Abstract <p>Treatment of <i>o</i>-carborane with <i>n</i>-butyllithium, sulfur and CpCo(CO)I<sub>2</sub> in CH<sub>2</sub>Cl<sub>2</sub> at room temperature gives the half-sandwich 16e carborane complex CpCo[S<sub>2</sub>C<sub>2</sub>B<sub>10</sub>H<sub>10</sub>], which reacts with PPh<sub>2</sub>Me, PPhMe<sub>2</sub>, PMe<sub>3</sub> to afford addition products CpCo[S<sub>2</sub>C<sub>2</sub>B<sub>10</sub>H<sub>10</sub>]PPh<sub>2</sub>Me (<b>I</b>), CpCo[S<sub>2</sub>C<sub>2</sub>B<sub>10</sub>H<sub>10</sub>]PPhMe<sub>2</sub> (<b>II</b>), CpCo[S<sub>2</sub>C<sub>2</sub>B<sub>10</sub>H<sub>10</sub>]PMe<sub>3</sub>(<b>III</b>), respectively. <b>I</b>, <b>II</b> and <b>III</b> have been characterized by IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, <sup>11</sup>B NMR, elemental analysis, mass spectrum and single-crystal X-ray diffraction analysis (CIF files CCDC nos. 2394909 (<b>I</b>), 2394910 (<b>II</b>), and 2394908 (<b>III</b>)).</p>

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Synthesis and Crystal Structure of the Half-Sandwich Cobalt Complexes Based on 1,2-Dicarba-closo-dodecaborane-1,2-dithiolate Ligand and Trimethylphosphine, Phenyldimethylphosphine, and Diphenylmethylphosphine

  • C. L. Cai,
  • X. H. Fang,
  • H. D. Ye,
  • X. L. Zhang,
  • W. H. Chen,
  • A. X. Zhou,
  • F. Y. Chen,
  • H. N. Peng

摘要

Abstract

Treatment of o-carborane with n-butyllithium, sulfur and CpCo(CO)I2 in CH2Cl2 at room temperature gives the half-sandwich 16e carborane complex CpCo[S2C2B10H10], which reacts with PPh2Me, PPhMe2, PMe3 to afford addition products CpCo[S2C2B10H10]PPh2Me (I), CpCo[S2C2B10H10]PPhMe2 (II), CpCo[S2C2B10H10]PMe3(III), respectively. I, II and III have been characterized by IR, 1H NMR, 13C NMR, 11B NMR, elemental analysis, mass spectrum and single-crystal X-ray diffraction analysis (CIF files CCDC nos. 2394909 (I), 2394910 (II), and 2394908 (III)).