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Carbene-Stabilized Beryllium Borohydride

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posted on 2012-06-20, 00:00 authored by Robert J. Gilliard, Mariham Y. Abraham, Yuzhong Wang, Pingrong Wei, Yaoming Xie, Brandon Quillian, Henry F. Schaefer, Paul v. R. Schleyer, Gregory H. Robinson
The reaction of N-heterocyclic carbene, L:, with BeCl2 quantitatively yields L:BeCl2 1 (L: = :C­{N­(2,6-Pri2C6H3)­CH}2). The carbene-stabilized beryllium borohydride monomer L:Be­(BH4)2 2 is prepared by the reaction of 1 with LiBH4. Compound 3, prepared by the reaction of 2 with Na2[Fe­(CO)4]·dioxane, represents an unusual “dual reduction” of the imidazole ring (i.e., hydroboration of the CC backbone and hydrogenation of the C2 carbene center).

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