All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Indenyl Compounds with Constrained Hapticity: The Effect of Strong Intramolecular Coordination

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F16%3A39901717" target="_blank" >RIV/00216275:25310/16:39901717 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1002/ejic.201601029" target="_blank" >http://dx.doi.org/10.1002/ejic.201601029</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/ejic.201601029" target="_blank" >10.1002/ejic.201601029</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Indenyl Compounds with Constrained Hapticity: The Effect of Strong Intramolecular Coordination

  • Original language description

    A series of cyclopentadienyl and indenyl molybdenum(II) compounds with intramolecularly coordinated pyridine arms, including scorpionate-like species bearing two irreversibly coordinated arms on the indenyl core, were synthesized and characterized. All presented structural types were confirmed by X-ray diffraction analysis. Owing to the strong nucleophilicity of pyridine, the intramolecular interaction was found to be considerably stronger than that in analogous species bearing tertiary amines in the side chain. Although the starting compounds for the syntheses were isostructural, the reaction outcomes differed considerably. The cyclopentadienyl precursor gave a pentacoordinate ?5:?N-compound, whereas the indenyl analogue produced a hexacoordinate species with the unprecedented ?3:?N-coordination mode of the indenyl ligand and thus represents an unusual example of the so-called indenyl effect. The unusually high stability of the ?3:?N-coordination compounds toward haptotropic rearrangement was clarified by theoretical calculations. As the strong intramolecular interaction prevented rotation of the indenyl moiety, it could not reach the conformation suitable for the ?3 to ?5 rearrangement. As a result, the low hapticity was effectively locked.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • 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

    33

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    15

  • Pages from-to

    5250-5264

  • UT code for WoS article

    000388494000010

  • EID of the result in the Scopus database