Monosubstituted Phenylboronic Acids, R–B(OH)2 (R = C6H5, C6H4CH3, C6H4NH2, C6H4OH, and C6H4F): A Computational Investigation View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-08

AUTHORS

Niny Z. Rao, Joseph D. Larkin, Charles W. Bock

ABSTRACT

Phenylboronic acids (PBAs) are an important class of compounds with diverse applications in synthetic, biological, medicinal, and materials chemistry. In this investigation we report structural and thermochemical parameters for several monosubstituted ortho, meta, and para PBAs, R-B(OH)2 (R = C6H5, C6H4CH3, C6H4NH2, C6H4OH, and C6H4F). Equilibrium geometries of all the PBAs discussed in this article were obtained using second-order Møller-Plesset perturbation theory (MP2) with the Dunning-Woon aug-cc-pVDZ basis set; heats of formation (HOF) were calculated at the Gaussian-3 (G3) level of theory. The endo-exo conformers of all the positional isomers of these PBAs were lowest in energy. Using HOF for the monosubstituted PBAs calculated at the G3 level of theory, in conjunction with the experimental HOF for benzene, toluene, aniline, phenol, and fluorobenzene, the values of [Formula: see text] for the transfer processes C6H6 + C6H4X-B(OH)2 → C6H5X + C6H5-B(OH)2 (X = CH3, NH2, OH, and F) are found to be in good agreement with values of [Formula: see text] calculated at the MP2(FC)/aug-cc-pVTZ//MP2(FC)/aug-cc-pVTZ computational level; the bonding in the reactants and products for these transfer reactions are well-matched and thermochemical calculations at this level are expected to be very accurate, providing checks on the G3 HOF calculations. More... »

PAGES

945-955

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11224-016-0897-4

DOI

http://dx.doi.org/10.1007/s11224-016-0897-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047902726

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29375238


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