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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1421-1428 
    ISSN: 1434-1948
    Keywords: Grid complexes ; Self-assembly ; Co ; Zn ; Coordination chemistry ; Bis(tridentate) ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 1292-1302 
    ISSN: 0947-6539
    Keywords: complexes with nitrogen ligands ; ruthenium complexes ; self-assembly ; supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of mono- and dimetallic complexes of rack type containing a dinucleating bis-tridentate ligand and RuII-2,2′:6′,2′-terpyridyl (tpy) sites were synthesised and characterised. The 1H NMR spectra of the dimetallic complexes were correlated to structural features, and the crystal structures of the dimetallic complexes were determined. They provide information about the way in which the central substitutent affects the overall shape of the racks and the relative disposition of the metal centres, measured by the pinching angle of the bis-tridentate ligand and the convergence angle of the ancillary tpy units. The latter demonstrates that a CH3 group yields the least bent complex and indicates how parallel the tpy units are. The dimetallic racks exhibit metal-metal interactions mediated by the bis-tridentate ligands as indicated by electrochemical and spectroscopic methods. The bridging-ligand π* orbital and the dπ metal orbital are stabilised by complexation of a second metal. The results obtained provide guidelines for the design of extended racks bearing several metal centres in a linear arrangement, which also represent potential components of molecular electronic devices.
    Additional Material: 14 Ill.
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  • 3
    ISSN: 0947-6539
    Keywords: bipyridine ligands ; helicates ; kinetics ; mass spectrometry ; self-assembly ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The self-assembly of the pentanuclear double helicates Hh, Ha and He from the corresponding oligobipyridine strands Lh, La and Le and Cu1 ions has been investigated by NMR and electrospray mass spectrometry (ESMS). Where as Hh is assembled rapidly (in less than 20 min), He (about 20 h) and especially Ha (about 60 h) form much more slowly. The rate decreases strongly with increasing steric bulk of the substituents in the 4,4′-positions on the bipyridine units; this indicates that the search processes (wrapping, unwrapping) that lead to the final helicate are strongly hindered by the size of the substituents. The ESMS data give information about the species present in solution under different conditions and allow the formulation of possible formation pathways, which may involve, in particular, helicates of hairpin type.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 977-982 
    ISSN: 1434-1948
    Keywords: Helicates ; Oligobipyridine ligands ; Self-recognition ; NMR titration ; Self-assembly ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
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  • 5
    ISSN: 1434-1948
    Keywords: Self-assembly ; Tetranuclear CuII complex ; [2 × 2] grid-type complex ; Crystal structure ; Magnetic properties ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 3 Ill.
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  • 6
    ISSN: 0570-0833
    Keywords: complexes with nitrogen ligands ; ruthenium compounds ; self-assembly ; supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0570-0833
    Keywords: coordination modes ; multinuclear complexes ; N ligands ; self-assembly ; silver ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 29 (1990), S. 1304-1319 
    ISSN: 0570-0833
    Keywords: Self-assembly ; Information processing ; Molecular information processing ; Molecular recognition ; Supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The selective binding of a substrate by a molecular receptor to form a supramolecular species involves molecular recognition which rests on the molecular information stored in the interacting species. The functions of supermolecules cover recognition, as well as catalysis and transport. In combination with polymolecular organization, they open ways towards molecular and supramolecular devices for information processing and signal generation. The development of such devices requires the design of molecular components performing a given function (e.g., photoactive, electroactive, ionoactive, thermoactive, or chemoactive) and suitable for assembly into an organized array. Light-conversion devices and charge-separation centers have been realized with photoactive cryptates formed by receptors containing photosensitive groups. Eleclroactive and ionoactive devices are required for carrying information via electronic and ionic signals. Redox-active polyolefinic chains, like the “caroviologens”, represent molecular wires for electron transfer through membranes. Push-pull polyolefins possess marked nonlinear optical properties. Tubular mesophases, formed by organized stacking of suitable macro-cyclic components, as well as “chundle”-type structures, based on bundles of chains grafted onto a macrocyclic support, represent approaches to ion channels. Lipophilic macrocyclic units form Langmuir-Blodgett films that may display molecular recognition at the air-water interface. Supramolecular chemistry has relied on more or less preorganized molecular receptors for effecting molecular recognition, catalysis, and transport processes. A step beyond preorganization consists in the design of systems undergoing self-organization, that is, systems capable of spontaneously generating a well-defined supramolecular architecture by self-assembling from their components under a given set of conditions. Several approaches to self-assembling systems have been pursued: the formation of helical metal complexes, the double-stranded helicates, which result from the spontaneous organization of two linear polybipyridine ligands into a double helix by binding of specific metal ions; the generation of mesophases and liquid crystalline polymers of supramolecular nature from complementary components, amounting to macroscopic expression of molecular recognition; the molecular-recognition-directed formation of ordered solid-state structures. Endowing photo-, electro-, and ionoactive components with recognition elements opens perspectives towards the design of programmed molecular and supramolecular systems capable of self-assembly into organized and functional supramolecular devices. Such systems may be able to perform highly selective operations of recognition, reaction, transfer, and structure generation for signal and information processing at the molecular and supramolecular levels.
    Additional Material: 15 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 36 (1997), S. 1294-1296 
    ISSN: 0570-0833
    Keywords: copper ; pseudorotaxanes ; self-assembly ; supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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