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Issue 3, 2013
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B–N bond formation at stanna-closo-dodecaborate

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Abstract

The heteroborate stanna-closo-dodecaborate shows double substitution in the reaction with alkylated acetonitrile. The reaction product, the charge compensated E,E-isomer, was isomerized into the Z,Z-isomer and hydrogenated at the double bonds. Furthermore the methylated cluster shows less reactivity and the monosubstituted cluster was isolated. The reaction products were characterized by elemental analysis and NMR spectroscopy. Three of the substitution products were also characterized by single crystal structure analysis.

Graphical abstract: B–N bond formation at stanna-closo-dodecaborate

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Publication details

The article was received on 01 Aug 2012, accepted on 15 Oct 2012 and first published on 31 Oct 2012


Article type: Paper
DOI: 10.1039/C2DT31749D
Citation: Dalton Trans., 2013,42, 753-758
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    B–N bond formation at stanna-closo-dodecaborate

    T. Wütz, S. Fleischhauer and L. Wesemann, Dalton Trans., 2013, 42, 753
    DOI: 10.1039/C2DT31749D

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