首页> 外文期刊>Analytical and bioanalytical chemistry >Application of the novel 5-chloro-2,2,3,3,4,4,5,5-octafluoro-1-pentyl chloroformate derivatizing agent for the direct determination of highly polar water disinfection byproducts
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Application of the novel 5-chloro-2,2,3,3,4,4,5,5-octafluoro-1-pentyl chloroformate derivatizing agent for the direct determination of highly polar water disinfection byproducts

机译:新型5-氯-2,2,3,3,4,4,5,5-八氟-1-戊基氯甲酸酯衍生剂在直接测定高极性水消毒副产物中的应用

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摘要

A novel derivatizing agent, 5-chloro-2,2,3,3,4,4,5,5-octafluoropentyl chloroformate (ClOFPCF), was synthesized and tested as a reagent for direct water derivatization of highly polar and hydrophilic analytes. Its analytical performance satisfactorily compared to a perfluorinated chloroformate previously described, namely 2,2,3,3,4,4,5,5-octafluoropentyl chloroformate (OFPCF). The chemical properties (reactivity, selectivity, derivatization products, and their chromatographic and spectral features) for ClOFPCF were investigated using a set of 39 highly polar standard analytes, including, among others, hydroxylamine, malic and succinic acids, resorcinol, hydroxybenzaldehyde, and dihydroxybenzoic acid. Upon derivatization, the analytes were extracted from the aqueous solvent and analyzed by gas chromatography (GC)-mass spectrometry (MS) in the electron-capture negative ionization (ECNI) mode. Positive chemical ionization (PCI)-MS was used for confirming the molecular ions, which were virtually absent in the ECNI mass spectra. ClOFPCF showed good reaction efficiency, good chromatographic and spectroscopic properties (better than with OFPCF), good linearity in calibration curves, and low detection limits (0.3-1μg/L). A unique feature of the derivatizations with ClOFPCF, and, in general, highly fluorinated chloroformates, is their effectiveness in reacting with carboxylic, hydroxylic, and aminic groups at once, forming multiply-substituted non-polar derivatives that can be easily extracted from the aqueous phase and determined by GC-ECNI-MS. The entire procedure from raw aqueous sample to ready-to-inject hexane solution of the derivatives requires less than 10 min. Another benefit of this procedure is that it produced stable derivatives, with optimal volatility for GC separation, and high electron affinity, which allows their detection as negative ions at trace level. In addition, their mass spectra exhibits chlorine isotopic patterns that clearly indicate how many polar hydrogens of the analyte undergo derivatization. Finally, derivatization with ClOFPCF was used successfully to identify 13 unknown highly polar disinfection byproducts (DBPs) in ozonated fulvic and humic acid aqueous solutions and in real ozonated drinking water.
机译:合成了一种新型的衍生剂,即5-氯-2,2,3,3,4,4,5,5-八氟戊基氯甲酸酯(ClOFPCF),并已作为高极性和亲水性分析物直接水衍生化的试剂进行了测试。与之前描述的全氟化氯甲酸酯,即2,2,3,3,4,4,4,5,5-八氟氯甲酸氯甲酸酯(OFPCF)相比,其分析性能令人满意。使用一组39种高极性标准分析物研究了ClOFPCF的化学性质(反应性,选择性,衍生化产物及其色谱和光谱特征),其中包括羟胺,苹果酸和琥珀酸,间苯二酚,羟基苯甲醛和二羟基苯甲酸等酸。衍生化后,从水性溶剂中提取分析物,并以电子捕获负电离(ECNI)模式通过气相色谱(GC)-质谱(MS)分析。正化学电离(PCI)-MS用于确认分子离子,在ECNI质谱图中几乎不存在。 ClOFPCF表现出良好的反应效率,良好的色谱和光谱特性(优于OFPCF),良好的校准曲线线性和低检出限(0.3-1μg/ L)。用ClOFPCF(通常是高度氟化的氯甲酸酯)衍生化的独特特征是它们可立即与羧基,羟基和胺基反应,形成可轻松从水溶液中提取的多取代非极性衍生物。并通过GC-ECNI-MS确定。从原始含水样品到衍生物的可立即注入己烷溶液的整个过程需要不到10分钟的时间。此方法的另一个好处是,它可以生成稳定的衍生物,具有最佳的气相色谱分离挥发性和较高的电子亲和力,可将其检测为痕量负离子。此外,它们的质谱图还显示出氯同位素模式,该模式清楚地表明了分析物有多少极性氢经历了衍生作用。最后,用ClOFPCF衍生化成功地鉴定了臭氧化的富氟酸和腐殖酸水溶液以及实际的臭氧化饮用水中的13种未知的高极性消毒副产物(DBP)。

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