Formation of [Cu(CO2)(CH3OH)]+ and [Cu(N2)(CH3OH)]+ by gas-phase dissociation and exchange reactions

被引:0
|
作者
Metzler, Luke J. [1 ]
Koehler, Stephen [1 ]
Somogyi, Arpad [2 ]
Van Stipdonk, Michael J. [1 ]
机构
[1] Duquesne Univ, Dept Chem & Biochem, Pittsburgh, PA 15219 USA
[2] Ohio State Univ, Campus Chem Instrument Ctr, Mass Spectrometry & Prote Facil, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
Electrospray ionization; Ion trap mass spectrometry; Metal ion complexes; Ion-molecule reactions; Copper ion; Carbon dioxide; CHEMISTRY; REACTIVITY; CL;
D O I
10.1016/j.ijms.2018.10.030
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Electrospray ionization and multiple-stage tandem mass spectrometry were used to study the collision-induced dissociation of methanol-coordinated copper-acetate cations, and the ion-molecule reactions of specific product ions. Our experiments led to the discovery of unusual gas-phase ions with compositions such as [Cu(CO2)(CH3OH)](+) and [Cu(N-2)(CH3OH)](+). The latter is generated by spontaneous exchange of CO2 for N-2 in an ion-molecule reaction. Isotopic labeling studies and high mass-resolution measurements provide data to support the product ion composition assignments. Density functional theory calculations corroborate the experimental observations, both with respect to the preferential decarboxylation over methanol ligand elimination, and the spontaneous nature of the ion-molecule reactions. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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