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Alternative syntheses and X-ray diffraction analyses of the parent tricarbaborane compounds [nido-7,8,9-C(3)B(8)H(11)](-), [nido-7,8,10-C(3)B(8)H(11)](-) and [1-(eta(5)-C(5)H(5))-closo-1,2,4,10-FeC(3)B(8)H(11)]

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F11%3A39892396" target="_blank" >RIV/00216275:25310/11:39892396 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388980:_____/11:00366250

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2011.04.021" target="_blank" >http://dx.doi.org/10.1016/j.jorganchem.2011.04.021</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2011.04.021" target="_blank" >10.1016/j.jorganchem.2011.04.021</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Alternative syntheses and X-ray diffraction analyses of the parent tricarbaborane compounds [nido-7,8,9-C(3)B(8)H(11)](-), [nido-7,8,10-C(3)B(8)H(11)](-) and [1-(eta(5)-C(5)H(5))-closo-1,2,4,10-FeC(3)B(8)H(11)]

  • Original language description

    Reaction of the neutral tricarbaborane nido-7,8,9-C(3)B(8)H(12) (1) with triethylamine in CH(2)Cl(2) led to quantitative deprotonation and isolation of the corresponding Et(3)NH(+) salt of the [nido-7,8,9-C(3)B(8)H(11)](-) anion (2). This was converted into PSH(+) and Me(4)N(+) salts via metathetic cation exchange. Heating of the solid Me(4)N(+)[7,8,9-C(3)B(8)H(11)](-) in mineral oil at 350 degrees C for 2 h resulted in thermal rearrangement and isolation of the cage isomeric compound Me(4)N(+)[7,8,10-C(3)B(8)H(11)](-). Finally, compound 1 was directly complexed via reaction with [CpFe(CO)(2)](2) (Cp = eta(5)-C(5)H(5)) to generate the ferratricarbollide sandwich [1-Cp-closo-1,2,4, 10-FeC(3)B(8)H(11)] (4) in 60% yield. The structures of all the genericcompounds of tricarbollide chemistry, 1 (PSH(+) salt), 2 (MePPh(3)(+)salt), and 4, were established unambiguously by an X-ray diffraction analysis.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CA - Inorganic 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

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Organometallic Chemistry

  • ISSN

    0022-328X

  • e-ISSN

  • Volume of the periodical

    696

  • Issue of the periodical within the volume

    14

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    4

  • Pages from-to

    2742-2745

  • UT code for WoS article

    000291246800007

  • EID of the result in the Scopus database