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(Acetylacetonato)dicarbonyliridium
[CAS# 14023-80-4]

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Identification
ClassificationOrganic raw materials >> Organometallic compound >> Organic iridium
Name(Acetylacetonato)dicarbonyliridium
SynonymsDicarbonylacetylacetonatoiridium(I)
Molecular StructureCAS # 14023-80-4, (Acetylacetonato)dicarbonyliridium
Molecular FormulaC7H7IrO4
Molecular Weight347.35
CAS Registry Number14023-80-4
EC Number621-500-0
SMILESCC(=O)/C=C(/C)O[Ir].[C-]#[O+].[C-]#[O+]
Properties
Melting point>145 °C
Safety Data
Hazard Symbolssymbol symbol   GHS07;GHS08 Warning  Details
Risk StatementsH302-H312-H315-H319-H332-H335-H361  Details
Safety StatementsP203-P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P318-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Reproductive toxicityRepr.2H361
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H332
Specific target organ toxicity - single exposureSTOT SE3H335
SDSAvailable
up Discovery and Applications
(Acetylacetonato)dicarbonyliridium, often referred to as Ir(acac)(CO)2, is an organometallic coordination complex consisting of an iridium center bonded to an acetylacetonate ligand and two carbonyl (CO) groups. In this complex, the iridium is typically in the +1 oxidation state, coordinated in a square planar or slightly distorted geometry, characteristic of low-spin d8 transition metal complexes.

The acetylacetonate (acac) ligand acts as a bidentate chelating ligand, binding to the iridium through two oxygen atoms from the β-diketone functional group. This chelation stabilizes the complex and influences its electronic and steric properties. The two carbonyl ligands bind via their carbon atoms to the iridium center, providing strong metal-to-ligand back-donation, which affects the complex’s reactivity and spectroscopic features.

Synthesis of (acetylacetonato)dicarbonyliridium generally involves the reaction of iridium precursors such as iridium trichloride or dicarbonyl iridium complexes with acetylacetone under controlled conditions. Carbonylation or ligand substitution reactions introduce the carbonyl groups, often performed under CO atmosphere or by using CO-releasing reagents. The product is typically isolated as a crystalline solid, soluble in organic solvents such as dichloromethane or toluene.

This complex is widely used in organometallic chemistry as a catalyst or catalyst precursor. The combination of a stable chelating acac ligand and labile carbonyl groups makes it versatile for catalytic transformations involving hydrogenation, hydroformylation, and carbonylation reactions. The carbonyl ligands can be displaced under reaction conditions, allowing substrate coordination and activation at the metal center.

In addition to catalytic applications, (acetylacetonato)dicarbonyliridium is used in mechanistic studies and synthesis of other iridium complexes. Its well-defined structure facilitates spectroscopic investigations such as infrared and nuclear magnetic resonance spectroscopy, aiding understanding of metal-ligand interactions and electronic properties.

The compound’s stability and reactivity are influenced by the strong chelation of the acac ligand and the π-acceptor ability of the CO ligands. These features make it a useful model compound in exploring the chemistry of iridium carbonyl complexes and their potential in industrial and synthetic applications.

Handling (acetylacetonato)dicarbonyliridium requires standard laboratory safety measures typical for organometallic carbonyl compounds, including use of gloves and fume hoods to avoid exposure to toxic metal complexes and carbon monoxide released under decomposition.

In summary, (acetylacetonato)dicarbonyliridium is a square planar iridium(I) complex coordinated by a bidentate acetylacetonate ligand and two carbonyl ligands. It is synthesized via ligand substitution or carbonylation of iridium precursors and serves as a versatile catalyst precursor and research compound in organometallic chemistry, valued for its stability and reactive carbonyl ligands.

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