NDLI: On the Oxidation of the Three-Dimensional Aromatics $[B_{12}X_{12}]^{2−}$ (X=F, Cl, Br, I)

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On the Oxidation of the Three-Dimensional Aromatics $[B_{12}X_{12}]^{2−}$ (X=F, Cl, Br, I)

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Kacprzak, Sylwia Weber, Stefan Warneke, Jonas Riebau, Rainer Roemmele, Tracey L. Kessler, Mathias Jenne, Carsten Scherer, Harald Vent-schmidt, Thomas Derendorf, Janis Boeré, René T. Rühle, Monika Riedel, Sebastian
Description	Author Affiliation: Boeré RT ( Department of Chemistry and Biochemistry, University of Lethbridge, 4401 University Drive, Lethbridge, Alberta T1K 3M4 (Canada).)
Abstract	The perhalogenated closo-dodecaborate dianions $[B_{12}X_{12}]^{2−}$ (X=H, F, Cl, Br, I) are three-dimensional counterparts to the two-dimensional aromatics $C_{6}X_{6}$ (X=H, F, Cl, Br, I). Whereas oxidation of the parent compounds $[B_{12}H_{12}]^{2−}$ and benzene does not lead to isolable radicals, the perhalogenated analogues can be oxidized by chemical or electrochemical methods to give stable radicals. The chemical oxidation of the closo-dodecaborate dianions $[B_{12}X_{12}]^{2−}$ with the strong oxidizer $AsF_{5}$ in liquid sulfur dioxide $(lSO_{2})$ yielded the corresponding radical anions $[B_{12}X_{12}]^{⋅−}$ (X=F, Cl, Br). The presence of radical ions was proven by EPR and UV/Vis spectroscopy and supported by quantum chemical calculations. Use of an excess amount of the oxidizing agent allowed the synthesis of the neutral perhalogenated hypercloso-boranes $B_{12}X_{12}$ (X=Cl, Br). These compounds were characterized by single-crystal X-ray diffraction of dark blue $B_{12}Cl_{12}$ and $[Na(SO_{2})_{6}][B_{12}Br_{12}]⋅B_{12}Br_{12}.$ Sublimation of the crude reaction products that contained $B_{12}X_{12}$ (X=Cl, Br) resulted in pure dark blue $B_{12}Cl_{12}$ or decomposition to red $B_{9}Br_{9},$ respectively. The energetics of the oxidation processes in the gas phase were calculated by DFT methods at the PBE0/def2-TZVPP level of theory. They revealed the trend of increasing ionization potentials of the $[B_{12}X_{12}]^{2−}$ dianions by going from fluorine to bromine as halogen substituent. The oxidation of all $[B_{12}X_{12}]^{2−}$ dianions was also studied in the gas phase by mass spectrometry in an ion trap. The electrochemical oxidation of the closo-dodecaborate dianions $[B_{12}X_{12}]^{2−}$ (X=F, Cl, Br, I) by cyclic and Osteryoung square-wave voltammetry in liquid sulfur dioxide or acetonitrile showed very good agreement with quantum chemical calculations in the gas phase. For $[B_{12}X_{12}]^{2−}$ (X=F, Cl, Br) the first and second oxidation processes are detected. Whereas the first process is quasi-reversible (with oxidation potentials in the range between +1.68 and +2.29 V $(lSO_{2},$ versus ferrocene/ferrocenium $(Fc^{0/+}))),$ the second process is irreversible (with oxidation potentials ranging from +2.63 to +2.71 V $(lSO_{2},$ versus $Fc^{0/+})).$ $[B_{12}I_{12}]^{2−}$ showed a complex oxidation behavior in cyclic voltammetry experiments, presumably owing to decomposition of the cluster anion under release of iodide, which also explains the failure to isolate the respective radical by chemical oxidation.
ISSN	09476539
e-ISSN	15213765
Journal	Chemistry - A European Journal
Issue Number	15
Volume Number	20
Language	English
Publisher	Wiley-VCH;ChemPubSoc Europe
Publisher Date	2014-04-07
Publisher Place	Germany
Access Restriction	Open
Subject Keyword	Chemistry
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry Catalysis

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