Pikulski Michael, Aguilar Apolonio, Brodbelt Jennifer S
Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas 78712-0165, USA.
J Am Soc Mass Spectrom. 2007 Mar;18(3):422-31. doi: 10.1016/j.jasms.2006.10.011. Epub 2006 Nov 16.
A tunable ESI-MS/MS strategy for differentiation of flavone and flavanone diglycoside isomers based on metal complexation with auxiliary ligands is reported. The addition of a metal salt and an auxiliary ligand to a flavonoid solution results in the formation of M(II) (flavonoid-H) auxiliary ligand complexes, where M(II) is a transition metal. A series of auxiliary ligands with electron-withdrawing substituents were synthesized to tailor the relative metal binding affinities of the ligands and thus directly influence the stabilities, and consequently the dissociation pathways, of the complexes. Upon collisionally activated dissociation, the complexes yield fragmentation patterns in which the abundances of key diagnostic ions are enhanced, thus facilitating isomer differentiation.
报道了一种基于与辅助配体形成金属配合物来区分黄酮和黄烷酮二糖苷异构体的可调谐电喷雾串联质谱(ESI-MS/MS)策略。向黄酮溶液中加入金属盐和辅助配体可形成M(II)(黄酮-H)辅助配体配合物,其中M(II)为过渡金属。合成了一系列带有吸电子取代基的辅助配体,以调整配体的相对金属结合亲和力,从而直接影响配合物的稳定性,进而影响其解离途径。在碰撞激活解离时,这些配合物产生的碎片模式中关键诊断离子的丰度增加,从而便于异构体的区分。