Competition for Hydride Between Silicon and Boron: Synthesis and Characterization of a Hydroborane-Stabilized Silylium Ion
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Potent main-group Lewis acids are capable of activating element-hydrogen bonds. To probe the rivalry for hydride between silylium- and borenium-ion centers, a neutral precursor with the hydrosilane and hydroborane units in close proximity on a naphthalene-1,8-diyl platform was designed. Abstraction of one hydride leads to a hydroborane-stabilized silylium ion rather than a hydrosilane-coordinated borenium ion paired with [B(C F ) ] or [HCB Cl ] as counteranions. Characterization by multinuclear NMR spectroscopy and X-ray diffraction supported by DFT calculations reveals a cationic, unsymmetrical open three-center, two-electron (3c2e) Si-H-B linkage.
Catalyst-free diboration and silaboration of alkenes and alkynes using bis(9-heterofluorenyl)s.
Gilmer J, Trageser T, caic L, Virovets A, Bolte M, Lerner H Chem Sci. 2023; 14(17):4589-4596.
PMID: 37152266 PMC: 10155929. DOI: 10.1039/d3sc01395b.
Gilmer J, Bolte M, Virovets A, Lerner H, Fantuzzi F, Wagner M Chemistry. 2022; 29(4):e202203119.
PMID: 36210643 PMC: 10100083. DOI: 10.1002/chem.202203119.
Gao H, Muller R, Irran E, Klare H, Kaupp M, Oestreich M Chemistry. 2021; 28(12):e202104464.
PMID: 34918852 PMC: 9303568. DOI: 10.1002/chem.202104464.