Cyclooctadiene iridium chloride dimer
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| Names | |
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| Other names
Bis(1,5-cyclooctadiene)diiridium(I) dichloride
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| Identifiers | |
| ECHA InfoCard | 100.031.961 |
| Properties | |
| C16H24Cl2Ir2 | |
| Molar mass | 671.70 |
| Appearance | red-orange solid |
| Density | 2.65 g/cm3 (red polymorph) |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Cyclooctadiene iridium chloride dimer is an organoiridium compound with the formula Ir2Cl2(C8H12)2, where C8H12 is the diene 1,5-cyclooctadiene. It is an orange solid that is soluble in organic solvents. The complex is used as a precursor to other iridium complexes, some of which are used in homogeneous catalysis. The solid is air-stable but its solutions degrades in air.
The compound is prepared by heating hydrated iridium trichloride and cyclooctadiene in alcohol solvent. In the process, Ir(III) is reduced to Ir(I).
In terms of its molecular structure, the iridium centers are square planar as is typical for a d8 complex. The Ir2Cl2 core is folded with a dihedral angle of 86°. The molecule crystallizes in yellow-orange and red-orange polymorphs; the latter one is more common.
The complex is widely used precursor to other iridium complexes. A notable derivative is Crabtree's catalyst. The chloride ligands can also be replaced to give diiridium complexes exhibiting modified reactivity, e.g. Ir2(OCH3)2(C8H12)2. A closely related but still more reactive complex is chlorobis(cyclooctene)iridium dimer.
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