Charge Reversal Fourier Transform Ion Cyclotron Resonance Mass Spectrometry

被引:1
作者
Lobodin, Vladislav V. [1 ]
Savory, Joshua J. [1 ]
Kaiser, Nathan K. [1 ]
Dunk, Paul W. [2 ]
Marshall, Alan G. [1 ,2 ]
机构
[1] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[2] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
关键词
Charge inversion; Ion activation; Fourier transform; FTMS; FT-ICR; ICR; Penning trap; Double electron transfer; Single electron transfer; Neutralization-reionization; COLLISION-INDUCED DISSOCIATION; ELECTRON-IMPACT EXCITATION; NEGATIVE-IONS; GAS-PHASE; PERMUTATION REACTIONS; AXIALIZATION; INVERSION; SPECTRA; DENSITY; CELL;
D O I
10.1007/s13361-012-0512-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report the first charge reversal experiments performed by tandem-in-time rather than tandem-in-space MS/MS. Precursor odd-electron anions from fullerene C-60, and even-electron ions from 2,7-di-tert-butylfluorene-9-carboxylic acid and 3,3'-bicarbazole were converted into positive product ions (-CR+) inside the magnet of a Fourier transform ion cyclotron resonance mass spectrometer. Charge reversal was activated by irradiating precursor ions with high energy electrons or UV photons: the first reported use of those activation methods for charge reversal. We suggest that high energy electrons achieve charge reversal in one step as double electron transfer, whereas UV-activated -CR+ takes place stepwise through two single electron transfers and formally corresponds to a neutralization-reionization (-NR+) experiment.
引用
收藏
页码:213 / 221
页数:9
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