Experimental and theoretical studies are presented on the reactivity of H2CNH•+ (methanimine) and HCNH2•+ (aminomethylene) with ethene (C2H4). Selective isomer generation is performed via dissociative photoionization of suitable neutral precursors and reactive cross sections and branching ratios are measured as a function of photon and collision energies. Differences between isomers’ reactivity are discussed in light of ab-initio calculations on reaction mechanisms. The main products, for both isomers, are H-elimination, most likely occurring from covalently bound adducts (giving c-CH2CH2CHNH+/CH2NHCHCH2+) and H• atom transfer to yield H2CNH2+. The astrochemical implications of the results are briefly addressed.
The reactivity of methanimine radical cation (H2CNH•+) and its isomer aminomethylene (HCNH2•+) with C2H4 / Sundelin, D.; Ascenzi, D.; Richardson, V.; Alcaraz, C.; Polášek, M.; Romanzin, C.; Thissen, R.; Tosi, P.; Žabka, J.; Geppert, W.. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - 777:(2021), pp. 138677.1-138677.9. [10.1016/j.cplett.2021.138677]
The reactivity of methanimine radical cation (H2CNH•+) and its isomer aminomethylene (HCNH2•+) with C2H4
Ascenzi D.;Richardson V.;Tosi P.;
2021-01-01
Abstract
Experimental and theoretical studies are presented on the reactivity of H2CNH•+ (methanimine) and HCNH2•+ (aminomethylene) with ethene (C2H4). Selective isomer generation is performed via dissociative photoionization of suitable neutral precursors and reactive cross sections and branching ratios are measured as a function of photon and collision energies. Differences between isomers’ reactivity are discussed in light of ab-initio calculations on reaction mechanisms. The main products, for both isomers, are H-elimination, most likely occurring from covalently bound adducts (giving c-CH2CH2CHNH+/CH2NHCHCH2+) and H• atom transfer to yield H2CNH2+. The astrochemical implications of the results are briefly addressed.File | Dimensione | Formato | |
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