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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Mechanism of [M + H]~+ Formation in Atmospheric Pressure Photoionization Mass Spectrometry: Identification of Propionitrile in Acetonitrile with High Mass Accuracy Measurement and Tandem Mass Spectrometry and Evidence for Its Involvement in the Prot
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Mechanism of [M + H]~+ Formation in Atmospheric Pressure Photoionization Mass Spectrometry: Identification of Propionitrile in Acetonitrile with High Mass Accuracy Measurement and Tandem Mass Spectrometry and Evidence for Its Involvement in the Prot

机译:大气压光电离质谱法中[M + H]〜+形成的机理:乙炔中丙腈的高精度质谱测定和串联质谱鉴定及其参与质子的证据

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The role of propionitrile in the production of [M + H](+) under atmospheric pressure photoionization (APPI) was investigated. In dopant-assisted APPI using acetone and anisole, protonated acetone and anisole radical cations were the most prominent ions observed. In dopant-free or direct APPI in acetonitrile, however, a major ion in acetonitrile was detected and identified as propionitrile, using high accuracy mass measurement and collision induced c dissociation studies. Vaporizing ca. 10(-5) M althiazide and bendroflumethazide under direct APPI in acetonitrile produced their corresponding protonated species [M + H](+). In addition to protonated acetonitrile, its dimers, and acetonitrile/water clusters, protonated propionitrile, propionitrile dimer, and propionitrile/water clusters were also observed. The role of propionitrile, an impurity in acetonitrile and/or a possible product of ion-molecule reaction, in the production of [M + H](+) of althiazide and bendroflumethazide was further investigated in the absence of dopant using propionitrile-d(5). The formation of [M + D](+) species was observed, suggesting a possible role of propionitrile in the protonation process. Additionally, an increase in the [M + H](+) signal of althiazide and bendroflumethazide was observed as a function of propionitrile concentration in acetonitrile. Theoretical data from the literature supported the assumption that one possible mechanism, among others, for the formation of [M + H](+) could be attributed to photo-initiated isomerization of propionitrile. The most stable isomers of propionitrile, based on their calculated ionization energy (IE) and relative energy (Delta E), were assumed to undergo proton transfer to the analytes, and mechanisms were proposed. (J Am Soc Mass Spectrom 2008, 19, 1579-1589) (C) 2008 American Society for Mass Spectrometry
机译:研究了大气压光电离(APPI)下丙腈在[M + H](+)生产中的作用。在使用丙酮和苯甲醚的掺杂剂辅助的APPI中,质子化的丙酮和苯甲醚自由基阳离子是观察到的最突出的离子。然而,在乙腈中的无掺杂剂或直接的APPI中,使用高精度质量测量和碰撞诱导的c分解研究,可检测到乙腈中的主要离子并将其鉴定为丙腈。蒸发量直接在APPI下在乙腈中的10(-5)甲硫叠氮和苯达氟甲肼产生了相应的质子化物种[M + H](+)。除质子化的乙腈外,还观察到其二聚体和乙腈/水簇,质子化的丙腈,丙腈二聚体和丙腈/水簇。在没有掺杂物的情况下,使用丙腈-d()进一步研究了丙腈(乙腈中的杂质和/或离子分子反应的可能产物)在乙二叠氮和苯并氟甲叠氮[M + H](+)的生产中的作用。 5)。观察到[M + D](+)物种的形成,表明丙腈在质子化过程中可能发挥作用。另外,观察到乙丙酰胺和苯达氟甲肼的[M + H](+)信号增加,这是乙腈中丙腈浓度的函数。来自文献的理论数据支持以下假设:一种可能的机制,其中[M + H](+)的形成可归因于丙腈的光引发异构化。假定丙腈的最稳定异构体基于其计算的电离能(IE)和相对能量(Delta E),经历了质子转移到分析物的过程,并提出了机理。 (J Am Soc Mass Spectrom 2008,19,1579-1589)(C)2008美国质谱学会

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