Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

11-1995

Journal or Book Title

Journal of Chemical Physics

Volume

103

Issue

18

First Page

7983

Last Page

7989

DOI

10.1063/1.470216

Abstract

The potential energy surfaces for the N3F molecule have been studied using multiconfigurational wave functions. Two new isomers were found, one on the singlet (1 A′) and one on the triplet (3 A″) surface. Both isomers have a three‐membered cyclic structure and C ssymmetry. The singlet cyclic isomer is endoergic relative to the open fluorine azide by 15–17 kcal/mol. Its kinetic stability is close to the stability of the open isomer: the barrier separating the cyclic isomer from the dissociation products N2(X1Σ+ g )+NF(a1Δ) is about 13–17 kcal/mol and is lower than the barrier to isomerization. The triplet cyclic isomer is much higher in energy (about 70 kcal/mol), with a barrier to dissociation to N2(X1Σ+ g )+NF(X3Σ) on the order of 15 kcal/mol. Crossings of the 1 A′ and the 3 A″ surfaces may allow the cyclic singlet isomer to predissociate to the ground state products, N2(X1Σ+ g )+NF(X3Σ). It is shown, however, that the singlet–triplet surface of intersection lies ‘behind’ the barrier to singlet decomposition, so that spin‐forbidden predissociation will not preclude detection of cyclic N3F.

Comments

The following article appeared in Journal of Chemical Physics 103 (1995): 7983 and may be found at http://dx.doi.org/10.1063/1.470216.

Rights

Copyright 1995 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics.

Copyright Owner

American Institute of Physics

Language

en

File Format

application/pdf

Included in

Chemistry Commons

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