202231
Chromium(III) acetylacetonate
97%
Synonyme(s) :
Chromium(III) 2,4-pentanedionate, Cr(acac)3
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A propos de cet article
Formule linéaire :
Cr(C5H7O2)3
Numéro CAS:
Poids moléculaire :
349.32
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
244-526-0
Beilstein/REAXYS Number:
4148971
MDL number:
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JWORPXLMBPOPPU-LNTINUHCSA-K
InChI
1S/3C5H8O2.Cr/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3-;
SMILES string
CC(=O)\C=C(\C)O[Cr](O\C(C)=C/C(C)=O)O\C(C)=C/C(C)=O
assay
97%
form
solid
reaction suitability
core: chromium
bp
340 °C (lit.)
mp
210 °C (lit.)
Quality Level
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Catégories apparentées
General description
Chromium(III) acetylacetonate (Cr(acac)₃) is a high-purity (≥97%) coordination complex that appears as a purple to very dark purple powder or in chunk form. It is a stable, air-insensitive compound, soluble in non-polar organic solvents. Its high thermal stability and well-defined molecular structure make it an excellent precursor for synthesizing advanced materials. Cr(acac)₃ is especially valued for applications in catalysis, thin film deposition, and as a molecular probe in spectroscopic studies.
Application
Chromium(III) acetylacetonate can be used as:
- A precursor for the synthesis of chromium oxide (Cr₂O₃) nanoparticles, which are utilized in magnetic, catalytic, and electrochemical devices
- A molecular precursor in chemical vapor deposition (CVD) and sol-gel processes to fabricate chromium-containing thin films for electrochromic and energy storage applications
- A catalyst or catalyst precursor in selective oxidation and polymerization reactions, enabling efficient and sustainable organic transformations
Analysis Note
Used to modify the surface properties of solid polyurethanes formed in its presence.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Classe de stockage
11 - Combustible Solids
wgk
WGK 2
flash_point_f
>392.0 °F
flash_point_c
> 200 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Michael E Ziebel et al.
Chemical science, 11(26), 6690-6700 (2020-09-22)
The incorporation of second-row transition metals into metal-organic frameworks could greatly improve the performance of these materials across a wide variety of applications due to the enhanced covalency, redox activity, and spin-orbit coupling of late-row metals relative to their first-row
Ik-Soo Shin et al.
The Analyst, 136(10), 2151-2155 (2011-03-25)
Though recently Ir(III) complexes have attracted much interest in electrochemiluminescent (ECL) analysis due to their high emission in various wavelengths, there were a few studies reported on its analytical applications. In this study, we evaluate the ECL from (pq)(2)Ir(acac) (pq
Gui-Ge Hou et al.
Chemical communications (Cambridge, England), 47(38), 10731-10733 (2011-08-27)
Two NbO-type MOFs based on ditopic pyridyl substituted diketonate ligands were reported. One exhibits a reversible SC-SC water encapsulation, while the other shows an interesting guest-driven luminescent property based on M(III) acetylacetonate (M = Eu and Fe) guest species.
David N Paglia et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 30(12), 1971-1978 (2012-06-02)
This study quantified the effects of local intramedullary delivery of an organic vanadium salt, which may act as an insulin-mimetic on fracture healing. Using a BB Wistar rat femoral fracture model, local vanadyl acetylacetonate (VAC) was delivered to the fracture
Yanfang Li et al.
Dalton transactions (Cambridge, England : 2003), 41(13), 3807-3816 (2012-02-24)
Biscyclometalated iridium(III) complexes with an ancillary acetylacetone ligand, Ir(L)(2)(acac), (L = 2-(benzo[b]thiophen-2-yl)pyridine (btp), 1-phenylisoquinoline (piq), 2-phenylbenzothiazole (bt), 2-phenylpyridine (ppy), acac = deprotonated acetylacetone), demonstrate spectroscopic changes in their UV-Vis absorption and luminescent emission under acidic conditions. Such changes were found
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