Role of the solvent on the stability of cycloserine under ESI‐MS conditions. (24th June 2014)

• Record Type: Journal Article
• Authors: Fraschetti, Caterina; Filippi, Antonello; Mannina, Luisa; Sobolev, Anatoly P.; Speranza, Maurizio
• Is Part Of: Journal of mass spectrometry. Volume 49:Number 7(2014:Jul.)
• Page Start: 608
• Page End: 612
• Publication Date: 2014-06-24
• Subjects: Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/jms.3380
• Languages: English
• ISSNs: 1076-5174

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The effects of methanol (M) and acetonitrile (A) on the stability of cycloserine (1) have been studied. InfraRed Multiphoton PhotoDissociation (IRMPD) spectroscopy of the ionic species from electrospray ionization tandem mass spectrometry (ESI‐MS) of 1/M and 1/A solutions points to extensive dimerization of 1 to <italic>cis</italic>‐3, 6‐bis(aminooxymethyl)‐2, 5‐piperidinedione (2), while the same process is not observed in the ESI‐MS of 1/M solutions. 1D and 2D nuclear magnetic resonance experiments confirmed these findings by showing that partial dimerization of 1 actually takes place at room temperature in acetonitrile even before ESI‐MS analysis. Comparison of nuclear magnetic resonance and IRMPD spectroscopic data from the same 1/A solution suggests that dimerization of cycloserine is enhanced in the ESI source. Copyright © 2014 John Wiley &amp; Sons, Ltd.</p> </abstract>