Abstract

Ab initio calculations determining structures and stabilities of the tetranitrogen N4•+/N4 system and mass spectrometric experiments were carried out in an attempt to understand the processes occurring in a recent neutralization−reionization mass spectrometric (NRMS) experiment starting from a linear N4•+ radical cation (Cacace et al. Science, 2002, 295, 480). Calculations were performed using RCCSD(T) and MRCISD+Q methods with the 6-311+G(3df) basis set. The most stable bound tetranitrogen molecule is an azidonitrene (N3−N) featuring a triplet 3A‘ ‘ ground state and being 56 kJ/mol below the singlet tetrahedral Td isomer. The singlet azidonitrene has an open-shell 1A‘ ‘ state and the corresponding singlet−triplet energy gap amounts to 69 kJ/mol. In both states, fragmentation giving two N2 moieties needs to overcome a barrier height of about 55 kJ/mol. A remarkable difference between N4 isomers is that ionization of triplet azidonitrene leads to the linear 2Σ ground-state radical cation, whereas removal of an electron from singlet tetrahedrane (N4, Td) gives rise to a cyclic three-membered ring belonging to a Π-type excited state. The standard heats of formation are evaluated as follows: Δ (triplet azidonitrene) = 714 ± 20 kJ/mol, Δ (singlet azidonitrene) = 783 ± 20 kJ/mol, Δ (N4, Td) = 770 ± 20 kJ/mol, and Δ (N4•+) = 1398 ± 20 kJ/mol. The adiabatic ionization energies are estimated as IEa (triplet azidonitrene) = 7.3 ± 0.3 eV and IEa (N4, Td) = 10.4 ± 0.3 eV. When repeating the NRMS experiments using our tandem mass spectrometer and operating conditions, the collisional activation (CA) spectrum of N4•+ could be recorded, whereas we could not reproduce the neutralization−reionization spectrum reported by Cacace et al. These results suggest that although azido-nitrene was apparently generated in NRMS experiments, only a very small fraction of the N4 neutral could effectively be reionized, and the resulting spectra could not be reproduced easily, when changing even slightly the experimental conditions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.