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Vibrations in the B4 rhombic structure

Abstract : A double minimum six-dimensional Potential energy surface (PES) is determined in symmetry coordinates for the most stable rhombic (D-2h) B-4 isomer in its (1)A(g) electronic ground state by fitting to energies calculated ab initio. The PES exhibits a barrier to the D-4h square structure of 255 cm(-1). The vibrational levels (J=0) are calculated variationally using an approach which involves the Watson kinetic energy operator expressed in normal coordinates. The pattern of about 65 vibrational levels up to 1600 cm-1 for all stable isotopomers is analyzed. Analogous to the inversion in ammonia-like molecules, the rhombus rearrangements lead to splittings of the vibrational levels. In B-4 it is the B-1g (D-4h mode which distorts the square molecule to its planar rhombic form. The anharmonic fundamental vibrational transitions of B-11(4) are calculated to be (splittings in parentheses): G(O) = 2352(22) cm(-1), v(1)(A(1g)) - 1136(24) cm(-1,) v(2)(B-1g)=209(144) cm(-1) v(3)(B-2g)=1198(19)cm(-1), v(4)(B-2u) = 271(24) cm(-1), and v(5) (E-u) = 1030( 166) cm(-1) (D-4h notation). Their variations in all stable isotoporners were investigated. Due to the presence of strong anharmonic resonances between the B-1g in-plane distortion and the B-2u, out-of-plane bending modes. the hiaher overtones and combination levels are difficult to assign unequivocally.
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https://hal.archives-ouvertes.fr/hal-00712811
Contributor : Roberto Linguerri Connect in order to contact the contributor
Submitted on : Thursday, June 28, 2012 - 11:30:06 AM
Last modification on : Thursday, September 29, 2022 - 2:21:15 PM

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Roberto Linguerri, Isabelle Navizet, P. Rosmus, S. Carter, J. P. Maier. Vibrations in the B4 rhombic structure. Journal of Chemical Physics, 2005, 122 (3), pp.034301. ⟨10.1063/1.1828045⟩. ⟨hal-00712811⟩

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