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  • Physical Chemistry  (2)
  • Cyclophanes  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 647-658 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Octaethyltetrathiaporphyrin dication, OTP2+, is electrochemically reduced by two successive electron-transfer processes to OPT0. OPT2+ forms intermolecular complexes with a series of π-donors. The association constants of the resulting complexes are controlled by the oxidation potentials of the π-donors and solvent properties. OTP2+ was incorporated into a Nafion membrane cast on a Pt electrode. Formation of OTP2+-π-donor complexes in the polymer membrane was followed by electrochemical and spectroscopic means. The association constants of the OTP2+-π-donor complexes in the Nafion membrane exhibit lower values than a homogeneous phase owing to the high ionic strength in the polyelectrolyte.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The octaethyltetrathiaporphyrin dication, OTP2+, forms 1:1 intermolecular donor-acceptor complexes with NiII-, VIVO- and FeIII-octaethylporphyrins. The association constants of the complexes are governed by the oxidation potential of the metallo-octaethylporphyrins and by secondary electrostatic interactions. Octaethylporphyrin, H2OEP, forms intermolecular complexes with OTP2+. Kinetic analyses of the formation of the various complexes revealed the formation of a primary complex exhibiting the stoichiometry (OTP2+)2(H2OEP). This intermolecular complex transforms into a thermodynamically stabilized intermolecular assembly with a stoichiometry corresponding to (OTP2+)4H2OEP. The activation barrier associated with the conversion of the primary complex to the thermodynamically stabilized assembly is Ea = 16·5 kcal mol-1 (1 kcal = 4·184 kJ). The association constant of the complex (OTP2+)2(H2OEP) is K1 = 1·3 × 1010 M-2 and the equilibrium constant between the two coexisting intermolecular complexes (OTP2+)4(H2OEP) and (OTP2+)2(H2OEP) is K2 = 7·4.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 0009-2940
    Schlagwort(e): Cyclophanes ; Indenyl anions ; Iron complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: [2.2]Metacyclophane can be directly formylated according to the Rieche method to give 4-formyl[2.2]metacyclophane (12) in 44% yield. The synthesis of the [2]metacyclo[2]indenophane 8 from the aldehyde 12 by the pathway previously employed for the corresponding [2.2]paracyclophanes failed due to the harsh conditions of the cyclization step. An alternative synthesis of 8 and its isomer 9 involving the construction of the five-membered ring prior to that of the cyclophane unit succeeded. Compounds 8 and 9 were obtained as an 82:18 mixture, deprotonation of which afforded the anion 10, which shows long-term stability. The 1H-NMR spectrum of this anion does not exhibit a through-space charge transfer due to its structure. The 1H-NMR parameters and molecular mechanics calculations are discussed. Both faces of 10 react in the presence of FeCl2 · 2 THF and a twentyfold excess of LiCp to give a 70:30 mixture of the ferrocene derivatives 7 and 35.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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