Abstract or Keywords
Boronic acids are widely used in materials science, pharmacology, and the synthesis of biologically active compounds In this Article, geometrical structures and relative energies of dimers of boroglycine, H2N-CH2-B(OH)(2), and its constitutional isomer H3C-NH-B(OH)(2), were computed using second-order Moller-Plesset perturbation theory and density functional theory; Dunning-Woon correlation-consistent cc-pVDZ, aug-cc-pVDZ, cc-pVTZ, and aug-cc-pVTZ basis sets were employed for the MP2 calculations, and the Pople 6-311++G(d,p) basis set was employed for a majority of the DFT calculations. Effects of an aqueous environment were incorporated into the results using PCM and COSMO-RS methodology. The lowest-energy conformer of the H2N-CH2-B(OH)(2) dimer was a six-membered ring structure (chair conformation; C-i symmetry) with two intermolecular B:N dative-bonds; it was 14.0 kcal/mol lower in energy at the MP2/aug-cc-pVDZ computational level than a conformer with the classic eight-centered ring structure (C-i symmetry) in which the boroglycine monomers are linked by a pair of H-O center dot center dot center dot H bonds. Compared to the results of MP2 calculations with correlation-consistent basis sets, DFT calculations using the PBE1PBE and TPSS functionals with the 6-311++G(d,p) basis set were significantly better at predicting relative conformational energies of the H2N-CH2-B(OH)(2) and H3C-NH-B(OH)(2) dimers than corresponding calculations using the BLYP, B3LYP, OLYP, and O3LYP functionals, particularly with respect to dative-bonded structures.