Fabre N, Rustan I, de Hoffmann E, Quetin-Leclercq J
Laboratoire de Pharmacognosie, Université Catholique de Louvain, Brussels, Belgium.
J Am Soc Mass Spectrom. 2001 Jun;12(6):707-15. doi: 10.1016/S1044-0305(01)00226-4.
Eleven naturally occurring flavonoid aglycones, belonging to the representative flavone, flavonol, and flavanone types were separated by high performance liquid chromatography and analyzed on-line with negative ion electrospray ionization tandem mass spectrometry (ESI-MS/MS). In order to resolve the MS/MS spectra obtained, each compound was reinvestigated by direct loop injections using an ion trap mass spectrometer. The MSn spectra obtained allowed us to propose plausible schemes for their fragmentation supported by the analysis of five complementary synthetic flavonoid aglycones. The negative ion ESI-MS/MS behavior of the different aglycones investigated in this study revealed interesting differences when compared with the previously described patterns obtained using various ionization techniques in positive ion. Thus, concerning the retro Diels-Alder (RDA) fragmentation pathways, several structurally informative anions appeared highly specific of the negative ion mode. In addition, a new lactone-type structure, instead of a ketene, was proposed for a classic RDA diagnostic ion. We also observed unusual CO, CO2, and C3O2 losses which appear to be characteristic of the negative ion mode. All these results and these unusual neutral losses show that the negative ion mode was a powerful complementary tool of the positive ion mode for the structural characterization of flavonoid aglycones by ESI-MS/MS.
通过高效液相色谱法分离出11种天然存在的黄酮苷元,它们分别属于代表性的黄酮、黄酮醇和黄烷酮类型,并采用负离子电喷雾电离串联质谱法(ESI-MS/MS)进行在线分析。为了解析所获得的MS/MS谱图,使用离子阱质谱仪通过直接环进样对每种化合物进行了重新研究。所获得的MSn谱图使我们能够在对5种互补的合成黄酮苷元进行分析的支持下,提出它们的碎片化合理方案。与之前使用各种电离技术在正离子模式下获得的模式相比,本研究中所研究的不同苷元的负离子ESI-MS/MS行为显示出有趣的差异。因此,关于逆狄尔斯-阿尔德(RDA)碎片化途径,几种具有结构信息的阴离子在负离子模式下显得具有高度特异性。此外,针对一种经典的RDA诊断离子,提出了一种新的内酯型结构,而非烯酮结构。我们还观察到了不寻常的CO、CO2和C3O2损失,这些损失似乎是负离子模式的特征。所有这些结果以及这些不寻常的中性损失表明,负离子模式是正离子模式通过ESI-MS/MS对黄酮苷元进行结构表征的有力补充工具。