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The Influences of A Nitrogen Atom Position in Dinucleoside 2-,3-,4-Pyridylphosphonates on Fragmentation Patterns in Electrospray Ionization Multistage Tandem Mass Spectra
Authors:Sanhao Ji  Yong Ju  Hua Fu  Yufen Zhao  Tommy Johansson  Jacek Stawinski
Institution:1. Key Laboratory of Bioorganic Phosphorus Chemistry &2. Chemical Biology, Department of Chemistry , Tsinghua University , Beijing, China;3. Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , Stockholm, Sweden
Abstract:2-,3-,4-Pyridylphosphonates and their phosphonothioate congeners were analyzed by electrospray ionization multistage tandem mass spectrometry (ESI-MSn). It was found that the fragmentation pathways of these compounds were not influenced to any detectable extent by the stereochemistry at the phosphorus centers but were sensitive to the position of a nitrogen atom in the pyridine ring of these compounds. Possible mechanisms for fragmentations of the investigated compounds are discussed in detail.

Keywords:Pyridylphosphonates  Pyridylphosphonothioates  Nitrogen atom  Pyridyl ring  Electrospray ionization spectrometry (ESI)
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