCHEMICAL PROPERTIES
    BARIGELLETTI, F
    DECOLA, L
    BALZANI, V
    BELSER, P
    VONZELEWSKY, A
    VOGTLE, F
    EBMEYER, F
    GRAMMENUDI, S
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (13) : 4662 - 4668
  • [27] BARIGELLETTI F, 1987, PHOTOCHEM PHOTOBIOL, P79
  • [28] Bauer M., UNPUB
  • [29] TORAND SYNTHESIS BY TRIMERIZATION - NEW RECEPTORS FOR GUANIDINIUM
    BELL, TW
    LIU, J
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1990, 29 (08) : 923 - 925
  • [30] BELL TW, 1990, ANGEW CHEM, V102, P931