ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Organic Chemistry  (16)
  • Supramolecular chemistry  (1)
  • molecular devices
  • Self-assembly
  • 1985-1989  (17)
Collection
Keywords
Publisher
Years
Year
  • 11
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nature and Stability of Some Metallic Complexes of Dinucleating Cryptands in Solution II. Polythiamacrotricycles and Related Monocyclic SubunitsThe stability constants of the Cu2+ and Ag+ complexes of the cylindrical macrotricycle 1a (1,7,13,19-tetraaza 4,16-dioxa 10,22,27,32-tetrathiatricyclo[17.5.5.5]tetratriacontane) have been determined by pH-metry, as well as those of the Cu2+, Co2+, Zn2+, Cd2+, Pb2+, and Ag+ complexes of the monocyclic subunit 2a (1,7-dimethyl-1,7-diaza 4,10-dithiacyclododecane), in aqueous solutions (NaClO4) at 25°. In the Cu(II) systems, equilibria were reached slowly, and the results established by pH-metry were confirmed by UV/VIS spectrophotometric studies. The tricycle 1a forms dinuclear cryptates with copper and silver, with overall stability constants log β210 (Cu2-1a)4+ = 18.5, log β21-2 (Cu2-1a(OH)2)2+ = 4.8, log β210(Ag2-1a)2+ = 23.0. Ag+ also forms a mononuclear (Ag-1a)+ complex, with log β110 = 13.1, but no mononuclear species were detected in the Cu-1a system. The absorption spectra of the bis-Cu(II) complexes of 1a and 2a in aqueous medium, MeOH and propylene carbonate (PC) are given, as well as those, in MeOH and PC, of the bis-copper complexes of the related monocycles 3 and 4 (1,7-diaza-4,10,13-trithiacyclopentadecane and 1.10-diaza 4,7,13,16-tetrathiacyclooctadecane, respectively), and tricycle 5 with two benzyl groups in the lateral chains.The complexing properties of the polyoxa- and polythia macrotricycles (Parts I and II of this series) are compared to those of other bis-chelating ligands, the bicyclic bis-tren and the monocyclic bis-dien.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 69 (1986), S. 580-586 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of a series of phosphine-functionalised macrocycles, 1-6, is described. The combination of N-and O-sites with P- and S-sites provides ligands which may bind transition or non-transition metal ions; as a consequence, they give access to dinuclear complexes containing both a Lewis acid and a redox metallic site. Compounds 1,2 and 6 are heterodinucleating ligands capable of binding two dissimilar metals in proximity. Macrocycles 3-5 are homotopic ligands which may form homodinuclear complexes of transition metals.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 72 (1989), S. 1066-1077 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of nine macrocyclic polyamines 2-10 containing pyridine units is described. These compounds are 22- (9), 24- (2-4,6,8,10), or 26- (5, 7) membered hexaaza (2,3,9,10) or octaaza (4-7) macrocycles in which one to four pyridine units are incorporated. Compounds 3,4,9, and 10 are homoditopic ligands, whereas 2 and 5 are heteroditopic and 6-8 multitopic receptors. Compounds 2-10 are potential ligands for metal cations as well as, in their protonated forms, for anions. Protonated macrocycles 2-10 are also potential catalysts for the hydrolysis of nucleotides and polyphosphates.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 72 (1989), S. 1078-1083 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Binding of chloride anion by protonated polyamines was investigated by 35Cl—NMR spectroscopy. The presence of protonated macro(poly)cyclic polyamines caused downfield shifts and significant line broadening of the 53Cl—NMR signals. 35Cl—NMR spectroscopy was used for complex-formation stoichiometry determination and revealed the formation of a binuclear chloride complex with the fully protonated ditopic hexaazamacrocyclic receptor 6. 35Cl—NMR spectroscopy was also applied in competition experiments between Cl— and SO42- and demonstrated that the fully protonated macrocyclic hexaamine 4 forms a strong complex with SO4-2 with 1:1 stoichiometry.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 15
