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Highly substituted zirconium and hafnium cyclopentadienyl bifunctional ?-diketiminate complexes ? Synthesis, structure, and catalytic activity towards ethylene polymerization

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F15%3A00443392" target="_blank" >RIV/61388955:_____/15:00443392 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2015.03.014" target="_blank" >http://dx.doi.org/10.1016/j.jorganchem.2015.03.014</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2015.03.014" target="_blank" >10.1016/j.jorganchem.2015.03.014</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Highly substituted zirconium and hafnium cyclopentadienyl bifunctional ?-diketiminate complexes ? Synthesis, structure, and catalytic activity towards ethylene polymerization

  • Original language description

    A series of tetramethyl-(Cp) and pentamethylcyclopentadienyl (Cp*) metal complexes (?5-C5Me4R)ZrCl2LCO (R = H(1), Me(2)) and (?5-C5Me4R)HfCl2LCO (R = H(3), Me(4)) where LCO is a bifunctional ?-diketiminate ligand [2-(MeO)?C6H4)]NC(Me)CHC(Me)N[2-(MeO)?C6H4)] (LCO) were prepared from corresponding tetramethyl- and (pentamethylcyclopentadienyl)metal trichlorides and the lithium precursor LiLCO. All complexes were characterized by their melting point, elemental analysis, 1H and 13C NMR spectroscopy, IR spectroscopy. In addition their solid-state structures were determined by X-ray diffraction techniques. In all cases, a pseudo-tetragonal pyramidal coordination environment of the metal centre with cyclopentadienyl ligand on the top and nearly isobidentatelybonded nitrogen atoms of the chelating LCO ligand in an open ?5-fashion was observed. The oxygen atoms positioned at the diketiminate periphery remained uncoordinated to transition metal in the solid phase as well as in solution. Besides

  • Czech name

  • Czech description

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

    <a href="/en/project/GAP106%2F10%2F0924" target="_blank" >GAP106/10/0924: The electron deficient transition metal complexes containing bifunctional beta-diketiminate and cyclopentadienyl ligands ? design of new catalysts.</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • 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

    786

  • Issue of the periodical within the volume

    JUN 2015

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    10

  • Pages from-to

    71-80

  • UT code for WoS article

    000354562200010

  • EID of the result in the Scopus database

    2-s2.0-84927589212