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An experimental study of the reactivity of CN and C3N anions with cyanoacetylene (HC3N)
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SYSNO ASEP 0467289 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title An 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 Title Icarus. - : Elsevier - ISSN 0019-1035
Roč. 268, APR 2016 (2016), s. 242-252Number of pages 11 s. Language eng - English Country US - United States Keywords ionosoheres ; titan ; satellites Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects GA14-19693S GA ČR - Czech Science Foundation (CSF) LD14024 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support UFCH-W - RVO:61388955 UT WOS 000370218100017 EID SCOPUS 84955636488 DOI https://doi.org/10.1016/j.icarus.2015.12.001 Annotation The 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. Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2017
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