TY - JOUR
T1 - Reactivity of Decaborane(14) with Pyridine
T2 - Synthesis and Characterization of the First 6,6-Substituted Isomer of nido-BwHu, 6,6-(C5H5N)2B10H12, and Application of 11B−11B Double-Quantum NMR Spectroscopy
AU - Cendrowski-Guillaume, Sophie M.
AU - O’Loughlin, Jennifer L.
AU - Pelczer, István
AU - Spencer, James T.
PY - 1995/7/1
Y1 - 1995/7/1
N2 - In the low-temperature reaction of B10H14 with C5H5N, a new product, identified as arachno-6,6-(C5H5N)2B10H12, was formed in high yield and purity. The proposed 6,6-L2B10H12 compound represents the first known report of this decaborane substitution pattern. The formation of an asymmetric 6,6-(C5H5N)2B10H12 isomer was unexpected on the basis of literature precedent describing the synthesis and structural elucidation of numerous 6,9-L2B10H12 species (where L = Lewis base). The observed reaction sequence in the formation of the 6,6-(C5H5N)2B10H12 compound proceeded through an initially observed [H·C5H5N]+[B10H13]− intermediate. In addition to the formation of the 6,6-isomer, the synthesis of the 6,9-(C5H5N)2B10H12 isomer is also reported from the reflux of nido-B10H12 in pyridine. Refluxing the 6,6-(pyridine)2B10H12 isomer in pyridine was also found to convert this isomer into the 6,9-isomer. Both isomers were characterized by 11B NMR, FITR, UV-vis, mass spectroscopic, and elemental analyses. The structure of the 6,6-isomer was established by 2D 11B−11B COSY NMR data and by the first application of a pure phase 11B−11B 2Q correlation NMR (double-quantum) experiment to the elucidation of a borane cluster framework. This latter NMR technique was very successful in greatly simplifying the NMR assignments of the 6,6-substituted decaborane cluster species and should be a very powerful tool in cluster structure elucidation in general.
AB - In the low-temperature reaction of B10H14 with C5H5N, a new product, identified as arachno-6,6-(C5H5N)2B10H12, was formed in high yield and purity. The proposed 6,6-L2B10H12 compound represents the first known report of this decaborane substitution pattern. The formation of an asymmetric 6,6-(C5H5N)2B10H12 isomer was unexpected on the basis of literature precedent describing the synthesis and structural elucidation of numerous 6,9-L2B10H12 species (where L = Lewis base). The observed reaction sequence in the formation of the 6,6-(C5H5N)2B10H12 compound proceeded through an initially observed [H·C5H5N]+[B10H13]− intermediate. In addition to the formation of the 6,6-isomer, the synthesis of the 6,9-(C5H5N)2B10H12 isomer is also reported from the reflux of nido-B10H12 in pyridine. Refluxing the 6,6-(pyridine)2B10H12 isomer in pyridine was also found to convert this isomer into the 6,9-isomer. Both isomers were characterized by 11B NMR, FITR, UV-vis, mass spectroscopic, and elemental analyses. The structure of the 6,6-isomer was established by 2D 11B−11B COSY NMR data and by the first application of a pure phase 11B−11B 2Q correlation NMR (double-quantum) experiment to the elucidation of a borane cluster framework. This latter NMR technique was very successful in greatly simplifying the NMR assignments of the 6,6-substituted decaborane cluster species and should be a very powerful tool in cluster structure elucidation in general.
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U2 - 10.1021/ic00119a015
DO - 10.1021/ic00119a015
M3 - Article
AN - SCOPUS:0007242065
SN - 0020-1669
VL - 34
SP - 3935
EP - 3941
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 15
ER -