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Macropolyhedral boron-containing cluster chemistry. Aspects of the S2B16H16 system. Preparation, structure, NMR spectroscopy and isomerism
Authors:Pervinder K. Dosangh, Jonathan Bould, Michael G. S. Londesborough, Tom   Jelí  nek, Mark Thornton-Pett, Bohumil tí  br,John D. Kennedy
Affiliation:

a The School of Chemistry of the University of Leeds, Leeds UK LS2 9JT, Northern England, EU, UK

b The Institute of Inorganic Chemistry of the Academy of Sciences of the Czech Republic, 25068, Rez-by-Prague, Czech Republic

Abstract:Thermolysis of [arachno-4-SB8H12] (1) in boiling cyclohexane gives two isomers 2 and 3 of 18-vertex [S2B16H16], together with known 12-vertex [closo-1-SB11H11] (4) and known 11-vertex [nido-7-SB10H12] (5). Compounds 2 and 3 are characterised by single-crystal X-ray diffraction analyses and single- and double-resonance 11B- and 1H-NMR spectroscopy. The [n-S2B16H16] isomer 2 takes the form of nido ten-vertex: nido ten-vertex [anti-B18H22] with the 9 and 9′ positions occupied by S vertices, whereas the [iso-S2B16H16] isomer 3 takes the form of a nido 11-vertex {SB10} subcluster fused via a common two-boron edge to a nido-type {B8} subcluster that is additionally linked exo to the {SB10} subcluster by a bridging S atom that is held endo to the {B8} unit. Isomer 2 is readily deprotonated and its monoanion 6 is characterised by NMR spectroscopy and by a single-crystal X-ray diffraction analysis of its [tmndH]+[n-S2B16H15] salt 6b; deprotonation has occurred from an open-face B---H---B bridging site.
Keywords:NMR spectroscopy   Isomerism   Cyclohexane
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