Is there a transition state for the unimolecular dissociation of cyclotetraoxygen (O4) ?

• Published in: The Journal of chemical physics 1992-01, Vol.96 (2), p.1176-1182
• Main Authors: SEIDL, E. T, SCHAEFER, H. F
• Format: Article
• Language: English
• Subjects: Atomic and molecular physics; Electron correlation calculations for atoms and molecules; Electronic structure of atoms, molecules and their ions: theory; Exact sciences and technology; Physics
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.462205

The cyclo-O4 molecule is isoelectronic with cyclobutane and has been mentioned as a potential new high energy density material (HEDM). The important unresolved question has been whether or not cyclo-O4 is a genuine minimum on the O4 potential energy hypersurface. Here the transition state for cyclo-O4 dissociation to two O2 molecules has been located at a number of levels of theory using a double zeta plus polarization (DZP) basis set. The theoretical methods with which the transition state geometry was optimized include two-configuration self-consistent-field (TCSCF), configuration interaction including all single and double excitations (CISD), coupled cluster including all single and double excitations (CCSD), and the latter with a noniterative correction for connected triple excitations, CCSD(T). The equilibrium geometry of O4 has D2d symmetry, while a stationary point of D2 symmetry is of Hessian index two (i.e., two imaginary vibrational frequencies) at the highest level of theory, DZP CCSD(T). The true transition state lies only slightly lower energetically (classical barrier 7.9 kcal/mole) and is of C2 symmetry with the DZP CCSD(T) method. The activation energy was predicted in a completely consistent manner to be 6.2 kcal/mole. The possibility that this barrier could disappear entirely at higher levels of theory is discussed. It is concluded that the O4 barrier is too low for O4 to be useful as a HEDM.