Journal article

Hydroxyl radical formation in the gas phase oxidation of distonic 2-methylphenyl radical cations

MB Prendergast, PA Cooper, BB Kirk, G Da Silva, SJ Blanksby, AJ Trevitt

Physical Chemistry Chemical Physics | Published : 2013

Abstract

The reactions of distonic 4-(N,N,N-trimethylammonium)-2-methylphenyl and 5-(N,N,N-trimethylammonium)-2-methylphenyl radical cations (m/z 149) with O 2 are studied in the gas phase using ion-trap mass spectrometry. Photodissociation (PD) of halogenated precursors gives rise to the target distonic charge-tagged methylphenyl radical whereas collision-induced dissociation (CID) is found to produce unreactive radical ions. The PD generated distonic radicals, however, react rapidly with O2 to form [M + O2]•+ and [M + O2 - OH]•+ ions, detected at m/z 181 and m/z 164, respectively. Quantum chemical calculations using G3SX(MP3) and M06-2X theories are deployed to examine key decomposition pathways of..

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University of Melbourne Researchers

Grants

Awarded by Australian Research Council


Awarded by Centre of Excellence For Free Radical Chemistry and Biotechnology


Funding Acknowledgements

The authors are grateful for the financial support of the Australian Research Council through the Discovery program (SJB: DP0986738; AJT and GdS: DP 130100862; GdS: DP110103889) and Centre of Excellence For Free Radical Chemistry and Biotechnology (CE0561607). The authors also acknowledge the generous allocation of computing resources by the NCI National Facility (Canberra, Australia) under Merit Allocation Scheme.