Library

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    ISSN: 1434-1948
    Keywords: Photochemistry ; Electrochemistry ; Ruthenium compounds ; α-Diimine complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photophysical, photochemical and redox properties of the title complexes were investigated. Resonance Raman measurements revealed the lowest-energy electronic transition to possess σ→π* character. At low temperatures, long-lived near-IR emission was observed. Irradiation in solution results in homolytic splitting of a Ru-Ru bond as the primary step, followed by secondary reactions of the radical fragments depending on the experimental conditions. (Spectro)electrochemical investigations of the title species proved that the axial [RuCp(CO)2] groups exert a stabilising influence on the corresponding radical cations, while destabilising the corresponding radical anions, compared to the redox behaviour of other ruthenium complexes of this type.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-1948
    Keywords: Spectroelectrochemistry ; Cyclic voltammetry ; Photochemistry ; Copper(II) complexes ; Thiolate complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrochemical and photoredox properties of copper(II) thiopyrazolone Schiff base complexes 1-9 with imine and thiolate coordination, showing variable degrees of tetrahedral distortion, were investigated by means of combined electrochemical and spectroscopic techniques in the temperature range of 193-293 K. The cyclic voltammograms of 1-9 in butyronitrile revealed that the reduction and oxidation paths are strongly dependent on the geometry of the CuN2S2 moiety. Due to the strong delocalization of the singly occupied redox orbital (SOMO) the oxidations and reductions occur in a narrow potential range. The one-electron-reduced 1(r)-9(r) and oxidized 1(o)-9(o) products were electrogenerated and stabilized inside optically transparent thin-layer electrochemical (OTTLE) cells at variable temperatures and could be characterized for the first time by UV/Vis spectroscopy. The reduced formal d10 copper(I) species absorb only weakly in the visible region. The oxidized products 1(o)-9(o) show several strong absorptions in the visible region due to the presence of formal d8 copper(III) species. The spectral information allowed assignment of the initial photoproducts. Irradiations in donor media such as THF or EtOH initially produces 1(r)-9(r). No photoreduction was observed in tBuOH which cannot liberate reducing Hα. The primary oxidized species 1(o)-9(o) were formed in chlorinated acceptor solvents (CHCl3) on UV irradation. Fast relaxation to the ground state prevents the photoredox reactions from CT or LF excited states.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...