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Diborylated magnesium anthracene as precursor for B2H5(-)-bridged 9,10-dihydroanthracene
Steffen Pospiech1, Michael Bolte1, Hans-Wolfram Lerner1
1J. W. Goethe-Universität, Institut für Anorganische und Analytische Chemie, Max-von-Laue-Straße 7, 60438 Frankfurt (Main) (Germany), Fax: (+49) 69-798-29260.
Abstract:
9,10-(Bpin)2-anthracene (3, HBpin = pinacolborane) was synthesized from 9,10-dibromoanthracene in a stepwise lithiation/borylation sequence. The reaction of 3 with highly activated magnesium furnished the diborylated magnesium anthracene 4, which was quenched in situ with ethereal HCl to yield cis-9,10-(Bpin)2-DHA (cis-5, DHA = 9,10-dihydroanthracene). Compound cis-5, in turn, can be reduced with Li[AlH4] in THF to give its diborate Li2[cis-9,10-(BH3)2-DHA] (Li2 [cis-6]). In the crystal lattice, the THF solvate Li2[cis-6]⋅3 THF establishes a dimeric structure with Li-(μ-H)-B coordination modes. Hydride abstraction from Li2[cis-6] with Me3SiCl yields the B-H-B-bridged DHA Li[7]. This product can also be viewed as a unique cyclic B2H7(-) derivative with a hydrocarbon backbone. Treatment of Li2[cis-6] with the stronger hydride abstracting agent Me3SiOTf (HOTf = trifluoromethanesulfonic acid) in THF affords the THF diadduct of cis-9,10-(BH(OTf))2-DHA.
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