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Palladium(II) Complexes of Homologated Ferrocene Phosphanylether and Thioether Ligands

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F17%3A10365521" target="_blank" >RIV/00216208:11310/17:10365521 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/ejic.201701057" target="_blank" >https://doi.org/10.1002/ejic.201701057</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/ejic.201701057" target="_blank" >10.1002/ejic.201701057</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Palladium(II) Complexes of Homologated Ferrocene Phosphanylether and Thioether Ligands

  • Original language description

    The reaction of [1-(diphenylphosphanyl)ferrocenyl]methanol/borane (1:1) with in situ formed N,N,N,N,S-pentamethylisothiouronium iodide and sodium hydride, followed by removal of the borane protecting group with 1,4-diazabicyclo[2.2.2]octane, afforded 1-(diphenylphosphanyl)-1-[(methylthio)methyl]ferrocene (3) as a new, homologated, hybrid phosphanylferrocene ligand. Compound 3 and the congeneric phosphanyl ether 2 were studied as ligands in Pd-II complexes. When treated with [PdCl2(MeCN)2] in a Pd/ligand ratio of 1:1, compound 3 furnished a mixture of two Pd complexes, including the ligand-bridged dimer [{mu(P,S)-3}PdCl2]2 (6), which was structurally characterized. Upon increasing the amount of ligand to 2 equiv., a similar reaction produced the bis(phosphane) complex [PdCl2(3-P)2] (7). Bridge-cleavage reactions of the dipalladium complex [(L-NC)Pd(mu-Cl)]2 {L-NC = 2-[(dimethylamino-N)methyl]phenyl-C-1} with donors 3 and 2 proceeded in a uniform manner to give the corresponding phosphane complexes [(L-NC)PdCl(3-P)] (8) and [(L-NC)PdCl(2-P)] (9). Conversely, removing the Pd-bonded chloride from these complexes with AgClO4 generated the bis(chelate) complex [(L-NC)Pd(3-P-2,S)]ClO4 (10) and the aqua complex [(L-NC)Pd(H2O)(2-P)]ClO4 (11), respectively, both of which could be converted back into their precursors by adding Bu4NCl. The structures of the complexes 6-11 (some in solvated form) were determined by single-crystal X-ray diffraction analysis.

  • 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/GA15-11571S" target="_blank" >GA15-11571S: Unsymmetric phosphinoferrocene donors</a><br>

  • Continuities

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

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    European Journal of Inorganic Chemistry

  • ISSN

    1434-1948

  • e-ISSN

  • Volume of the periodical

    neuveden

  • Issue of the periodical within the volume

    41

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    11

  • Pages from-to

    4850-4860

  • UT code for WoS article

    000414919100006

  • EID of the result in the Scopus database

    2-s2.0-85033452821