- Stereoelectrochemistry of Calixarenes
Number of the records: 1  

Stereoelectrochemistry of Calixarenes

  1. 1.
    SYSNO ASEP0475137
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeConference Paper
    TitleStereoelectrochemistry of Calixarenes
    Author(s) Liška, Alan (UFCH-W) RID, ORCID
    Ludvík, Jiří (UFCH-W) RID, ORCID
    Vojtíšek, P. (CZ)
    Source TitleXXXVII. Moderní elektrochemické metody. Sborník přednášek mezinárodní odborné konference. - Ústí nad Labem : Best servis, 2017 / Navrátil Tomáš ; Fojta Miroslav ; Schwarzová Karolína - ISBN 978-80-905221-5-2
    Pagess. 123-127
    Number of pages5 s.
    Publication formPrint - P
    ActionModerní elektrochemické metody /37./
    Event date15.05.2017 - 19.05.2017
    VEvent locationJetřichovice
    CountryCZ - Czech Republic
    Event typeWRD
    Languageeng - English
    CountryCZ - Czech Republic
    KeywordsCalixarenes ; Thiacalixarenes ; Stereoelectrochemistry
    Subject RIVCG - Electrochemistry
    OECD categoryElectrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
    R&D ProjectsGA17-18108S GA ČR - Czech Science Foundation (CSF)
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000432424300027
    AnnotationThe relationship between the stereochemical properties (shape or molecular geometry in
    general sense) and electrochemical ones (typically number of separate redox proceses, their
    nature and potentials) is very fundamental, however, not easily answerable. The nitro
    substituted calix[4]arenes appeared to be suitable series of compounds enabling correlation of
    electrochemical data (redox potential, current, reversibility) with actual shape, conformation
    and dynamic behavior of the molecules dissolved in solution due to their well defined
    geometry and clear polarographic and voltammetric response. Electrochemical methods can
    be therefore used as a straightforward alternative to e.g. temperature dependent NMR
    spectroscopy. The present contribution is focused on thiacalix[4]arenes, their similarities and
    distinctions from their methylene bridged analogues.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2018
Number of the records: 1  

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