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Assessing the influence of phosphine substituents on the catalytic properties of self-stabilised digold(I) complexes with supporting ferrocene phosphinonitrile ligands

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F19%3A10396149" target="_blank" >RIV/00216208:11310/19:10396149 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=HuNNgEpaaW" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=HuNNgEpaaW</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c9nj02555c" target="_blank" >10.1039/c9nj02555c</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Assessing the influence of phosphine substituents on the catalytic properties of self-stabilised digold(I) complexes with supporting ferrocene phosphinonitrile ligands

  • Original language description

    Gold(i) phosphine complexes are often used in catalysis, but the role of their auxiliary ligands still remains poorly understood. Thus, building on our previous research, we prepared a series of Au(I) complexes [Au-2(mu-R(2)PfcCN)(2)][SbF6](2) (fc = ferrocene-1,1&apos;-diyl) to assess the effect of phosphine groups PR2 on the catalytic properties of these highly catalytically active, dimeric compounds. Catalytic testing in Au-mediated cyclisation of N-propargyl amides to 2-substituted 5-methyleneoxazolines showed that weaker donating phosphines gave rise to more active, albeit partly destabilised, catalysts. Nevertheless, thanks to their self-stabilisation by reversible nitrile coordination, [Au-2(mu-R(2)PfcCN)(2)](+) cations readily converted into catalytically active species (by dissociation) and, in addition, remained catalytically active even at very low metal loadings. The experimental results were supported by the trends in (1)J(PSe) coupling constants for R2P(Se)fcCN as a measure of ligand basicity, and by DFT calculations.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/GA17-02495S" target="_blank" >GA17-02495S: Coordination behaviour and synthetic transformations of phosphinoferrocene isonitriles and alkynes</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    New Journal of Chemistry

  • ISSN

    1144-0546

  • e-ISSN

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    28

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    5

  • Pages from-to

    11258-11262

  • UT code for WoS article

    000475699900026

  • EID of the result in the Scopus database

    2-s2.0-85069512689