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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1687-1695 
    ISSN: 0009-2940
    Keywords: Host-Guest chemistry ; Inclusion compounds ; Macropolycyclic compounds ; Heterocyclic compounds ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Multiple-Bridged TriphenylmethanesUp to fourfold-bridged macrocyclic compounds bearing triphenylmethane units which form a large molecular cavity were prepared for the first time. The macrobicyclus 4 crystallizes from acetonitrile as 1:1 adduct and from phenylacetonitrile as 1:3 adduct with the respective solvent. The X-ray structures of these complexes are compared with the related 1:5 adduct of 13 with benzene.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1161-1169 
    ISSN: 0009-2940
    Keywords: Azobenzene units ; Dendrimer ; Divergent synthesis ; Solvent inclusion ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dendrimers with bulky repeating units containing up to 43 benzene rings (in 9) have been obtained by using a repetitive divergent synthetic strategy (three generations). The new functional dendrimer 13 containing six azobenzene units at the periphery was synthesized allowing a reversible switching of the shape and size of the molecule upon irradiation. An X-ray structure analysis of the dendritic molecule 3a shows the inclusion of acetonitrile.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1873-1880 
    ISSN: 0009-2940
    Keywords: Complex formation ; Endoreceptors ; Macrobicyclic ligands ; Phenanthroline derivatives ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Macrobicyclic Endoreceptors: Synthesis, Crystal Structure, and Inclusion of Organic GuestsThe macrobicyclic ligand 2 is synthesized in a one-step cyclization procedure. According to an X-ray structure analysis three dichloromethane guest molecules are included inside the cavity, whereas water and methanol are found outside the cavity. The rigid endo preorganization of the nitrogen donors allows the complexation of three 2,9-disubstituted 1,10-phenanthrolines inside the cavity.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1003-1009 
    ISSN: 0009-2940
    Keywords: Diamine ; Host-guest chemistry ; Macrocycle ; Supramolecular chemistry ; Receptor molecule, synthetic ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tailor-Made Host for Piperazine and Related AminesThe 38-membered bis-catechol 4b is obtained by cyclisation of the diacyl dichloride 3c with the diamine 2b in 45% yield, whereas a 68-membered octalactam 7 is formed under similar conditions from 5 and 1b. Bis-catechol 4b is a selective host compound for piperazine (8) and the structurally related diamine 9. Association constants for the 1:1 complexes have been measured by 1H-NMR titration experiments. A nucleobase guest (pterine, 24) was extracted into a hydrochloric acid phase by complex formation with the host 4b. The results are compared with solubility and transport experiments obtained by use of analogous macrobicyclic tris-catechol hosts.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 897-903 
    ISSN: 0009-2940
    Keywords: Dendrimers ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dendrimers and Dendrimer Building Blocks with Trisubstituted Benzene and “Hexacyclene” as Core UnitsThe preparation of new dendritic compounds containing 1,3,5-substituted aromatic units or “hexacyclene” is described. Bulky dendrimers are obtained in few generations starting with polyfunctional core units like 1, 4, 5, 12, and hexacyclene (21). The dendrimers were synthesized by using both the divergent method (for 7) and the convergent method (for 13 and 22). 22 is the first dendrimer containing a crown unit as core.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 31 (1992), S. 528-549 
    ISSN: 0570-0833
    Keywords: Supramolecular chemistry ; Cage compounds ; Cyclophanes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 16 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 33 (1994), S. 375-384 
    ISSN: 0570-0833
    Keywords: Template synthesis ; Self-assembly ; Supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Although the principle of template synthesis has been known since the sixties, surprising discoveries and new applications in the field of supramolecular chemistry over the last decade have provoked a boom in the subject. The synthesis of supramolecular species has been made much more efficient, or even in some cases possible, by the introduction of template ions or molecules. It is not just metal ions that can act as templates. Neutral molecules, electrostatic interactions, and hydrogen bonds also support the formation of binary and tertiary complexes. Energetically favorable conformations then lead to the formation of a specific desired product in high yield. In addition to the discussion of metal ions and neutral molecules as templates, covalent, positive, and negative templates are differentiated. Kinetic and thermodynamic aspects will also be considered in this review, together with the influence of templates on the phenomenon of self-organization. Further developments and applications include the synthesis of oligonucleotides, peptide blocks capable of forming secondary structure, and template polymers. Template synthesis of defined molecular cavities ultimately leads to “inclusion chemistry on a nanometer scale.”
    Type of Medium: Electronic Resource
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