A Theoretical and Mass Spectrometry Study of Dimethyl Methylphosphonate: New Isomers and Cation Decay Channels in an Intense Femtosecond Laser Field

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 121; no. 44; pp. 8414 - 8424
• Main Authors: Gutsev, G. L, Ampadu Boateng, Derrick, Jena, P, Tibbetts, Katharine Moore
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 09.11.2017
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/acs.jpca.7b08889

Using both mass spectrometry with intense femtosecond laser ionization and high-level computational methods, we have explored the structure and fragmentation patterns of dimethyl methylphosphonate (DMMP) cation. Extensive search of the geometries of both neutral and positively charged DMMP yields new isomers that are appreciably lower in total energy than those commonly synthesized using the Michaelis–Arbuzov reaction. The stability of the standard isomer with CH3PO­(OCH3)2 topology is found to be due to the presence of high barriers to isomer interconversion that involves several transition states. Our femtosecond laser ionization experiments show that the relative yields of the major dissociation products as a function of peak laser intensity correlate well with the theoretical estimates for the energies of the DMMP+ decay via various channels. In contrast, the peak laser intensities required for observation of minor dissociation products exhibit no correlation with the computed decay energies, which suggests that barrier heights and/or excited electronic states of DMMP+ determine its preferred fragmentation pathways in an intense femtosecond laser field.