Backbone-controlled LUMO energy induces intramolecular C–H activation in ortho-bis-9-borafluorene-substituted phenyl and o-carboranyl compounds leading to novel 9, 10-diboraanthracene derivatives. Issue 47 (23rd November 2022)

• Record Type: Journal Article
• Authors: Krebs, Johannes; Häfner, Alena; Fuchs, Sonja; Guo, Xueying; Rauch, Florian; Eichhorn, Antonius; Krummenacher, Ivo; Friedrich, Alexandra; Ji, Lei; Finze, Maik; Lin, Zhenyang; Braunschweig, Holger; Marder, Todd B.
• Is Part Of: Chemical science. Volume 13:Issue 47(2022)
• Page Start: 14165
• Page End: 14178
• Publication Date: 2022-11-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d2sc06057d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : The backbone linker for two ortho -bis-(9-borafluorene)s influences the LUMO at the boron centers and the reactivity of the respective compounds. Abstract : The choice of backbone linker for two ortho -bis-(9-borafluorene)s has a great influence on the LUMO located at the boron centers and, therefore, the reactivity of the respective compounds. Herein, we report the room temperature rearrangement of 1, 2-bis-(9-borafluorenyl)- ortho -carborane, C2 B10 H10 -1, 2-[B(C12 H8 )]2 ([2a] ) featuring o -carborane as the inorganic three-dimensional backbone and the synthesis of 1, 2-bis-(9-borafluorenyl)benzene, C6 H4 -1, 2-[B(C12 H8 )]2 (2b ), its phenylene analog. DFT calculations on the transition state for the rearrangement support an intramolecular C–H bond activation process via an SE Ar-like mechanism in [2a], and predicted that the same rearrangement would take place in 2b, but at elevated temperatures, which indeed proved to be the case. The rearrangement gives access to 3a and 3b as dibora-benzo[ a ]fluoroanthene isomers, a form of diboron polycyclic aromatic hydrocarbon (PAH) that had yet to be explored. The isolated compounds 2b, 3a, and 3b were fully characterized by NMR, HRMS, cyclic voltammetry (CV), single-crystal X-ray diffraction analysis, and photophysical measurements, supported by DFT and TD-DFT calculations.