Literature DB >> 22002227

Identification of epoxide functionalities in protonated monofunctional analytes by using ion/molecule reactions and collision-activated dissociation in different ion trap tandem mass spectrometers.

Ryan J Eismin1, Mingkun Fu, Sonoeun Yem, Fanny Widjaja, Hilkka I Kenttämaa.   

Abstract

A mass spectrometric method has been delineated for the identification of the epoxide functionalities in unknown monofunctional analytes. This method utilizes gas-phase ion/molecule reactions of protonated analytes with neutral trimethyl borate (TMB) followed by collision-activated dissociation (CAD) in an ion trapping mass spectrometer (tested for a Fourier-transform ion cyclotron resonance and a linear quadrupole ion trap). The ion/molecule reaction involves proton transfer from the protonated analyte to TMB, followed by addition of the analyte to TMB and elimination of methanol. Based on literature, this reaction allows the general identification of oxygen-containing analytes. Vinyl and phenyl epoxides can be differentiated from other oxygen-containing analytes, including other epoxides, based on the loss of a second methanol molecule upon CAD of the addition/methanol elimination product. The only other analytes found to undergo this elimination are some amides but they also lose O = B-R (R = group bound to carbonyl), which allows their identification. On the other hand, other epoxides can be differentiated from vinyl and phenyl epoxides and from other monofunctional analytes based on the loss of (CH(3)O)(2)BOH or formation of protonated (CH(3)O)(2)BOH upon CAD of the addition/methanol elimination product. For propylene oxide and 2,3-dimethyloxirane, the (CH(3)O)(2)BOH fragment is more basic than the hydrocarbon fragment, and the diagnostic ion (CH(3)O)(2)BOH (2) (+) is formed. These reactions involve opening of the epoxide ring. The only other analytes found to undergo (CH(3)O)(2)BOH elimination are carboxylic acids, but they can be differentiated from the rest based on several published ion/molecule reaction methods. Similar results were obtained in the Fourier-transform ion cyclotron resonance and linear quadrupole ion trap mass spectrometer. © American Society for Mass Spectrometry, 2011

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Year:  2011        PMID: 22002227     DOI: 10.1007/s13361-011-0249-y

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  14 in total

1.  A two-dimensional quadrupole ion trap mass spectrometer.

Authors:  Jae C Schwartz; Michael W Senko; John E P Syka
Journal:  J Am Soc Mass Spectrom       Date:  2002-06       Impact factor: 3.109

2.  A neutral loss activation method for improved phosphopeptide sequence analysis by quadrupole ion trap mass spectrometry.

Authors:  Melanie J Schroeder; Jeffrey Shabanowitz; Jae C Schwartz; Donald F Hunt; Joshua J Coon
Journal:  Anal Chem       Date:  2004-07-01       Impact factor: 6.986

3.  Quadrupole ion trap studies of fundamental organic reactions.

Authors:  Scott Gronert
Journal:  Mass Spectrom Rev       Date:  2005 Jan-Feb       Impact factor: 10.946

4.  Phase-modulated stored waveform inverse Fourier transform excitation for trapped ion mass spectrometry.

Authors:  L Chen; T C Wang; T L Ricca; A G Marshall
Journal:  Anal Chem       Date:  1987-02-01       Impact factor: 6.986

5.  Comparison of functional group selective ion-molecule reactions of trimethyl borate in different ion trap mass spectrometers.

Authors:  Steve C Habicht; Nelson R Vinueza; Lucas M Amundson; Hilkka I Kenttämaa
Journal:  J Am Soc Mass Spectrom       Date:  2011-02-01       Impact factor: 3.109

6.  Sites of reaction of pilocarpine.

Authors:  M Satterfield; J S Brodbelt
Journal:  J Am Soc Mass Spectrom       Date:  1999-03       Impact factor: 3.109

7.  Gas phase reactions of trimethyl borate with phosphates and their non-covalent complexes.

Authors:  Scott Gronert; Richard A J O'Hair
Journal:  J Am Soc Mass Spectrom       Date:  2002-09       Impact factor: 3.109

8.  Distinguishing N-oxide and hydroxyl compounds: impact of heated capillary/heated ion transfer tube in inducing atmospheric pressure ionization source decompositions.

Authors:  Dilrukshi M Peiris; Wing Lam; Steven Michael; Ragu Ramanathan
Journal:  J Mass Spectrom       Date:  2004-06       Impact factor: 1.982

9.  Functional group selective ion/molecule reactions: mass spectrometric identification of the amido functionality in protonated monofunctional compounds.

Authors:  Karinna M Campbell; Michael A Watkins; Sen Li; Marc N Fiddler; Brian Winger; Hilkka I Kenttämaa
Journal:  J Org Chem       Date:  2007-03-31       Impact factor: 4.354

10.  Meerwein reaction of phosphonium ions with epoxides and thioepoxides in the gas phase.

Authors:  Eduardo C Meurer; Hao Chen; Leah S Riter; R Graham Cooks; Marcos N Eberlin
Journal:  J Am Soc Mass Spectrom       Date:  2004-03       Impact factor: 3.109

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  2 in total

1.  Identification of Carboxylate, Phosphate, and Phenoxide Functionalities in Deprotonated Molecules Related to Drug Metabolites via Ion-Molecule Reactions with water and Diethylhydroxyborane.

Authors:  Hanyu Zhu; Xin Ma; John Y Kong; Minli Zhang; Hilkka I Kenttämaa
Journal:  J Am Soc Mass Spectrom       Date:  2017-07-24       Impact factor: 3.109

2.  Perspective on Emerging Mass Spectrometry Technologies for Comprehensive Lipid Structural Elucidation.

Authors:  Julia R Bonney; Boone M Prentice
Journal:  Anal Chem       Date:  2021-04-15       Impact factor: 6.986

  2 in total

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