Correlation effects in B1s core-excited states of boronic-acid derivatives: An experimental and computational study.

Abstract

We performed a theoretical investigation on the influence of electronic correlation effects on the B1s NEXAFS spectrum of boronic acid derivatives, namely, boric acid [B(OH)3], phenyl boronic acid (PBA), and 1,4-phenyl diboronic acid (PDBA), employing different computational schemes of increasing complexity, ranging from the purely one-electron scheme based on the transition potential method of density functional theory (DFT-TP), time-dependent DFT (TDDFT), and multiconfigurational self-consistent field (MCSCF). We also report experimental measurements of the B1s NEXAFS spectra of the aforementioned molecules together with the high-resolution C1s NEXAFS spectrum of PBA. We demonstrate that due to the shallow B1s core energy levels compared to C, O, and N, the inclusion of static correlation effects, which can be incorporated by using multireference approaches to excited states, assumes a decisive role in reconciling experiment and theory on B1s core-electron excitation energies and oscillator strengths to valence states. This claim is corroborated by the good agreement that we find between the DFT-TP calculated C1s NEXAFS spectrum and that experimentally measured for PBA and by the failure of both DFT-TP and TDDFT approaches with a selection of xc functionals kernels to properly describe the B1s NEXAFS spectrum of PBA and PDBA, at variance with the good agreement with the experiment that is found by employing the MCSCF wave function approach.