Anionic Reactions Degrading SF6 Using Metals: Insights From the Gas Phase

IF 1.8 3区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Rapid Communications in Mass Spectrometry Pub Date : 2024-11-26 DOI:10.1002/rcm.9948
Shiven Joshi, Sharon Barden, Paul M. Mayer
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Abstract

Alkali metals have been used to degrade SF6 in liquid ammonia. The products include metal fluorides. In this study, we reacted K and Ag with SF6 in a triple quadrupole mass spectrometer. The atomic metal anions were formed by in-source collision-induced dissociation (CID) of their respective oxalate salts as previously described by our group. The only two reaction products observed were SF6 and SF5. At low collision energy, the latter was deduced to be formed via an abstraction by the metal of F from SF6 formed by electron transfer in the encounter complex between the metal anion and neutral SF6. As the collision energy was increased, there was evidence of a CID contribution to SF5 directly from SF6.

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利用金属降解 SF6 的阴离子反应:气相的启示。
碱金属已被用于降解液氨中的 SF6。其产物包括金属氟化物。在这项研究中,我们在三重四极杆质谱仪中将 K- 和 Ag- 与 SF6 反应。原子金属阴离子是通过各自的草酸盐盐的源内碰撞诱导解离(CID)形成的,正如我们小组之前所描述的那样。观察到的唯一两种反应产物是 SF6 - 和 SF5 -。在低碰撞能下,后者被推断为是通过金属从 SF6 - 中抽取 F 形成的,而 SF6 - 是在金属阴离子和中性 SF6 - 的相遇复合物中通过电子转移形成的。随着碰撞能量的增加,有证据表明,SF5 - 直接来自 SF6 - 的 CID 贡献。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
219
审稿时长
2.6 months
期刊介绍: Rapid Communications in Mass Spectrometry is a journal whose aim is the rapid publication of original research results and ideas on all aspects of the science of gas-phase ions; it covers all the associated scientific disciplines. There is no formal limit on paper length ("rapid" is not synonymous with "brief"), but papers should be of a length that is commensurate with the importance and complexity of the results being reported. Contributions may be theoretical or practical in nature; they may deal with methods, techniques and applications, or with the interpretation of results; they may cover any area in science that depends directly on measurements made upon gaseous ions or that is associated with such measurements.
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