Anion formation in gas-phase potassium-uridine collisions

被引:9
|
作者
Almeida, D. [1 ]
da Silva, F. Ferreira [1 ]
Kopyra, J. [2 ]
Garcia, G. [3 ,4 ]
Limao-Vieira, P. [1 ,5 ]
机构
[1] Univ Nova Lisboa, Dept Fis, Fac Ciencias & Tecnol, Lab Colisoes Atom & Mol,CEFITEC, P-2829516 Caparica, Portugal
[2] Siedlce Univ, Dept Chem, PL-08110 Siedlce, Poland
[3] CSIC, Inst Fis Fundamental, E-28006 Madrid, Spain
[4] Univ Wollongong, Ctr Med Radiat Phys, Wollongong, NSW 2522, Australia
[5] Open Univ, Dept Phys Sci, Milton Keynes MK7 6AA, Bucks, England
关键词
Nucleoside; Uridine; Negative ion; Atomic collisions; Electron transfer; DISSOCIATIVE ELECTRON-ATTACHMENT; LOW-ENERGY ELECTRONS; PYRIMIDINE-BASES; FRAGMENTATION; THYMIDINE; URACIL;
D O I
10.1016/j.ijms.2014.01.023
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
In this study we report negative ion fragmentation patterns obtained from time-of-flight (TOF) mass spectrometry in potassium-uridine collisions at 30, 70 and 100 eV. The dominant fragments from uridine are also the most abundant from the individual units in potassium collisions with uracil, tetrahydrofuran (THF) and D-ribose. We observe no dehydrogenated parent anion formation. Special emphasis is given to the dissociation mechanisms lending support to the breaking of the N-glycosidic bond as an initial step in the fragmentation of the transient negative ion (TNI). Within their role as sugar unit surrogates, THF and D-ribose (DR) provide useful information for the study of uridine, and presumably other nucleosides from the point of view of DNA/RNA subunits integrity in the biological environment. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:243 / 247
页数:5
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