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Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures

The reactivity of closed-shell gas phase cluster anions AuTi(3)O(7)(–) and AuTi(3)O(8)(–) with methane under thermal collision conditions was studied by mass spectrometric experiments and quantum chemical calculations. Methane activation was observed with the formation of AuCH(3) in both cases, whil...

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Autores principales: Zhao, Yan-Xia, Li, Xiao-Na, Yuan, Zhen, Liu, Qing-Yu, Shi, Qiang, He, Sheng-Gui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016522/
https://www.ncbi.nlm.nih.gov/pubmed/30155123
http://dx.doi.org/10.1039/c6sc00539j
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author Zhao, Yan-Xia
Li, Xiao-Na
Yuan, Zhen
Liu, Qing-Yu
Shi, Qiang
He, Sheng-Gui
author_facet Zhao, Yan-Xia
Li, Xiao-Na
Yuan, Zhen
Liu, Qing-Yu
Shi, Qiang
He, Sheng-Gui
author_sort Zhao, Yan-Xia
collection PubMed
description The reactivity of closed-shell gas phase cluster anions AuTi(3)O(7)(–) and AuTi(3)O(8)(–) with methane under thermal collision conditions was studied by mass spectrometric experiments and quantum chemical calculations. Methane activation was observed with the formation of AuCH(3) in both cases, while the formation of formaldehyde was also identified in the reaction system of AuTi(3)O(8)(–). The cooperative effect of the separated Au(+) and O(2–) ions on the clusters induces the cleavage of the first C–H bond of methane. Further activation of the second C–H bond by a peroxide ion O(2)(2–) leads to the formation of formaldehyde. This study shows that closed-shell species on metal oxides can be reactive enough to facilitate thermal H–CH(3) bond cleavage and the subsequent conversion.
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spelling pubmed-60165222018-08-28 Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures Zhao, Yan-Xia Li, Xiao-Na Yuan, Zhen Liu, Qing-Yu Shi, Qiang He, Sheng-Gui Chem Sci Chemistry The reactivity of closed-shell gas phase cluster anions AuTi(3)O(7)(–) and AuTi(3)O(8)(–) with methane under thermal collision conditions was studied by mass spectrometric experiments and quantum chemical calculations. Methane activation was observed with the formation of AuCH(3) in both cases, while the formation of formaldehyde was also identified in the reaction system of AuTi(3)O(8)(–). The cooperative effect of the separated Au(+) and O(2–) ions on the clusters induces the cleavage of the first C–H bond of methane. Further activation of the second C–H bond by a peroxide ion O(2)(2–) leads to the formation of formaldehyde. This study shows that closed-shell species on metal oxides can be reactive enough to facilitate thermal H–CH(3) bond cleavage and the subsequent conversion. Royal Society of Chemistry 2016-07-01 2016-03-29 /pmc/articles/PMC6016522/ /pubmed/30155123 http://dx.doi.org/10.1039/c6sc00539j Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Zhao, Yan-Xia
Li, Xiao-Na
Yuan, Zhen
Liu, Qing-Yu
Shi, Qiang
He, Sheng-Gui
Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title_full Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title_fullStr Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title_full_unstemmed Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title_short Methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
title_sort methane activation by gold-doped titanium oxide cluster anions with closed-shell electronic structures
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016522/
https://www.ncbi.nlm.nih.gov/pubmed/30155123
http://dx.doi.org/10.1039/c6sc00539j
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