首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Differentiation of isomeric cresols by silylation in combination with gas chromatography/mass spectrometry analysis
【24h】

Differentiation of isomeric cresols by silylation in combination with gas chromatography/mass spectrometry analysis

机译:用气相色谱/质谱分析将异构甲酚的分化与气相色谱/质谱分析相结合

获取原文
获取原文并翻译 | 示例
           

摘要

Rationale m-Cresol is listed as a priority controlled contaminant in many countries, but it is very difficult to accurately determine isomeric cresols due to their incomplete chromatographic separation on commercially available chromatographic columns and their nearly identical mass spectra. Methods Silylation of isomeric cresols was carried out by treatment with N-methyl-N-(trimethylsilyl)trifluoroacetamide. The formed trimethyl(tolyloxy)silanes were analyzed by gas chromatography/mass spectrometry (GC/MS). Theoretical calculations were carried out with the Gaussian 03 program using the density functional theory (DFT) method at the B3LYP/6-311 + G(2d,p) level. Results The derivatives of three isomeric cresols and six isomeric xylenols have been completely separated on an HP-5MS capillary column within a GC run of only 10 minutes. In addition, the derivative o-cresol can be very easily differentiated from its isomers due to its characteristic base peak ion at m/z 91 in electron ionization (EI)-MS. DFT calculation results indicated that the formation of the abundant fragment ion at m/z 91 is attributed to a facile dissociation pathway involving the shift of a neighboring phenylmethyl hydrogen atom in EI-MS of trimethyl(o-tolyloxy)silane. Conclusions Silylation provides a promising solution for simultaneous determination of isomeric cresols and isomeric xylenols.
机译:理由M-CRESOL被列为许多国家的优先权受控污染物,但由于它们在市售的色谱柱上的不完全色谱分离及其几乎相同的质谱,因此非常困难地确定异构克罗索尔。方法通过用N-甲基-N-(三甲基甲硅烷基)三氟乙酰胺处理进行异构甲酚的甲硅烷基化。通过气相色谱/质谱(GC / MS)分析形成的三甲基(甲苯氧基)硅烷。在B3LYP / 6-311 + G(2D,P)水平下使用密度泛函理论(DFT)方法进行高斯03程序进行理论计算。结果三种异构甲酚和六个异构甲酚的衍生物在仅10分钟的GC运行的HP-5MS毛细管柱上完全分离。此外,由于其在电子电离(EI)-MS中的M / Z 91的特征基峰离子,衍生物O-甲酚可以非常容易地从其异构体分化。 DFT计算结果表明,M / Z 91的丰富片段离子的形成归因于容易解离途径,涉及在三甲基(甲苯氧基)硅烷的EI-MS中的相邻苯甲基氢原子的偏移。结论甲硅烷基化提供了一种有前途的解决方案,用于同时测定异构甲酚和异构甲烯醇。

著录项

  • 来源
  • 作者单位

    Hangzhou Normal Univ Key Lab Organosilicon Chem &

    Mat Technol Hangzhou 311121 Peoples R China;

    Zhejiang Prov Environm Monitoring Ctr Hangzhou 310015 Peoples R China;

    Hangzhou Normal Univ Key Lab Organosilicon Chem &

    Mat Technol Hangzhou 311121 Peoples R China;

    Zhejiang Prov Environm Monitoring Ctr Hangzhou 310015 Peoples R China;

    Hangzhou Normal Univ Key Lab Organosilicon Chem &

    Mat Technol Hangzhou 311121 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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