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| (Pentamethylcyclopentadienyl)iridium(III) chloride dimer Basic information | Reaction |
| (Pentamethylcyclopentadienyl)iridium(III) chloride dimer Chemical Properties |
Melting point | 245 °C (decomp)(Solv: chloroform (67-66-3); hexane (110-54-3)) | storage temp. | Inert atmosphere,Room Temperature | solubility | Chloroform (Sparingly), Methanol (Slightly) | form | crystal | color | orange | Stability: | Moisture Sensitive | CAS DataBase Reference | 12354-84-6 |
| (Pentamethylcyclopentadienyl)iridium(III) chloride dimer Usage And Synthesis |
Reaction |
- Iridium-catalyzed C-3 alkylation of oxindole with alcohols.
- Precursor to N-heterocyclic carbene catalyst effective for hydrogenation and alkylation of amines and alcohols.
- Precursor to efficient phosphine free catalyst for enantioselective hydrogenation of quinoline derivatives.
- Catalyst for oxidative C–H activation.
- Precursor to an effective water oxidation catalyst.
| Chemical Properties | orange fine crystalline powder | Uses | Dichloro(pentamethylcyclopentadienyl)iridium(III) dimer is used as a precursor to catalysts for the asymmetric transfer hydrogenation of ketones. It is a catalyst for greener amine synthesis. | General Description | This product has been enhanced for catalytic efficiency. |
| (Pentamethylcyclopentadienyl)iridium(III) chloride dimer Preparation Products And Raw materials |
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