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Tetrafluoro-4-pyridyl substituted cyclopentadienyl molybdenum(II) compounds

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F14%3A10283566" target="_blank" >RIV/00216208:11150/14:10283566 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216275:25310/14:39896485

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2013.10.034" target="_blank" >http://dx.doi.org/10.1016/j.jorganchem.2013.10.034</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2013.10.034" target="_blank" >10.1016/j.jorganchem.2013.10.034</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tetrafluoro-4-pyridyl substituted cyclopentadienyl molybdenum(II) compounds

  • Original language description

    The allyl molybdenum(II) complex bearing tetrafluoro-4-pyridyl substituted cyclopentadienyl ligand, [(?3-C3H5){?5-C5H3(C5F4N)}Mo(CO)2], was synthesized and characterized by analytical and spectroscopic methods. This compound was found to be suitable precursor for complexes of the type [{?5-C5H4(C5F4N)}Mo(CO)2(NNL)][BF4] where NNL is N,N-chelating ligand. The biological study has shown that these complexes are cytotoxic active toward human leukemia cells MOLT-4. The cytotoxicity strongly depends on nature of the coordinated N,N-chelating ligand. The compounds bearing 1,10-phenanthroline (phen) and 2,2'-biquinoline (bq) are only medium active while the complexes with 4,7-diphenyl-1,10-phenanthroline (4,7-Ph2-phen) and 5-amino-1,10-phenanthroline (5-NH2-phen) show considerably higher activity than cisplatin. This study further describe the X-ray structures of [(?3-C3H5){?5-C5H4(C5F4N)}Mo(CO)2], [(?3-C3H5){?5-C5H3(1,3-C5F4N)2}Mo(CO)2], [{?5-C5H4(C5F4N)}Mo(CO)2(phen)][BF4] and [{?5-C5H4(C5F

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • 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

    749

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    7

  • Pages from-to

    387-393

  • UT code for WoS article

    000327939000056

  • EID of the result in the Scopus database