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Catalytic performance of Metal-Organic-Frameworks vs.extra-large porezeolite UTL in condensation reactions

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    SYSNO ASEP0421160
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleCatalytic performance of Metal-Organic-Frameworks vs.extra-large porezeolite UTL in condensation reactions
    Author(s) Shamzhy, Mariya (UFCH-W) RID, ORCID
    Opanasenko, Maksym (UFCH-W) RID, ORCID
    Shvets, O. V. (UA)
    Čejka, Jiří (UFCH-W) RID, ORCID, SAI
    Source TitleFrontiers in Chemistry. - : Frontiers Media - ISSN 2296-2646
    Roč. 1, AUG 2013 (2013), s. 1-11
    Number of pages11 s.
    Publication formOnline - E
    Languageeng - English
    CountryUS - United States
    Keywordscondensation reactions ; MOFs ; zeolites
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGBP106/12/G015 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUFCH-W - RVO:61388955
    DOI10.3389/fchem.2013.00011
    AnnotationCatalytic behavior of isomorphously substituted B-, Al-, Ga-, and Fe-containing extra-large pore UTL zeolites was investigated in Knoevenagel condensation involving aldehydes, Pechmann condensation of 1-naphthol with ethylacetoacetate, and Prins reaction of β-pinene with formaldehyde and compared with large-pore aluminosilicate zeolite beta and representative Metal-Organic-Frameworks Cu3(BTC)2 and Fe(BTC). The yield of the target product over the investigated catalysts in Knoevenagel condensation increases in the following sequence: (Al)beta < (Al)UTL < (Ga)UTL < (Fe)UTL < Fe(BTC) < (B)UTL < Cu3(BTC)2 being mainly related to the improving selectivity with decreasing strength of active sites of the individual catalysts. The catalytic performance of Fe(BTC), containing the highest concentration of Lewis acid sites of the appropriate strength is superior over large-pore zeolite (Al)beta and B-, Al-, Ga-, Fe-substituted extra-large pore zeolites UTL in Prins reaction of β-pinene with formaldehyde and Pechmann condensation of 1-naphthol with ethylacetoacetate.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2014
Number of the records: 1  

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