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  • General Chemistry  (2)
  • Earth Resources and Remote Sensing
  • Fisheries
  • Polymer and Materials Science
  • 1985-1989  (3)
  • 1
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: These studies compare the voltammetric behavior of solutions and adsorbed layers of the following unsaturated alcohols: benzyl alcohol (BZA), 4-pyridylcarbinol (4PC), allyl alcohol (AA), propargyl alcohol (PGA), cis-2-butene-1,4-diol (CBED), and 2-butyne-1,4-diol (BYD). They were undertaken for well-characterized Pt(111) electrode surfaces which were either annealed in an ultrahigh vacuum (UHV) or electrochemically cycled, as well as for annealed (UHV) Pt(poly). Electrochemical oxidation of BZA, AA, PGA, CBED, and BYD in aqueous fluoride electrolyte proceeds in two stages: first the alcohol moiety is oxidized to CO2 (0.4 V), followed by oxidation of the resulting adsorbed hydrocarbon (alkene, alkyne, or phenyl, 1.0 V); 4PC is relatively inert. The alcohol moiety in 4PC, which is located opposite the pyridine ring from the surface, does not undergo oxidation at an appreciable rate. in fact, 4PC effectively passivates the surface and poisons the electrochemical activity. Electrochemical cycling of the annealed Pt(111) single-crystal surface greatly increases the oxidation rates of the aliphatic alcohols and, to a lesser extent, increases the oxidation rate of BZA. The oxidation rate enhancement is somewhat smaller if the electrode is electrochemically cycled in the presence of the alcohol. The majority of the difference effected by cycling can be observed after only one cycle. Voltammetry on polycrystalline Pt surfaces resembles that on cycled Pt(111) surfaces for PGA and AA, but resembles that on cycled Pt(111) surfaces for PGA and AA, but resembles that on annealed Pt(111) more closely for the diols CBED and BYD.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 97 (1985), S. 837-853 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ein Komplex, der zwei oder mehr paramagnetische übergangsmetall-Ionen enthält, kann völlig andere magnetische Eigenschaften haben als Einkernkomplexe dieser Ionen. Die Eigenschaften von Zweikernkomplexen hängen von Art und Stärke der Metall-Metall-Wechselwirkungen über die verbrückenden Liganden ab. Weisen beide Ionen je ein ungepaartes Elektron auf (z. B. Cu2+-Ionen), dann ist der energetische Grundzustand des Moleküls entweder ein Spin-Singulett oder ein Spin-Triplett. Im ersten Fall spricht man von antiferromagnetischer, im zweiten von ferromagnetischer Wechselwirkung. Art und Stärke der Wechselwirkung können durch die Wahl der Metall-Ionen sowie der verbrückenden und der terminalen Liganden und damit durch die Symmetrie und die Delokalisierung der metallzentrierten Orbitale, die von den ungepaarten Elektronen besetzt sind (magnetische Orbitale), gesteuert werden. Dies gelang zuerst bei einem rein ferromagnetischen Cu2+VO2+-Komplex. Die gleiche Strategie konnte zur Herstellung molekularer Ferromagnete genutzt werden, die eine der größten Herausforderungen auf dem Feld molekularer Werkstoffe ist. Man kann das Ausmaß der Wechselwirkung in einer vorgegebenen verbrückten Struktureinheit durch Variation der terminalen Liganden, die die Rolle von „Justierschrauben“ übernehmen, genau abstimmen. Durch die sorgfältige Wahl sowohl der verbrückenden als auch der terminalen Liganden kann eine sehr starke antiferromagnetische Wechselwirkung erreicht werden, sogar im Falle weit voneinander entfernter Metall-Ionen. Einige schwefelhaltige Brücken sind dafür besonders geeignet.
    Additional Material: 29 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 834-850 
    ISSN: 0570-0833
    Keywords: Dinuclear complexes ; Complexes ; Magnetic properties ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When two paramagnetic transition metal ions are present in the same molecular entity, the magnetic properties can be totally different from the sum of the magnetic properties of each ion surrounded by its nearest neighbors. These new properties depend on the nature and the magnitude of the interaction between the metal ions through the bridging ligands. If both ions have an unpaired electron (e.g. Cu2+ ions), then the molecular state of lowest energy is either a spin singlet or a spin triplet. In the former case, the interaction is said to be antiferromagnetic, in the latter case ferromagnetic. The nature and the order of magnitude of the interaction can be engineered by judiciously choosing the interacting metal ions and the bridging and terminal ligands, and, thus, by the symmetry and the delocalization of the orbitals centered on the metal ions and occupied by the unpaired electrons (magnetic orbitals). The first success in this “molecular engineering” of bimetallic compounds was in the synthesis of a Cu2+VO2+ heterobimetallic complex in which the interaction is purely ferro-magnetic. The same strategy could be utilized for designing molecular ferromagnets, one of the major challenges in the area of molecular materials. Another striking result is the possibility of tuning the magnitude of the interaction through a given bridging network by modifying the nature of the terminal ligands, which, in some way, play the role of “adjusting screws”. By careful selection of the bridging and terminal ligands, a very large antiferro-magnetic interaction can be achieved, even if the metal ions are far away from each other. Some sulfur-containing bridges are especially suitable in this respect.
    Additional Material: 29 Ill.
    Type of Medium: Electronic Resource
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