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  • 11
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1041-1047 
    ISSN: 0009-2940
    Keywords: Biomimetic catalysis ; Oxygen activation ; Schiff base complexes ; Complexes of Mn, Fe, and Co ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The metal complexes (E,E)-[{diethyl 2,2′-[1,2-phenylenebis(iminomethylidyne)]bis[3-oxobutanoato]}(2-)-N,N′,O3,O3′]manganese (Mn1a), [3,3′]-[1,2-phenylenebis(iminomethylidyne)bis(2,4-pentanedionato)(2-)-N,N′,O2,O2′]manganese (Mn1b), and (Z,Z)-[diethyl 3,3′-(1,2-phenylenediimino)bis(2-cyano-2-propenoato)](2-)-N3,N3′,O1,O1′]manganese (Mn1c) were sythesised and the oxygenation of these complexes was investigated by gas volumetry. All complexes except Mn1c are able to take up oxygen but with different magnitudes. The catalytic activity of the Mn, Co, and Fe complexes of the ligands 1a and 1c and (E,E)-[{diethyl 2,2′-[1,2-ethylenebis(iminomethylidyne)]bis[3-oxobutanoato]} (2-)N,N′,O3,O3′] iron (Fe1d) and [diethyl (all-E)-5,14-dihydro-6,17-dimethyldibenzo[b,i][1,4,8,11]tetraazacyclotetradecine-7,16-dicarboxylato)(2-)-N5,N9,N14,N18]iron (Fe2a) has been compared with respect to the oxidation of hydroquinone by molecular oxygen. The results are interpreted with the aid of electrochemical properties, Lewis acidities, and other relevant factors. However, no simple relationship between the catalytic activity and the other factors could be found.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 503-514 
    ISSN: 0009-2940
    Keywords: Cu, Ni, Co, Fe complexes ; Template synthesis ; Tetraaza macrocycles ; X-ray structure, H bridges, ID-coordination polymers ; Electrochemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Unsymmetrically Bridged [N4] Macrocycles: Synthesis, Structure and Redox BehaviourMetal complexes M-5a (M = Cu, Ni, Co, Fe, and I-Fe11) of 6,13-Di(ethoxycarbonyl)-7,12-dimethyl-benzo[b]-1,4,8,11-tetraaza-cyclotetradeca-2,5,7,11,13-pentaene and the free ligand H2-5a have been synthesized. The crystals of Cu-5a · H2O and Ni-5a · H2O consist of planar complex molecules which are linked by H bridges between the water molecules and the peripheric ester groups to give 1D chains. The average M-N distances are equal for both complexes (Cu 1.928, Ni 1.924 Å), being unexpectedly large for the nickel complex. The redox properties of all the new compounds as well as some acetyl derivatives M-5b have been examined by cyclic voltammetry and compared with those of the previously reported symmetrically phenylene (M-4) and ethylene (M-6) bridged derivatives. All complexes give a reversible single electron reduction which clearly shows the increasing electron density around the central atom in the order M-4 〈 M-5 〈 M-6. Like the carbonyl substituted tetraazaannulenes M-4 the copper complexes Cu-5 give two, the cobalt complexes Co-5 three, and the iron complex Fe-5a probably four reversible single electron oxidations. They can be attributed to the species [MIIIL-II]+, [MIILo]2+, [MIIILo]3+, and [FeIVLo]4+ with Lo being a “non innocent” neutral 1,2-quinodiimine ligand. Very surprisingly, since in contrast to Ni-4 and Ni-6, the nickel complexes Ni-5 gave no reversible oxidation.
    Additional Material: 4 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 68 (1996), S. 287-289 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure Reactivity Correlations in Coordinatively Unsaturated Chelate Complexes. II. Effect of the Ligand Substituents on the Acceptor Tendency of Planar Copper ComplexesThe effects of the ligand substituents R, R1, R2 and R′ on the acceptor tendency of the planar copper(II) chelates I, II and III are investigated by photometric measurements of equilibrium constants (and, in part, thermodynamic data) for the base adduct formation with pyridine. All of the complexes I and II but not the macrocycles III form mono adducts in solution. The Vis-spectra of known and some new complexes in benzene and pyridine resp. are discussed. The redox properties for some complexes are characterized by voltammetric data. The results are compared with those for the corresponding nickel chelates. The ligand effects on the acceptor tendency against bases or electrons are considerably smaller in the case of copper complexes than for the nickel complexes.
    Notes: Die Effekte der Ligandsubstituenten R, R1, R2 und R′ auf die Akzeptortendenz planarer Kupferchelate I, II und III wurden durch photometrische Messung von Gleichgewichtskonstanten (und, z. T., thermodynamischen Daten) für die Adduktbildung mit Pyridin untersucht. Die Vis-Spektren für bekannte und einige neue Komplexe in Benzen und Pyridin werden diskutiert. Alle Komplexe I und II, aber nicht die Makrozyklen III, bilden in Lösung Monoaddukte. Die Redoxeigenschaften einiger Komplexe werden durch voltammetrische Daten charakterisiert. Die Ergebnisse werden mit jenen für die entsprechenden Nickelchelate verglichen. Die Ligandeffekte auf die Akzeptortendenz gegenüber Basen oder Elektronen sind im Fall der Kupferkomplexe beträchtlich geringer als für die Nickelkomplexe.
    Additional Material: 3 Ill.
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