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A combined experimental and DFT study on the complexation of the hydrazinium cation with a hexaarylbenzene - based receptor

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    SYSNO ASEP0364678
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleA combined experimental and DFT study on the complexation of the hydrazinium cation with a hexaarylbenzene - based receptor
    Author(s) Makrlík, E. (CZ)
    Toman, Petr (UMCH-V) RID, ORCID
    Vaňura, P. (CZ)
    Rathore, R. (US)
    Source TitleActa Chimica Slovenica. - : Slovensko Kemijsko Drustvo - ISSN 1318-0207
    Roč. 58, č. 3 (2011), s. 611-615
    Number of pages5 s.
    Languageeng - English
    CountrySI - Slovenia
    Keywordshexaarylbenzene – based receptor ; N2H+ 5 cation ; complexation
    Subject RIVBM - Solid Matter Physics ; Magnetism
    R&D ProjectsGAP205/10/2280 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000295872200032
    AnnotationFrom extraction experiments and γ-activity measurements, the exchange extraction constant corresponding to the equilibrium N2H+5 (aq) + 1.Cs+(nb) – 1.N2H+5 (nb) + Cs+(aq) taking place in the two–phase water–nitrobenzene system (1 =hexaarylbenzene–based receptor; aq = aqueous phase, nb = nitrobenzene phase) was evaluated as log Kex (N2H+5, 1.Cs+)= –1.2. Further, the stability constant of the complex 1.N2H+5 in nitrobenzene saturated with water was calculated: log βnb (1.N2H+5) = 5.6. Using quantum chemical calculations, the most probable structure of this complex was solved. In this complex, the cation N2H+5 synergistically interacts with the polar ethereal oxygen fence and with the central hydrophobic benzene bottom via cation–π interaction. Finally, the calculated binding energy of the resulting complex is –270.5 kJ/mol, confirming the relatively high stability of the considered cationic complex species.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2012
    Electronic addresshttp://acta.chem-soc.si/58/58-3-611.pdf
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