Terminal coordination of diatomic boron monofluoride to iron.

Author(s) Drance, M.J.; Sears, J.D.; Mrse, A.M.; Moore, C.E.; Rheingold, A.L.; Neidig, M.L.; Figueroa, J.S.
Journal Science
Date Published 2019 03 15
Abstract

Boron monofluoride (BF) is a diatomic molecule with 10 valence electrons, isoelectronic to carbon monoxide (CO). Unlike CO, which is a stable molecule at room temperature and readily serves as both a bridging and terminal ligand to transition metals, BF is unstable below 1800°C in the gas phase, and its coordination chemistry is substantially limited. Here, we report the isolation of the iron complex Fe(BF)(CO)(CNAr) [Ar, 2,6-(2,4,6-(Pr)CH]CH; -Pr, -propyl], featuring a terminal BF ligand. Single-crystal x-ray diffraction as well as nuclear magnetic resonance, infrared, and Mössbauer spectroscopic studies on Fe(BF)(CO)(CNAr) and the isoelectronic dinitrogen (N) and CO complexes Fe(N)(CO)(CNAr) and Fe(CO)(CNAr) demonstrate that the terminal BF ligand possesses particularly strong σ-donor and π-acceptor properties. Density functional theory and electron-density topology calculations support this conclusion.

DOI 10.1126/science.aaw6102
ISSN 1095-9203
Citation Drance MJ, Sears JD, Mrse AM, Moore CE, Rheingold AL, Neidig ML, et al. Terminal coordination of diatomic boron monofluoride to iron. Science. 2019;363(6432):1203-1205.

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