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Introducing novel redox-active bis(phenolate) N-heterocyclic carbene proligands: investigation of their coordination to Fe(II)/Fe(III) and their catalytic activity in transfer hydrogenation of carbonyl compounds

  1. 1.
    SYSNO ASEP0587134
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleIntroducing novel redox-active bis(phenolate) N-heterocyclic carbene proligands: investigation of their coordination to Fe(II)/Fe(III) and their catalytic activity in transfer hydrogenation of carbonyl compounds
    Author(s) Neshat, A. (IR)
    Mobarakeh, A.M. (IR)
    Yousefshahi, M.R. (IR)
    Varmaghani, F. (IR)
    Dušek, Michal (FZU-D) RID, ORCID, SAI
    Eigner, Václav (FZU-D) RID, ORCID
    Kučeráková, Monika (FZU-D) RID, ORCID
    Number of authors7
    Source TitleACS Omega. - : American Chemical Society - ISSN 2470-1343
    Roč. 9, č. 23 (2024), s. 25135-25145
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    Keywordscarbene bisphenolate ligands ; pincer proligands ; cyclization ; crystal structure ; X-ray crystallography
    Subject RIVBM - Solid Matter Physics ; Magnetism
    OECD categoryCondensed matter physics (including formerly solid state physics, supercond.)
    R&D ProjectsEH22_008/0004594 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportFZU-D - RVO:68378271
    UT WOS001237250300001
    EID SCOPUS85195054111
    DOI https://doi.org/10.1021/acsomega.4c02602
    AnnotationA simple and efficient procedure for synthesizing novel pincer-type tridentate N-heterocyclic carbene bisphenolate ligands is reported. The synthesis of pincer proligands with N,N′-disubstituted imidazoline core, 5 and 6, was carried out via triethylorthoformate-promoted cyclization of either N,N′-bis(2-hydroxy-3,5-di-tert-butylphenyl)cyclohexanediamine, 3, or N,N′-bis(2-hydroxyphenyl)cyclohexanediamine, 4, in the presence of concentrated hydrochloric acid. Cyclic voltammograms of the ligands revealed ligand-centered redox activity, indicating the noninnocent nature of the ligands.
    WorkplaceInstitute of Physics
    ContactKristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
    Year of Publishing2025
    Electronic addresshttps://hdl.handle.net/11104/0354409
Number of the records: 1  

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