Literature DB >> 20049883

Investigation of collision-induced dissociations involving odd-electron ion formation under positive electrospray ionization conditions using accurate mass.

Guifen Xu1, Tom Huang, Jennifer Zhang, Jennifer K Huang, Timothy Carlson, Shichang Miao.   

Abstract

Collision induced dissociation (CID) has been extensively used for structure elucidation. CID in the electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) modes has been found to generate mostly even-electron fragment ions while it has been occasionally reported to form odd-electron free radical ions. However, the structural requirements and the fragmentation mechanisms for free-radical CIDs have not been well characterized in the literature. For this purpose, we studied a series of aromatic and non-aromatic compounds such as sulfonamides, N-aryl amides, tert-butyl-substituted aromatic compounds, aryl alkyl ethers, and O-alkyl aryl oximes using the LTQ and LTQ Orbitrap linear ion trap mass spectrometers. The accurate measurement of the fragment ion masses established the unambiguous assignment of the fragment structures resulting from the test compounds. Our results showed that free radical fragmentation is structure dependent and is to a large extent correlated with the neighboring groups in the structures that stabilize the newly formed free radical ions. Copyright 2010 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20049883     DOI: 10.1002/rcm.4393

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  7 in total

1.  N-centered odd-electron ions formation from collision-induced dissociation of electrospray ionization generated even-electron ions: single electron transfer via ion/neutral complex in the fragmentation of protonated N,N'-dibenzylpiperazines and protonated N-benzylpiperazines.

Authors:  Yunfeng Chai; Hezhi Sun; Yuanjiang Pan; Cuirong Sun
Journal:  J Am Soc Mass Spectrom       Date:  2011-06-22       Impact factor: 3.109

2.  Low-energy collision-induced dissociation mass spectra of protonated p-toluenesulfonamides derived from aliphatic amines.

Authors:  Jason B Bialecki; Carl S Weisbecker; Athula B Attygalle
Journal:  J Am Soc Mass Spectrom       Date:  2014-03-28       Impact factor: 3.109

3.  Mass spectrometry and theoretical studies on N-C bond cleavages in the N-sulfonylamidino thymine derivatives.

Authors:  Renata Kobetić; Snježana Kazazić; Borislav Kovačević; Zoran Glasovac; Luka Krstulović; Miroslav Bajić; Biserka Žinić
Journal:  J Am Soc Mass Spectrom       Date:  2015-03-12       Impact factor: 3.109

4.  On the origin of the methyl radical loss from deprotonated ferulic and isoferulic acids: electronic excitation of a transient structure.

Authors:  Xiaoping Zhang; Fei Li; Huiqing Lv; Yanqing Wu; Gaofeng Bian; Kezhi Jiang
Journal:  J Am Soc Mass Spectrom       Date:  2013-04-12       Impact factor: 3.109

5.  Elimination of benzene from protonated N-benzylindoline: benzyl cation/proton transfer or direct proton transfer?

Authors:  Cheng Guo; Lei Yue; Mengzhe Guo; Kezhi Jiang; Yuanjiang Pan
Journal:  J Am Soc Mass Spectrom       Date:  2013-01-30       Impact factor: 3.109

6.  Unlocking the Diversity of Pyrroloiminoquinones Produced by Latrunculid Sponge Species.

Authors:  Jarmo-Charles J Kalinski; Rui W M Krause; Shirley Parker-Nance; Samantha C Waterworth; Rosemary A Dorrington
Journal:  Mar Drugs       Date:  2021-01-28       Impact factor: 5.118

7.  Derivatization of bisphenol A and its analogues with pyridine-3-sulfonyl chloride: multivariate optimization and fragmentation patterns by liquid chromatography/Orbitrap mass spectrometry.

Authors:  Jorge Regueiro; Andreas Breidbach; Thomas Wenzl
Journal:  Rapid Commun Mass Spectrom       Date:  2015-08-30       Impact factor: 2.419

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.