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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2109-2117 
    ISSN: 1434-193X
    Keywords: Catenanes ; Molecular recognition ; Polycatenanes ; Self-assembly ; Template-directed synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A main-chain poly([2]catenane), incorporating an average of 25 repeating [2]catenane units and having an Mn value of 35 kg mol-1, was synthesized by the polyesterification of a [2]catenane monomer composed of a bipyridinium-based tetracationic cyclophane mechanically interlocked with a 1,5-dioxynaphthalene-based macrocyclic polyether. Similarly, two main-chain poly(bis[2]catenane)s, both incorporating an average of 15 repeating bis[2]catenane units and both having Mn values of 45 kg mol-1, were prepared by the copolymerizations of a bis[2]catenane monomer, possessing two hydroxymethyl functions with an appropriate bis(isocyanate). The same copolymerization was employed in order to produce a pendant poly([2]catenane), incorporating an average of 20 repeating [2]catenane units and having an Mn value of 27 kg mol-1, from a [2]catenane monomer possessing two hydroxymethyl groups on its macrocyclic polyether component.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2565-2571 
    ISSN: 1434-193X
    Keywords: Molecular recognition ; Rotaxanes ; Self-assembly ; Template-directed synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three dumbbell-shaped compounds incorporating terminal triisopropylsilyl stoppers, connected to a central 1,5-dioxynaphthalene recognition site by [-CH2CH2O-]n spacers (n = 1-3), have been synthesized. These compounds have been employed as templates for the synthesis of [2]rotaxanes incorporating cyclobis(paraquat-p-phenylene) as the ring component. It was found that the length of the polyether chains of the templates influences the efficiencies of the template-directed syntheses. Rotaxane formation occurs only if n 〉 1 and, when n = 3 the corresponding [2]rotaxane can be isolated in a yield as high as 72 %. This remarkable yield is the highest ever obtained for the template-directed syntheses of [2]rotaxanes incorporating donor/acceptor interactions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0947-3440
    Keywords: Crown compounds ; Molecular knots ; Self-assembly ; Supramolecular chemistry ; Template-directed synthesis ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A design logic for the self-assembly of a molecular trefoil knot and of its isomeric trivial knot is described. The approach relies on the formation of a double-stranded supramolecular complex between an acyclic π-electron rich 1,5-di-oxynaphthalene-based polyether and an acyclic π-electron deficient bipyridinium-based tetracation. The reversible complexation of the two acyclic complementary components in solution is followed by the irreversible formation of covalent bonds connecting the termini of these two precursors within the supramolecular complex, affording both a trefoil knot and a trivial knot, though only in extremely low yields. The isomers were separated by preparative high-performance liquid chromatography and characterized by liquid secondary ion mass spectrometry which revealed the binding of up to two ammonium ions in the case of only one of the two isomers - namely, the trivial knot. In addition, we have performed binding studies between some model acyclic and macrocyclic 1,5-dioxynaphthalene-based polyethers and the bipyridinium based precursor of the knots. One of the complexes was also characterized in the solid state by X-ray crystallography which revealed the formation of a [2]pseudorotaxane in the solid state.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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