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An experimental study of the reactivity of CN and C3N anions with cyanoacetylene (HC3N)

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    SYSNO ASEP0467289
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAn experimental study of the reactivity of CN and C3N anions with cyanoacetylene (HC3N)
    Author(s) Romanzin, C. (FR)
    Louarn, E. (FR)
    Lemaire, J. (FR)
    Žabka, Ján (UFCH-W) RID, ORCID, SAI
    Polášek, Miroslav (UFCH-W) RID, ORCID
    Guillemin, J.-C. (FR)
    Alcaraz, Ch. (FR)
    Source TitleIcarus. - : Elsevier - ISSN 0019-1035
    Roč. 268, APR 2016 (2016), s. 242-252
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    Keywordsionosoheres ; titan ; satellites
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA14-19693S GA ČR - Czech Science Foundation (CSF)
    LD14024 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000370218100017
    EID SCOPUS84955636488
    DOI https://doi.org/10.1016/j.icarus.2015.12.001
    AnnotationThe reactions of the CN- and C3N- anions with cyanoacetylene HC3N, of special interest for the chemistry of Titan's upper atmosphere, have been investigated by means of FTICR mass-spectrometry. Primary ions, CN- and C3N-, have been produced by dissociative electron attachment (DEA) from BrCN and BrC3N, and prepared in a clean way before reaction. Total rate constants have been measured for both reactions at 300 K and are found to be as follows: (3.9 +/- 0.5) x 10(-9) and (1.0 +/- 0.2) x 10(-10) cm(3) s(-1) for the reaction of HC3N with CN- and C3N-, respectively. For the CN- + HC3N reaction, proton transfer is found to be the only reactive channel within our detection limits. Proton transfer is also dominant for the C3N- + HC3N reaction but the resulting ionic product being identical to the primary ion C3N-, this process is transparent for the kinetics of the C3N- + HC3N reaction and the kinetic rate retrieved corresponds to a slow and competitive detachment pathway. Yet the nature and energetics of the neutral product(s) formed through this process remain unknown. Additional experiments using isotopic products have allowed to retrieve specific rate constants associated with the proton transfer channel in the (C3N-)-N-15 + HC3N and C3N- + (HC3N)-N-15 reactions and the measured rates are found to be significantly lower than for the CN- + HC3N system. This decrease and the evolution of reactivity when going from CN- to C3N- and the opening of a new detachment pathway are finally discussed. (C) 2015 Elsevier Inc. All rights reserved.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2017
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