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  • Molecular recognition  (3)
  • Self-assembly  (3)
  • 1995-1999  (6)
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 977-982 
    ISSN: 1434-1948
    Schlagwort(e): Helicates ; Oligobipyridine ligands ; Self-recognition ; NMR titration ; Self-assembly ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oligobipyridine ligands containing one or two imine bridges were found to form double helicates by treatment with copper(I) or silver(I). The properties of the complexes are similar to those of oxapropylene-bridged oligobipyridines. Titration of a mixture of the bis(bipyridine) and the tris(bipyridine) ligands with silver(I) hexafluorophosphate showed that helicates formed with strict self-recognition.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 517-522 
    ISSN: 1434-1948
    Schlagwort(e): Self-assembly ; Tetranuclear CuII complex ; [2 × 2] grid-type complex ; Crystal structure ; Magnetic properties ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ditopic ligand 3 has been synthesized. In its deprotonated form, it reacts with copper(II) ions to form a tetranuclear complex 1 of the [2 × 2] CuII4 grid type, the structure of which has been confirmed by X-ray crystallography. Magnetic studies of complex 1 indicate a very weak antiferromagnetic coupling between the phenoxo-bridged CuII ions.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1421-1428 
    ISSN: 1434-1948
    Schlagwort(e): Grid complexes ; Self-assembly ; Co ; Zn ; Coordination chemistry ; Bis(tridentate) ligands ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The tretrametallic [2 × 2] grid-type complexes 1-4 are formed by self-assembly of the bis(tridentate) ligands 5 and 6 with ZnII and CoII cations. They have been characterized by spectroscopic studies in solution as well as by crystal structure determination. The substituents in the central pyrimidine ring play an important role in terms of geometry and physical properties of the complexes. They induce an orthogonal orientation of the ligand in the complexes which is critical for the formation of ordered monolayers and extended self-organized arrays of grids. The physical properties of the complexes such as metal-metal interaction and π-π* stacking between the ligands may be modulated by changing these substituents.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1415-1420 
    ISSN: 1434-1948
    Schlagwort(e): Combinatorial chemistry ; Molecular recognition ; Functionalized bipyridine metal complexes ; Janus molecules ; Hydrogen bonding ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The functionalized ligands 1 and 2 bearing hydrogen-bonding recognition groups have been synthesized. Their assembly by metal ions such as CuI and PdII having different coordination geometries generates different receptor architectures for the binding of suitable substrates. Addition of the complementary bis(imide) Janus molecules (4-7) to [1a, 2a, CuTf] or to [1b, 2b, Pd(BF4)2] mixtures leads to a moderate selective increase of the fraction of the [(1a)2Cu]+ or [(1b)2Pd]2+ complex depending on the Janus substrate used. Largest enhancements are observed for those Janus substrates that may be expected to display highest geometrical complementarity with the two complexes. These results represent a process directed by target binding based on dynamic combinatorial chemistry.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    ISSN: 1434-193X
    Schlagwort(e): Cyclo-bis-intercaland ; Acridine units ; cis/trans-Azobenzene dicarboxylic acids ; Inclusion compounds ; X-ray structure ; Molecular recognition ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The water soluble acyclic 1 and macrocyclic 2 receptor molecules, based on acridine units, form 1:1 complexes with the cis- or trans-2,2′ and 3,3′-azobenzene dicarboxylate substrates. The stability constants of these complexes, determined by 1H NMR spectroscopy, cover a wide range from 30 to 105M-1, thus displaying very pronounced structure selectivity with respect to both substitution pattern and cis, transconfiguration. The complexes of the cyclo-bis-intercaland receptor 2 are two or three orders of magnitude more stable than those of 1. The inclusion complex of cyclo-bis-intercaland 2 with trans-3,3′- azobenzene dicarboxylate has been isolated and its structure has been determined by X-ray crystallography using synchrotron radiation, confirming the intercalation of the substrate between the acridine residues in the species formed.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    ISSN: 1434-193X
    Schlagwort(e): Dynamic combinatorial chemistry ; Molecular recognition ; Hydrogen bonding ; Hydrazone isomerization ; Barbiturate receptor ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The selection of the receptor presenting the strongest affinity for a barbiturate substrate from a dynamic combinatorial library of constituents differing in structure and conformation/configuration is described. The gradual addition of the barbiturate to an equilibrating mixture of hydrazone isomers leads to the quantitative shift towards a single species, 3, which presents highest complementarity to the substrate and yields the supramolecular entity 3:4.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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