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Oxidations of N-coordinated Arsinidene and Stibinidene by Substituted Quinones: A Remarkable Follow-Up Reactivity

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F23%3A39920980" target="_blank" >RIV/00216275:25310/23:39920980 - isvavai.cz</a>

  • Result on the web

    <a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cplu.202300018" target="_blank" >https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cplu.202300018</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/cplu.202300018" target="_blank" >10.1002/cplu.202300018</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Oxidations of N-coordinated Arsinidene and Stibinidene by Substituted Quinones: A Remarkable Follow-Up Reactivity

  • Original language description

    The reactivity of pnictinidenes [2-(DippN=CH)-6-(DippNHCH(2))C6H3]E (where E=As (1) or Sb (2)) toward substituted ortho- and para-quinones is reported. The central pnictogen atom is easily oxidized by ortho-quinones closing five-membered EO2C2 ring. The oxidized antimony derivatives are stable species, while in the case of arsenic compounds the hydrogen of the pendant amino NHCH2 group cleaves one newly formed As-O bonds leading to the closure of a new azaarsole ring. Furthermore, a heating of these arsenic heterocycles resulted in a C-H bond activation at the NCH2 group involved in this heterocycle followed by a reductive elimination of corresponding catechols and arsinidene [2,6-(DippN=CH)C6H3]As. Using of para-quinones, resulted in the oxidation of the central atom with a concomitant hydrogen migration from NHCH2 group even in the case of the antimony derivatives. The reductive elimination of hydroquinones is in this case feasible for all compounds. Studied compounds were characterized by multi-nuclear NMR, IR and Raman spectroscopy and single-crystal X-ray diffraction analysis. The theoretical study focusing the key compounds and reactions is also included.

  • 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/GA21-02964S" target="_blank" >GA21-02964S: Nitrogen Ligands for Main-Group Elements - Becoming Bulkier, More Conjugated and Guilty</a><br>

  • Continuities

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

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    ChemPlusChem

  • ISSN

    2192-6506

  • e-ISSN

    2192-6506

  • Volume of the periodical

    88

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    9

  • Pages from-to

    "e202300018"

  • UT code for WoS article

    000935181600001

  • EID of the result in the Scopus database

    2-s2.0-85148609829