Eyres Graham T, Urban Sylvia, Morrison Paul D, Dufour Jean-Pierre, Marriott Philip J
Australian Centre for Research on Separation Science, School of Applied Sciences, RMIT University, G.P.O. Box 2476V, Melbourne, Victoria 3001, Australia.
Anal Chem. 2008 Aug 15;80(16):6293-9. doi: 10.1021/ac8007847. Epub 2008 Jul 23.
Absolute chemical identification requires obtaining a pure compound followed by structure elucidation using spectroscopic techniques, principally NMR spectroscopy and mass spectrometry. Classical isolation techniques suffer from insufficient resolution for complex samples, requiring time-consuming fractionation in multiple steps. Here, a novel preparative technique based upon capillary column multidimensional gas chromatography (MDGC) with 2D NMR to resolve, isolate, and identify pure volatile components from a complex sample is described. As a model application, geraniol was isolated from an essential oil matrix using MDGC and quantitatively resolved from 15 partially coeluting compounds from the first column. Geraniol was recovered from 10 (8.6 microg) and 100 injections (77.6 microg; purity >99%) for subsequent NMR analysis at 500 and 800 MHz (with cryoprobe). Proton and gCOSY NMR experiments were successfully performed at 12.3 microg/mL (10 injections), while gHSQC and gHMBC NMR experiments were obtained at 110.8 microg/mL (100 injections). This approach is applicable to the biodiscovery of volatile molecular species or, indeed, any volatile compound in a complex matrix that requires confirmation of component identity.
绝对化学鉴定需要先获得纯净化合物,然后使用光谱技术(主要是核磁共振光谱和质谱)进行结构解析。传统的分离技术对于复杂样品的分辨率不足,需要进行多步耗时的分馏。本文描述了一种基于毛细管柱多维气相色谱(MDGC)与二维核磁共振(2D NMR)的新型制备技术,用于从复杂样品中分离、鉴定和解析纯挥发性成分。作为一个模型应用,使用MDGC从香精油基质中分离出香叶醇,并从第一根色谱柱上与15种部分共洗脱的化合物中进行定量解析。从10次进样(8.6微克)和100次进样(77.6微克;纯度>99%)中回收香叶醇,用于后续在500和800兆赫(配备低温探头)下的核磁共振分析。在12.3微克/毫升(10次进样)时成功进行了质子和gCOSY核磁共振实验,而在110.8微克/毫升(100次进样)时获得了gHSQC和gHMBC核磁共振实验结果。这种方法适用于挥发性分子物种的生物发现,或者实际上适用于任何需要确认成分身份的复杂基质中的挥发性化合物。