JOURNAL ARTICLE

Theoretical study of structure, vibrational frequencies, and electronic spectra of polychlorinated dibenzo-p-dioxins

Ivan Ljubić, Aleksandar Sabljić
Journal of Physical Chemistry. A 2006 April 6, 110 (13): 4524-34
16571059
The structure, vibrational frequencies, and excited states of 2,3,7,8-tetrachloro-, 1,4,6,9-tetrachloro-, and octachlorodibenzo-p-dioxin (2,3,7,8-TCDD, 1,4,6,9-TCDD, and OCDD) were studied via complete active space SCF followed by the multireference second-order perturbative approach (CASSCF/CASPT2), as well as the time-dependent density functional theory (TD-B3LYP). The cc-pVDZ basis set and the full pi-electron active spaces of 16 electrons in 14 active orbitals were employed. Whereas 2,3,7,8-TCDD assumes a planar D(2)(h)() minimum, 1,4,6,9-TCDD and OCDD are slightly folded exhibiting the C(2)(v)() symmetry. The extra stabilization due to the folding is very small. In all three isomers the highly intensive band system in the 200-240 nm region is dominated by the transitions to the 2(1)B(2u) and 3(1)B(2u) states with by far the largest oscillator strengths. The low-intensity absorptions in the 280-320 nm region can be attributed to the 1(1)B(2u) <-- 1(1)A(g), with possible contribution of the vibronically allowed 2(1)A(g) <-- 1(1)A(g) transition. Both CASPT2 and TD-B3LYP convincingly predict 1(3)B(3g) to be the lowest lying triplet state, which contradicts the experimental assignments. Calculated harmonic wavenumbers and absorption spectra agree well with the experimental data, and are sufficiently distinct to allow for an unambiguous identification of the three isomers.

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