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Imidazolium Based Fluorous N-Heterocyclic Carbenes as Effective and Recyclable Organocatalysts for Redox Esterification

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    SYSNO ASEP0524181
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleImidazolium Based Fluorous N-Heterocyclic Carbenes as Effective and Recyclable Organocatalysts for Redox Esterification
    Author(s) Červenková Šťastná, Lucie (UCHP-M) RID, ORCID, SAI
    Bílková, Veronika (UCHP-M) SAI
    Cézová, T. (CZ)
    Cuřínová, Petra (UCHP-M) RID, SAI, ORCID
    Karban, Jindřich (UCHP-M) RID, ORCID, SAI
    Čermák, Jan (UCHP-M) RID, ORCID, SAI
    Krupková, Alena (UCHP-M) RID, ORCID, SAI
    Strašák, Tomáš (UCHP-M) RID, ORCID, SAI
    Source TitleEuropean Journal of Organic Chemistry - ISSN 1434-193X
    Roč. 2020, č. 24 (2020), s. 3591-3598
    Number of pages9 s.
    Languageeng - English
    CountryDE - Germany
    Keywordsfluorous ionic liquids ; N-heterocyclic carbenes ; organocatalysis
    Subject RIVCC - Organic Chemistry
    OECD categoryOrganic chemistry
    Method of publishingLimited access
    Institutional supportUCHP-M - RVO:67985858
    UT WOS000538770500001
    EID SCOPUS85086030389
    DOI10.1002/ejoc.202000273
    AnnotationA series of new highly fluorophilic ionic liquids ( f > 110) was synthetized from 3‑iodopropyltris(3,3,4,4,5,5,6,6,7,7,8,8,8‐tridecafluorooctyl)silane and N‐alkyl imidazoles, followed by anion exchange. N‐heterocyclic carbenes generated in situ from obtained imidazolium salts were employed to catalyze redox esterification ( umpolung ) of cinnamaldehyde with alcohols. The most effective N‐methyl derivative with iodide as a counter anion was studied in detail with respect to the optimization of reaction conditions, substrate scope and recyclability. Recovery of the precatalyst was achieved using either fluorous extraction or performing the reaction in suitable fluorous biphase system with direct recycling of the fluorinated precatalyst phase. For both tested options, the catalytic activity did not significantly decrease within 5 subsequent cycles. The redox esterification was shown to proceed also in supercritical carbon dioxide (scCO 2 ) as an alternative solvent where the activity of the fluorinated catalyst was also superior to the nonfluorinated model, while retaining the benefit of easy recycling.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2021
    Electronic addresshttp://hdl.handle.net/11104/0309759
Number of the records: 1  

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