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顺铂类似物的快原子轰击质谱分析

Fast atom bombardment mass spectrometry of cisplatin analogs.

作者信息

Siegel M M, Bitha P, Child R G, Hlavka J J, Lin Y I, Chang T T

出版信息

Biomed Environ Mass Spectrom. 1986 Jan;13(1):25-32. doi: 10.1002/bms.1200130106.

Abstract

Cisplatin analogs of the type PtLACl2 and PtLALB are thermally unstable, non-volatile and highly insoluble. For these platinum coordination complexes, LA is a bidentate amine ligand and LB is a bidentate carboxylate ligand. Mass spectral data for structural elucidation of these compounds are absent in the literature because they are difficult to ionize. Nevertheless, a routine fast atom bombardment mass spectroscopic method has been developed utilizing the mixed solvent system of dimethyl sulfoxide:thioglycerol in a ratio of about 1:3 v/v. Using both positive and negative ionization modes, structurally significant ions were observed from representative molecules of the two named classes of compounds. [M-H]- ions were observed in both structural classes while [M + H]+ ions were observed only in the PtLALB class of compounds. Additional ions observed are rationalized in terms of the condensed-phase solution chemistry of the cisplatin analogs and the mixed solvent system when exposed to the fast atom beam. The two mechanisms causing ionization of the cisplatin analogs in the condensed phase appear to be: displacement of the ligands with dimethyl-sulfoxide and addition of chloride and the ionized solvents [dimentyl sulfoxide + H]+ and [thioglycerol - H]- to the cisplatin analogs. It is hypothesized that the addition reactions of the ionized solvents occur because of the differences in the basicity of the solvents and their reactivity in forming platinum(II)-sulfur bonds.

摘要

PtLACl2和PtLALB类型的顺铂类似物热不稳定、不挥发且极难溶解。对于这些铂配位络合物,LA是双齿胺配体,LB是双齿羧酸盐配体。由于这些化合物难以电离,文献中缺乏用于其结构解析的质谱数据。然而,已开发出一种常规的快速原子轰击质谱方法,该方法使用二甲基亚砜与硫代甘油比例约为1:3 v/v的混合溶剂体系。利用正离子和负离子电离模式,从这两类指定化合物的代表性分子中观察到了具有结构意义的离子。在这两类结构中均观察到了[M-H]-离子,而仅在PtLALB类化合物中观察到了[M + H]+离子。根据顺铂类似物的凝聚相溶液化学以及暴露于快速原子束时的混合溶剂体系,对观察到的其他离子进行了合理解释。顺铂类似物在凝聚相中发生电离的两种机制似乎是:配体被二甲基亚砜取代,以及氯和离子化溶剂[二甲基亚砜 + H]+和[硫代甘油 - H]-加成到顺铂类似物上。据推测,离子化溶剂的加成反应是由于溶剂碱性的差异及其在形成铂(II)-硫键时的反应性不同所致。

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