Počet záznamů: 1  

The formation of quasi-alicyclic rings in alkyl-aromatic compounds

  1. 1.
    SYSNO ASEP0482185
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevThe formation of quasi-alicyclic rings in alkyl-aromatic compounds
    Tvůrce(i) Straka, Pavel (USMH-B) RID, ORCID, SAI
    Buryan, P. (CZ)
    Bičáková, Olga (USMH-B) RID, ORCID, SAI
    Zdroj.dok.Journal of Molecular Structure. - : Elsevier - ISSN 0022-2860
    Roč. 1154, Feb 15 (2018), s. 455-462
    Poč.str.8 s.
    Forma vydáníTištěná - P
    Jazyk dok.eng - angličtina
    Země vyd.NL - Nizozemsko
    Klíč. slovaalkyl chain ; retention times ; molecular mechanics ; Van der Waals interactions
    Vědní obor RIVCC - Organická chemie
    Obor OECDOrganic chemistry
    Institucionální podporaUSMH-B - RVO:67985891
    UT WOS000418212000050
    EID SCOPUS85032383670
    DOI10.1016/j.molstruc.2017.10.068
    AnotaceThe alkyl side chains of n-alkyl phenols, n-alkyl benzenes and n-alkyl naphthalenes are cyclised, as demonstrated by GC measurements, FTIR spectroscopy and molecular mechanics calculations. Cyclisation occurs due to the intramolecular interaction between an aromatic ring (-delta) and a hydrogen of the terminal methyl group (+delta) of an alkyl chain. In fact, conventional molecules are not aliphatic aromatic, but quasi-alicyclic aromatic. With the aromatic molecules formed with a quasi-alicyclic ring, the effect of van der Waals attractive forces increases not only intramolecularly but also intermolecularly. This effect is strong in molecules with propyl and higher alkyl substituents. The increase of intermolecular van der Waals attractive forces results in bi-linearity in the GC retention time of the compounds in question, observed in the dependence of the logarithm of the relative retention time on the number of carbons in a molecule in both polar and nonpolar stationary phases with both capillary and packed columns. The role of van der Waals forces has been demonstrated using the potential energies of covalent and noncovalent interactions for 2-n-alkyl phenols, n-alkyl benzenes and 1-n-alkyl- and 2-n-alkyl naphthalenes.
    PracovištěÚstav struktury a mechaniky hornin
    KontaktIva Švihálková, svihalkova@irsm.cas.cz, Tel.: 266 009 216
    Rok sběru2019
Počet záznamů: 1  

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