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Solid State Nuclear Magnetic Resonance as a Tool to Explore Solvent-Free MALDI Samples

机译:固态核磁共振作为探索无溶剂MALDI样品的工具

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Solid-state Nuclear magnetic resonance (NMR) was used here to explore structural characteristics of samples to be subjected to matrix-assisted laser desorption/ionization (MALDI) and prepared without the use of any solvent. The analytical systems scrutinized in NMR were mixtures of a 2,5-dihydroxybenzoic acid (2,5-DHB) matrix and caesium fluoride (CsF), used as the cationization agent in synthetic polymer MALDI mass analysis, at different molar ratios (1:1, 5:1, and 10:1). Complementary information could be obtained from C-13, Cs-133, and F-19 NMR spectra. Grinding the matrix together with the salt in the solid state was shown to induce a strong modification in the molecular organization within the MALDI sample. The evidenced mechano-induced reactions allow strong interactions between the matrix and the cation, up to the formation of a salt, and only occur in the presence of some water molecules. Addition of a poly(ethylene oxide) polymer as the analyte did not further modify the observed molecular organizations. Although relative matrix and salt concentrations in the scrutinized samples were unusual for MALDI analysis, mass spectra of good quality could be obtained and revealed that cation attachment on polymers during the MALDI. process is not a matrix-independent event since a lower ionization efficiency was obtained from highly organized solid samples, mostly consisting of 2,5-DHB caesium salt species. (J Am Soc Mass Spectrom 2009, 20, 1906-1911)
机译:此处使用固态核磁共振(NMR)来研究样品的结构特征,该样品将进行基质辅助激光解吸/电离(MALDI),并且无需使用任何溶剂即可制备。在NMR中仔细检查的分析系统是2,5-二羟基苯甲酸(2,5-DHB)基质和氟化铯(CsF)的混合物,用作合成聚合物MALDI质量分析中的阳离子化剂,摩尔比不同(1: 1、5:1和10:1)。补充信息可以从C-13,Cs-133和F-19 NMR光谱获得。显示将基质与固态盐一起研磨会引起MALDI样品内分子组织的强烈修饰。证据表明,机械诱导的反应允许基质与阳离子之间发生强烈的相互作用,直至形成盐为止,并且仅在某些水分子存在下才会发生。添加聚(环氧乙烷)聚合物作为分析物并没有进一步改变观察到的分子组织。尽管对于MALDI分析来说,被检查样品中的相对基质和盐浓度是不寻常的,但是可以获得高质量的质谱,并且揭示了MALDI期间阳离子附着在聚合物上。该过程不是与基质无关的事件,因为从高度组织化的固体样品(主要由2,5-DHB铯盐类物质组成)中获得较低的电离效率。 (J Am Soc质谱2009,20,1906-1911)

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