首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Mass spectral characterization of the CWC-related isomeric dialkyl alkylphosphonothiolates/alkylphosphonothionates under gas chromatography/mass spectrometry conditions
【24h】

Mass spectral characterization of the CWC-related isomeric dialkyl alkylphosphonothiolates/alkylphosphonothionates under gas chromatography/mass spectrometry conditions

机译:气相色谱/质谱分析条件下CWC相关异构的二烷基烷基硫代磷酸二烷基酯/硫代磷酸烷基酯的质谱表征

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

RATIONALE The isomeric dialkyl alkylphosphonothiolates and dialkyl alkylphosphonothionates are listed as scheduled chemicals of the Chemical Weapons Convention (CWC) implemented by the OPCW. The P-S and P-R bond connectivity has to be correctly identified for the verification of the CWC. The present study demonstrates successful identification of the target isomers by selective fragmentation under electron ionization (EI) or chemical ionization (CI) conditions. METHODS All the studied isomeric compounds (27 in total) were synthesized in our laboratory using established methods, then analyzed by EI and CI gas chromatography/mass spectrometry (GC/MS) using an Agilent 6890 gas chromatograph equipped with a HP-5MS capillary column and interfaced to a 5973 N mass-selective detector. The retention index (RI) values of all the compounds were calculated using Van den Dool's formula. GC/MS/MS and GC/HRMS experiments were also performed using a VG-Autospec (magnetic sector) and JEOL-AccuToF (time-of-flight) mass spectrometer, respectively. RESULTS The EI mass spectra of all the compounds had an abundant molecular ion at m/z 182, except in the case of a few selected butyl-substituted compounds, where this ion was of low abundance. The EI fragmentation pathways include α-cleavage, McLafferty rearrangement, McLafferty + 1 rearrangement, O/S-alkyl radical loss, and an alkene loss with a hydrogen shift. The characteristic fragment ions and their relative abundances are significant in elucidating the alkyl group attached to the P/S/O-atoms as well as the P-S/P = S bond connectivity. The EI and CI mass spectra together with RI values enable unambiguous identification of all the studied isomeric compounds. CONCLUSIONS The present study highlights the structural characterization of the isomeric phosphonothiolates and phosphonothionates based on their selective EI fragmentation. The assigned fragmentation pathway helps in the assignment of P-S and P-alkyl connectivity in phosphonothiolates and phosphonothionates, consequently the structure of the unknown compounds. The EI mass spectra (27 compounds) of isomeric compounds are immensely useful in the OPCW official proficiency tests and for off-site analysis.
机译:理由禁化武组织实施的《化学武器公约》(CWC)的列入清单的化学品列为二烷基烷基硫代磷酸二烷基酯和烷基烷基膦酸二烷基酯。必须正确标识P-S和P-R键连接,以验证CWC。本研究证明了在电子电离(EI)或化学电离(CI)条件下通过选择性裂解成功鉴定目标异构体。方法在我们的实验室中,使用既定方法合成了所有研究的异构化合物(共27种),然后使用配备HP-5MS毛细管柱的Agilent 6890气相色谱仪通过EI和CI气相色谱/质谱(GC / MS)进行分析并连接到5973 N质量选择检测器。使用范登杜尔公式计算所有化合物的保留指数(RI)值。还分别使用VG-Autospec(磁性扇区)和JEOL-AccuToF(飞行时间)质谱仪进行了GC / MS / MS和GC / HRMS实验。结果所有化合物的EI质谱在m / z 182处均具有丰富的分子离子,除了少数几种丁基取代的化合物(该离子的丰度较低)外。 EI断裂途径包括α裂解,McLafferty重排,McLafferty +1重排,O / S烷基自由基损失和带有氢位移的烯烃损失。特征性碎片离子及其相对丰度在阐明连接到P / S / O原子的烷基以及P-S / P = S键的连接性方面很重要。 EI和CI质谱以及RI值可以明确鉴定所有研究的异构体化合物。结论本研究着重介绍了基于选择性EI片段化的异硫代磷酸硫代酸酯和硫代磷酸硫代酸酯的结构特征。分配的断裂途径有助于分配膦酰基硫代酸酯和膦酰基硫代酸酯中的P-S和P-烷基连接性,因此有助于未知化合物的结构。异构化合物的EI质谱(27种化合物)在禁化武组织官方能力验证和场外分析中非常有用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号