<p>Treatment of [Os<sub>3</sub>(CO)<sub>10</sub>(µ-H)(µ-N, O-sac)] (<i>sac</i> = saccharinate) with triphenylphosphine selenide (Ph<sub>3</sub>PSe) in boiling toluene (110&#xa0;°C) furnishes the selenido-capped triosmium cluster [Os<sub>3</sub>(CO)<sub>6</sub>(µ-H)(PPh<sub>3</sub>)<sub>2</sub>(µ-N, O-sac)(µ<sub>3</sub>-Se)<sub>2</sub>] (<b>1</b>) in low yield (21%). Cluster <b>1</b> possesses two capping selenido and two PPh<sub>3</sub> ligands, as confirmed by the crystal structure determined using single-crystal XRD analysis. It crystallizes in the P-1 triclinic system with two crystallographically independent molecules in the asymmetric unit, representing isomeric forms of <b>1</b>, which is also observed in solution. DFT calculations have been performed to confirm the bonding in both these isomers (<b>1a</b> and <b>1b</b>) and to determine their relative energies.</p> Graphical Abstract <p></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Reaction of the Saccharinate (sac)-bridged Triosmium [Os3(CO)10(µ-H)(µ-N, O-sac)] with Ph3PSe: Synthesis, Crystal and Electronic Structures of the Two Isomers of [Os3(CO)6(µ-H)(PPh3)2(µ-N, O-sac)(µ3-Se)2]

  • Md. Masud Rana,
  • Mithun Chandra Sarker,
  • Vladimir N. Nesterov,
  • German E. Pieslinger,
  • Shishir Ghosh

摘要

Treatment of [Os3(CO)10(µ-H)(µ-N, O-sac)] (sac = saccharinate) with triphenylphosphine selenide (Ph3PSe) in boiling toluene (110 °C) furnishes the selenido-capped triosmium cluster [Os3(CO)6(µ-H)(PPh3)2(µ-N, O-sac)(µ3-Se)2] (1) in low yield (21%). Cluster 1 possesses two capping selenido and two PPh3 ligands, as confirmed by the crystal structure determined using single-crystal XRD analysis. It crystallizes in the P-1 triclinic system with two crystallographically independent molecules in the asymmetric unit, representing isomeric forms of 1, which is also observed in solution. DFT calculations have been performed to confirm the bonding in both these isomers (1a and 1b) and to determine their relative energies.

Graphical Abstract