The molecular structures of pentaborane(9) with halogen substituents in apical and basal positions, determined by electron diffraction and theoretical calculations

Abstract

The molecular structures of 1-bromo–pentaborane(9) and 2-bromo–pentaborane(9) in the gas phase have been determined by electron diffraction and ab initio and DFT computational methods. Computational methods have also been applied to the fluoro and chloro analogues, to 1,2-dibromo-pentaborane(9), and to the parent unsubstituted borane. The electronic effects of halogen substitution on the borane cage are remarkably small, particularly for chlorine and bromine substituents, and steric effects are also minimal, even in the compound with two bromine atoms. The largest effects are (a) lengthening of B_(base)–B_(apex) bonds adjacent to the halogen in the 2-isomers, with an associated shortening of the opposite base–apex bond, (b) shortening of the B_(base)–B_(apex) bond in the 1-fluoro compound, and (c) increase of the B_(base)–B_(apex)–F angle in 1-F–B₅H₈, but a decrease in this angle in the 2-bromo compounds.