Kellner Ina D, Drewello Thomas
Physical Chemistry I, Department of Chemistry and Pharmacy, University of Erlangen-Nürnberg, 91058, Erlangen, Germany.
J Am Soc Mass Spectrom. 2015 Aug;26(8):1328-37. doi: 10.1007/s13361-015-1137-7. Epub 2015 Apr 21.
Singly and doubly charged adducts of LiCl with β-cyclodextrin (βCD) of the type (βCD)(LiCl)(n)Li(+) and (βCD)2(LiCl)(p)Li2(2+) were studied using electrospray ionization mass spectrometry (ESI-MS). Insight into their structural composition was gained by analysis of their collision-induced dissociation (CID) mass spectra. The conditions the ions experience in the transfer region interfacing the ESI source and the mass analyzer were found to have a marked influence on the nature of the detected ions. In one instrument incorporating a single skimmer, individually attached LiCl ion pairs were observed, whereas the dual funnel ion guides of the second instrument allow the detection of previously unknown labile inclusion complexes of (LiCl)n clusters in βCD.
利用电喷雾电离质谱法(ESI-MS)研究了LiCl与β-环糊精(βCD)形成的单电荷和双电荷加合物,其类型为(βCD)(LiCl)(n)Li⁺和(βCD)₂(LiCl)(p)Li₂²⁺。通过分析它们的碰撞诱导解离(CID)质谱,深入了解了它们的结构组成。发现离子在连接ESI源和质量分析仪的传输区域所经历的条件对检测到的离子性质有显著影响。在一台装有单个分离器的仪器中,观察到了单独附着的LiCl离子对,而第二台仪器的双漏斗离子导向器则能够检测到βCD中(LiCl)n簇以前未知的不稳定包合物。