Modeling of the structure and IR spectra of boron difluoride acetylacetonate and its halogen-substituted derivatives

Abstract

The infrared spectra of the complexes of boron difluoride acetylacetonate and its halogen-substituted derivatives F2B(aaX) (X = H, Cl, Br, I) in the crystalline state are studied. The substituent effect on the geometry and force field of molecules is revealed from DFT/B3LYP quantum chemical calculations with the 6-311G(d,p) basis set. The detailed assignment of IR absorption bands is performed based on the calculations of normal modes (NMs) and the potential energy distribution (PED). The bands most sensitive to the substituent nature belong to vibrations with prevalent involvement of ring CC and CO bonds and some low-frequency noncharacteristic NMs involving the Х atom. In support of the single crystal XRD data, intermolecular interactions have the strongest effect on the characteristic bands of the BF2 moiety in the ranges 1280-1220 cm–1 and 875-835 cm–1; the sequences of IR band frequency shifts in a series of substituents corresponding to these interactions are reported.