Abstract
A novel polyhedral borane cluster, {[η5-C5H5)Fe(η5-C 5H4CH2(Me)3N)]+2 [B22H22]2-} (1), was synthesized in 60% yield from the oxidative coupling reaction involving [B11H14]- ions in a mixed aqueous and organic media. The single crystal X-ray diffraction analysis of 1 showed it to be a fused polyhedron in which an open (nido) decaborane cage is fused to a closed (closo) dodecaborane cluster by eliminating two bridging hydrogens on the B10-cage and two terminal hydrogens on the B12-cluster.
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CITATION STYLE
Hosmane, N. S., Franken, A., Zhang, G., Srivastava, R. R., Smith, R. Y., & Spielvogel, B. F. (1998). Synthesis and crystal structure of a novel fused polyhedral borane dianion, [B22H22]2-: Potential precursor for use in boron neutron capture therapy (BNCT) of cancer. Main Group Metal Chemistry, 21(6), 319–324. https://doi.org/10.1515/MGMC.1998.21.6.319
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