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Synthesis, Reduction Chemistry, and Spectroscopic and Computational Studies of Isomeric Quinolinecarboxaldehyde Triosmium Clusters

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F04%3A00101028" target="_blank" >RIV/61388955:_____/04:00101028 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis, Reduction Chemistry, and Spectroscopic and Computational Studies of Isomeric Quinolinecarboxaldehyde Triosmium Clusters

  • Original language description

    The quinoline derivatives Os-3(CO)(n)(mu(m)-eta(2)-L-H)(mu-H) (L = quinoline-4-carboxaldehyde, n 10, m = 2, 4; n = 9, N-C(8) bound, m = 3, 5; n = 10, N-C(2) bound, m = 2, 6; L = quinoline-3-carboxaldehyde, n = 9, N-C(8) bound, m = 3, 7) are obtained by the reaction of Os-3(CO)(10)(CH3CN)(2) with the quinoline-3-carboxaldehyde or -4-carboxaldehyde ligand followed by photochemical decarbonylation in the case of 5 and 7. The quinoline-4-carboxaldehyde clusters and the free ligand all show reversible 1e(-)reductions, but the electron-deficient 5 shows two separate reversible 1e(-) reductions, the first at much less negative potential than for the previously investigated Os-3(Co)(9)(mu(3)-eta(2) -L-H)(mu-H) (L = phenanthridine, 1; L = 5,6-benzoquinoline, 2), while the free ligand is reduced at a more negative potential than any of the clusters. The spectroscopic properties of the clusters upon electrochemical and chemical reduction have been investigated.

  • Czech name

    Syntéza, redukční chemie, spectroskopické a výpočetní studium isomerických chinolinekarboxaldehydových tříosmiových klastrů

  • Czech description

    Chinolinové deriváty Os-3(CO)(n)(mu(m)-eta(2)-L-H)(mu-H ) (L = chinolin-4-carboxaldehyd, n = 10, m = 2, 4; n = 9, N-C(8 ) vazba, m = 3, 5; n = 10, N-C(2 ) vazba, m = 2, 6; L = chinolin-3-carboxaldehyd, n = 9, N-C(8 ) vazba, m = 3, 7 ) byly získány reakcíOs-3(CO)(10)(CH 3CN)(2) s chinolin-3-carboxaldehydovým nebo -4-carboxaldehydovým ligandem následovanou fotochemickou dekarbonylací v případě 5 a 7. Chinolin-4-carboxaldehydové klastry i volný ligand vykazují reverzibilní 1e(-) redukce, ale elektron-deficitní 5 vykazuje dvě oddělené reverzibilní 1e(-) redukce, první u mnohem méně negativního potenciálu než u dříve vyšetřovaného Os-3(Co)(9)(mu(3)-eta(2 ) -L-H)(mu-H) (L = phenanthridine , 1; L = 5,6-benzochinolin, 2), zatímco volný ligand se redukuje u negativnějšího potenciálu než kterýkoli z klastrů. Byly studovány spectroskopické vlastnosti klastrů po elektrochemické a chemické redukci.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CF - Physical chemistry and theoretical chemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2004

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Organometallics

  • ISSN

    0276-7333

  • e-ISSN

  • Volume of the periodical

    23

  • Issue of the periodical within the volume

    -

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    215-223

  • UT code for WoS article

  • EID of the result in the Scopus database