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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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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