Gross Jürgen H
Institute of Organic Chemistry, University of Heidelberg, Heidelberg, Germany.
J Am Soc Mass Spectrom. 2007 Dec;18(12):2254-62. doi: 10.1016/j.jasms.2007.09.019. Epub 2007 Oct 2.
Ten ionic liquids based on four types of organic cations, C(+) (imidazolium, pyrrolidinium, pyridinium, and phosphonium), combined with various types of anions, A-, were analyzed by liquid injection field desorption/ionization- (LIFDI) mass spectrometry. For the purpose of LIFDI analysis the ionic liquids were dissolved in methanol, acetonitrile or tetrahydrofuran at concentrations of 0.01-0.1 microl mL(-1). The measurements were performed on a double-focusing magnetic sector instrument. In all ionic liquid LIFDI spectra, the intact cation of the compound yielded the base peak accompanied by cluster ions of the general formula C(2)A and occasionally C(3)A(2). Tandem mass spectrometry and reconstructed ion chromatograms were employed to reveal the identity of the observed ions. Although limited to positive-ion mode, LIFDI also provided analytical information on the anions due to cluster ion formation. Depending on actual emitter condition and ionic liquid the limit of detection in survey scans was determined to 5-50 pg of ionic liquid.
通过液体进样场解吸/电离-(LIFDI)质谱分析了基于四种有机阳离子(C⁺,即咪唑鎓、吡咯烷鎓、吡啶鎓和鏻)与各种类型阴离子(A⁻)组合而成的十种离子液体。为了进行LIFDI分析,将离子液体以0.01 - 0.1微升/毫升的浓度溶解在甲醇、乙腈或四氢呋喃中。测量在双聚焦磁扇形仪器上进行。在所有离子液体的LIFDI光谱中,化合物的完整阳离子产生基峰,并伴有通式为[C₂A]⁺的簇离子,偶尔还有[C₃A₂]⁺。采用串联质谱和重建离子色谱图来揭示所观察到的离子的身份。尽管限于正离子模式,但由于簇离子的形成,LIFDI也提供了有关阴离子的分析信息。根据实际的发射器条件和离子液体,在全扫描中的检测限确定为5 - 50皮克离子液体。