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在电喷雾电离质谱条件下,单氧钼(VI)配合物中氧原子转移反应的分叉途径。

A bifurcated pathway of oxygen atom transfer reactions from a monooxo molybdenum(VI) complex under electrospray ionisation mass spectrometric conditions.

作者信息

Nemykin Victor N, Basu Partha

机构信息

Department of Chemistry and Biochemistry, Duquesne University, Pittsburgh, 15282 PA, USA.

出版信息

Dalton Trans. 2004 Jul 7(13):1928-33. doi: 10.1039/b403964e. Epub 2004 Jun 1.

Abstract

A stable molybdenum(V) complex, LMoOCl2(where L is hydrotris(3,5-dimethylpyrazolyl)borate), has been oxidized under mass spectrometric conditions. The oxidized species reacts with tertiary phosphines and the products have been detected by mass spectrometry. The product distribution has been followed by isotope labeling experiments, and energy dependent electrospray mass spectrometry. These experiments reveal not only oxygen atom transfer but also loss of a chlorine atom from the resulting species.

摘要

一种稳定的钼(V)配合物LMoOCl₂(其中L为氢化三(3,5 - 二甲基吡唑基)硼酸酯)在质谱条件下被氧化。氧化产物与叔膦反应,产物通过质谱检测。通过同位素标记实验和能量依赖型电喷雾质谱跟踪产物分布。这些实验不仅揭示了氧原子转移,还揭示了所得物种中氯原子的损失。

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