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The Cyclization of AlkylSide Chains of Naphthalenes: The GC/Potentila Energies/FTIR Approach

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22320%2F14%3A43897236" target="_blank" >RIV/60461373:22320/14:43897236 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22810/14:43897236

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    The Cyclization of AlkylSide Chains of Naphthalenes: The GC/Potentila Energies/FTIR Approach

  • Original language description

    Gas chromatographic measurements of the retention times of alkyl naphthalenes on packed columns with polar and non-polar stationary phases have proven that the logarithm of the relative retention time increases bi-linearly (not linearly) with the numberof carbon atoms in a molecule. This is caused by a strong inclination of alkyl side chains toward intramolecular cyclization. A FTIR spectral analysis has shown that longer alkyl side chains of alkyl naphthalenes are cyclized through an interaction between the terminal CH3 group and the aromatic ring. Conventional aromatic-aliphatic molecules thus become new molecules with quasi-alicyclic rings. This, however, alters the effect of non-covalent van der Waals attractive forces both inside and outside themolecules, which is reflected in an exponential increase of the retention times of alkyl naphthalenes with a side chain longer than propyl and in the bi-linearity of the logarithmic dependence of the relative retention times on the number

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CI - Industrial chemistry and chemical engineering

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    American Journal of Analytical chemistry

  • ISSN

    2156-8251

  • e-ISSN

  • Volume of the periodical

    2014

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    957-968

  • UT code for WoS article

  • EID of the result in the Scopus database