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Non-innocent behaviour of ancillary and bridging ligands in homovalent and mixed-valent ruthenium complexes [A2Ru(.mu.L)RuA2]n, A = 2,4-pentanedionato or 2-phenylazopyridine, L2- = 2,5?bis(2-oxidophenyl)pyrazine

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F07%3A00084292" target="_blank" >RIV/61388955:_____/07:00084292 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Non-innocent behaviour of ancillary and bridging ligands in homovalent and mixed-valent ruthenium complexes [A2Ru(.mu.L)RuA2]n, A = 2,4-pentanedionato or 2-phenylazopyridine, L2- = 2,5?bis(2-oxidophenyl)pyrazine

  • Original language description

    Structurally characterised 2,5-bis(2-hydroxyphenyl)pyrazine (H2L) can be partially or fully deprotonated to form the complexes [(acac)2Ru(.mu.-L)Ru(acac)2] [1], acac- = acetylacetonato = 2,4-pentanedionato, [(pap)2Ru(.mu.-L)Ru(pap)2](ClO4)2 [2](ClO4)2, pap = 2-phenylazopyridine, or [(pap)2Ru(.mu.L)Ru](ClO4), [3](ClO4). Several reversible oxidation and reduction processes were observed in each case and were analysed with respect to oxidation state alternatives through EPR and uv-vis-nir spectroelectrochemistry. In relation to previously reported compounds with 2,2/-bipyridine as ancillary ligands the complex redox system [1]n is distinguished by a preference for metal-based electron transfer whereas the systems [2]n and [3]n favour an invariant RuII state.

  • Czech name

    Noninocentní chování pobočných a můstkových ligandů v homovalentních komplexů a komplexů se smíšenou valencí [A2Ru(.mu.-L)RuA2]n, A = 2,4-pentanedionato nebo 2-fenylazopyridin, L2- = 2,5-bis(2-oxidophenyl)pyrazin

  • Czech description

    Strukturně charakterizovaný 2,5-bis(2-hydroxyphenyl)pyrazine (H2L) může být částečně nebo úplně deprotonován a tvořit komplexy [(acac)2Ru(.mu.-L)Ru(acac)2] [1], acac- = acetylacetonato = 2,4-pentanedionato, [(pap)2Ru(.mu.-L)Ru(pap)2](ClO4)2 [2](ClO4)2, pap = 2-phenylazopyridine, nebo [(pap)2Ru(.mu.L)Ru](ClO4), [3](ClO4). Bylo pozorováno několik reversibilních oxidačních a redukčních procesů, jež byly analyzovány z hlediska alternativ oxidačních stavů s použitím EPR a uv-vis-nir spektroelektrochemie. V analogii s dříve popsanými sloučeninami s pobočným ligandem 2,2/-bipyridinem, redox systém [1]n se vyznačuje preferencí pro elektronový přenos na kovu, zatímco systémy [2]n a [3]n upřednostňují neměnný RuII stav.

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

    2007

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    -

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    2411-2418

  • UT code for WoS article

  • EID of the result in the Scopus database