Multiphoton Ionization and Dissociation of Nitromethane Using Femtosecond Laser Pulses at 375 and 750 nm

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 101; no. 5; pp. 817 - 823
• Main Authors: Kilic, H. S, Ledingham, K. W. D, Kosmidis, C, McCanny, T, Singhal, R. P, Wang, S. L, Smith, D. J, Langley, A. J, Shaikh, W
• Format: Journal Article
• Language: English
• Published: American Chemical Society 30.01.1997
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp962495d

The photochemistry of nitromethane has been studied extensively for many years. Although it is generally agreed that the principal photodissociative process is cleavage of the C−N bond to yield the methyl radical and nitrogen dioxide, there is some evidence of minor competing dissociation channels. A number of different groups have used lasers of different wavelengths, but the results of these studies vary considerably and no clear picture of the minor dissociative channels has yet emerged. The use of femtosecond (fs) duration laser pulses for photoionization of molecules is currently an area of considerable interest, since the process can lead to the efficient production of intact molecular ions. It was felt that femtosecond laser mass spectrometry (FLMS) could provide added information on the dissociation pathways of nitromethane. Laser pulses of 90 fs time duration at wavelengths of 375 and 750 nm, coupled to a time-of-flight mass spectrometer, have been used in this study, and contrary to photoexcitation using nanosecond (ns) pulses, a large parent ion, 61 (CH3NO2 +), is detected together with strong peaks at m/e = 15 (CH3 +), 30 (NO+), 46 (NO2 +) as well as a number of other minor peaks. This fragmentation pattern can be explained by a predominantly ID (ionization followed by dissociation) route.