Electrospray tandem mass spectrometry of 2H-chromenes

• Published in: Rapid communications in mass spectrometry 2004-01, Vol.18 (24), p.2969-2975
• Main Authors: Domingues, M. Rosário M., Domingues, Pedro, Oliveira, M. Manuel, Carvalho, Luis H. M., Oliveira-Campos, Ana F., Ferrer Correia, António J.
• Format: Article
• Language: English
• ISSN: 0951-4198; 1097-0231
• DOI: 10.1002/rcm.1713

Several 2H‐chromenes derived from carbazoles were analyzed by electrospray tandem mass spectrometry. The 2H‐chromenes constitute an important class of compounds that exhibit photochromic activity. The fragmentation pathways of the protonated molecular species [M+H]+ were studied, and main fragmentation pathways of these compounds were identified. Fragmentation pathways of [M+D]+ ions were also studied in order to obtain information about the location of the ionizing proton or deuteron. It was found that the proton is not preferentially located on the nitrogen atom. The charge is preferentially located as a tertiary carbocation, resulting from the uptake of the proton (or deuteron) by the zwitterionic open structure of the chromenes. The major fragmentation occurred by cleavage of the γ‐bond relative to the carbocation center, leading to a fragment at m/z 191 (C5H 11+ or C14H9N+), which are the most abundant fragment ions for almost all compounds. The presence of substituents in the chromene ring does not change this behavior. Other observed common fragmentation pathways included loss of CH 3. (15 Da), loss of CO (28 Da), combined loss of CO and CH3 (43 Da), and loss of the phenyl ring via combined loss of C6H4 and CH 3. (−91 Da) and combined loss of C6H6 and CO (−106 Da). Copyright © 2004 John Wiley & Sons, Ltd.