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [fac-Re(bpy) (CO)3Cl] (bpy = 2,2′-bipyridine) is an efficient homogeneous catalyst for the selective and sustained photochemical or electrochemical reduction of CO2 to CO. A quantum yield of 14% and a faradic efficiency of 98% were measured in the presence of excess Cl- ions. The photochemical process took place under visible-light irradiation and consumed a tertiary amine as electron donor. A formato-rhenium complex was isolated in the absence of excess Cl- ions. Substitution by Cl- ion generated free formate, but no CO was detected. Luminescence measurements showed that the tertiary amine quenches the metal-to-ligand charge-transfer excited state of the rhenium complex via a reductive mechanism, with a rate constant of 3.4 × 107M-1S-1. The 19e-complex [Re(bpy) (CO)3X]- produced either photochemically or electrochemically appears to be the active precursor in the CO-generation process. Detailed spectroscopic studies on 13C-enriched carbonyl-rhenium and formato-rhenium complexes derived from 13C-enriched CO2 were performed in order to confirm the origin of the products and to study the exchange of the ligands. A mechanism for the present CO2 photoreduction process is presented; it involves separate pathways for CO and formate generation, in which the [Re(bpy) (CO)3X] complex plays the role of both the photoactive and the catalytic center.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 70 (1987), S. 1-12 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 2,7-diazapyrenium group (DAP2+) combines the features of pyrene, of methylviologen, and of nucleicacid intercalators and may thus present a variety of interesting properties. The cations 1 and 2 and the bis-diazapyrenium species 3 have been synthesized and shown to bind molecular anions like aromatic polycarboxylates, giving rise to pronounced shifts of 1H-NMR signals, modifications of UV/VIS absorption spectra, and quenching of fluorescence. The complexes formed probably have a face-to-face structure, and their stability constants are remarkably high, in particular for the bis-diazapyrenium cation 3 which is susceptible to form intercalative chelate complexes such as 9(log Ks ≈ 3 for 1, up to ca. 7 or more for 3a). Neutral molecules like adenine are also bound, but much less strongly. Visible-light irradiation of Me2DAP2+ (1) in presence of various electron donors, such as EDTA, gives the reduced species Me2DAP+ wich has been characterized by UV/VIS and ESR spectroscopy. The results indicate that Me2DAP2+ (1) functions as a methylviologen analogue, photoactive in visible light. Thus 2,7-diazapyrenium cations are attractive subunits for incorporation into macropolycyclic structures to give photo- and electroactive receptor molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 17
    ISSN: 0570-0833
    Keywords: Supramolecular chemistry ; Nobel lecture ; Macrocycles ; Molecular recognition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Supramolecular chemistry is the chemistry of the intermolecular bond, covering the structures and functions of the entities formed by association of two or more chemical species. Molecular recognition in the supermolecules formed by receptor-substrate binding rests on the principles of molecular complementarity, as found in spherical and tetrahedral recognition, linear recognition by coreceptors, metalloreceptors, amphiphilic receptors, and anion coordination. Supramolecular catalysis by receptors bearing reactive groups effects bond cleavage reactions as well as synthetic bond formation via cocatalysis. Lipophilic receptor molecules act as selective carriers for various substrates and make it possible to set up coupled transport processes linked to electron and proton gradients or to light. Whereas endoreceptors bind substrates in molecular cavities by convergent interactions, exoreceptors rely on interactions between the surfaces of the receptor and the substrate; thus new types of receptors, such as the metallonucleates, may be designed. In combination with polymolecular assemblies, receptors, carriers, and catalysts may lead to molecular and supramolecular devices, defined as structurally organized and functionally integrated chemical systems built on supramolecular architectures. Their recognition, transfer, and transformation features are analyzed specifically from the point of view of molecular devices that would operate via photons, electrons, or ions, thus defining fields of molecular photonics, electronics, and ionics. Introduction of photosensitive groups yields photoactive receptors for the design of light-conversion and charge-separation centers. Redox-active polyolefinic chains represent molecular wires for electron transfer through membranes. Tubular mesophases formed by stacking of suitable macrocyclic receptors may lead to ion channels. Molecular self-assembling occurs with acyclic ligands that form complexes of double-helical structure. Such developments in molecular and supramolecular design and engineering open perspectives towards the realization of molecular photonic, electronic, and ionic devices that would perform highly selective recognition, reaction, and transfer operations for signal and information processing at the molecular level.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...