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Experimental evidence, stability, and the most probable structure of protonated p-tert-butylcalix[4]arenetetrakis (N,N-dimethylacetamide)

  1. 1.
    SYSNO ASEP0330562
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleExperimental evidence, stability, and the most probable structure of protonated p-tert-butylcalix[4]arenetetrakis (N,N-dimethylacetamide)
    Author(s) Makrlík, E. (CZ)
    Dybal, Jiří (UMCH-V) RID, ORCID
    Budka, J. (CZ)
    Vaňura, P. (CZ)
    Source TitleMonatshefte fur Chemie. - : Springer - ISSN 0026-9247
    Roč. 140, č. 10 (2009), s. 1155-1158
    Number of pages4 s.
    Languageeng - English
    CountryAT - Austria
    Keywordscalixarenes ; macrocycles ; protonation
    Subject RIVCD - Macromolecular Chemistry
    R&D Projects1ET400500402 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000270185100005
    DOI10.1007/s00706-009-0165-z
    AnnotationFrom extraction experiments and gamma-activity measurements, the extraction constant corresponding to the equilibrium H3O+(aq) + 1.Na+(nb) equil. 1.H3O+ (nb) + Na+ (aq) taking place in the two-phase water-nitrobenzene system (1: p-tert-butylcalix[4] arenetetrakis(N,N-dimethylacetamide)) was evaluated as -0.1 +/- 0.1. By using quantum mechanical DFT calculations, the most probable structure of the 1.H3O+ cationic complex species was derived.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2010
Number of the records: 1  

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