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- W1798356176 abstract "The carbonyl cluster [Ir4(CO)11(SnX3)]− [X = Cl, (1a) or Br (1b)] can be formed in good yield by insertion of SnX2 in the Ir–Br bond of [Ir4(CO)11Br]− or, much less efficiently, by substitution of bromine with [SnCl3]−, in THF at room temperature. The disubstituted cluster [Ir4(CO)10(SnCl3)2]2− (2) was obtained in 50% yields by double substitution on [Ir4(CO)11Br]−, in THF at 60 °C, whereas [Ir6(CO)15(SnCl3)]− (3) can be prepared by carbonyl substitution of the homoleptic complex [Ir6(CO)16] with an excess of [SnCl3]− in refluxing THF. In the three compounds, the SnCl3 units act as a one electron donor, displaying terminal (in 2), edge-bridging (in 1 and 2) and face-bridging (in 3) coordination. In keeping with a reduced bond order, the Ir–Sn bond distances increase in the series, being 2.584(1) Å for a terminal group; 2.72 Å for edge-bringing units and 2.78 Å for the face-bridging SnCl3. Regardless of the coordination mode, the geometry of the three chlorine atoms is always pyramidal, with Cl–Sn–Cl angles close to 90° and Sn–Cl bond distances close to 2.42 Å. Tin is always symmetrically bridging, with Ir–Sn–Ir close to 60°." @default.
- W1798356176 created "2016-06-24" @default.
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- W1798356176 date "2003-01-01" @default.
- W1798356176 modified "2023-10-16" @default.
- W1798356176 title "A coordinatively flexible ligand for carbonyl clusters: bridging and terminal SnCl<sub>3</sub>groups in the iridium clusters [Ir<sub>4</sub>(CO)<sub>11</sub>(μ-SnCl<sub>3</sub>)]<sup>−</sup>, [Ir<sub>4</sub>(CO)<sub>10</sub>(SnCl<sub>3</sub>)(μ-SnCl<sub>3</sub>)]<sup>2−</sup>and [Ir<sub>6</sub>(CO)<sub>15</sub>(μ<sub>3</sub>-SnCl<sub>3</sub>)]<sup>−</sup>" @default.
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- W1798356176 doi "https://doi.org/10.1039/b310790f" @default.
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