202231
Chromium(III) acetylacetonate
97%
동의어(들):
Chromium(III) 2,4-pentanedionate, Cr(acac)3
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
Cr(C5H7O2)3
CAS 번호:
Molecular Weight:
349.32
Beilstein:
4148971
EC Number:
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23
Quality Level
분석
97%
양식
solid
반응 적합성
core: chromium
bp
340 °C (lit.)
mp
210 °C (lit.)
SMILES string
CC(=O)\C=C(\C)O[Cr](O\C(C)=C/C(C)=O)O\C(C)=C/C(C)=O
InChI
1S/3C5H8O2.Cr/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3-;
InChI key
JWORPXLMBPOPPU-LNTINUHCSA-K
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일반 설명
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.
애플리케이션
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
분석 메모
Used to modify the surface properties of solid polyurethanes formed in its presence.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
>392.0 °F
Flash Point (°C)
> 200 °C
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Yi Wang et al.
Journal of medicinal chemistry, 56(23), 9601-9611 (2013-11-28)
Current precious-metal-containing anticancer agents are mostly chelated with N-containing ligands and function by interacting with DNA. In the present study, Pd(acac)2, a Pd(II) complex containing four O-donor ligands, has been evaluated as an active anticancer agent. Pd(acac)2 showed no interaction
Gong-Jun Chen et al.
Dalton transactions (Cambridge, England : 2003), 39(44), 10637-10643 (2010-10-06)
Two Eu(III) complexes, [Eu(acac)(3)(dpq)] (1) and [Eu(acac)(3)(dppz)] CH(3)OH (2) {viz. acetylacetonate (acac), dipyrido[3,2-d:20,30-f]quinoxaline (dpq), dipyrido[3,2-a:20,30-c] phenazine (dppz)}, have been synthesized and their DNA binding, photo-induced DNA cleavage activity and cell cytotoxicity are studied. The complexes display significant binding propensity to
The direct writing of plasmonic gold nanostructures by electron-beam-induced deposition.
Katja Höflich et al.
Advanced materials (Deerfield Beach, Fla.), 23(22-23), 2657-2661 (2011-05-04)
Channa R De Silva et al.
Journal of the American Chemical Society, 131(18), 6336-6337 (2009-04-17)
Nearly monodisperse lanthanide-doped magnetite nanoparticles were obtained by thermally decomposing a mixture of Fe(acac)(3) and Ln(acac)(3) (acac = acetylacetonate; Ln = Sm, Eu, Gd) in the presence of passivating surfactants. Magnetic studies revealed room-temperature ferromagnetic behaviors of these doped nanoparticles
Zhan'ao Tan et al.
Physical chemistry chemical physics : PCCP, 14(42), 14589-14595 (2012-09-28)
A solution-processed vanadium oxide (s-VO(x)) anode buffer layer on an indium-tin-oxide (ITO) electrode was used instead of PEDOT:PSS for improving the stability and photovoltaic performance of the polymer solar cells (PSCs). The s-VO(x) layer was prepared by spin-coating a vanadyl
문서
Discover the ways in which high-purity metal salts improve the selectivity, yields, and catalytic efficacy of organic synthesis reactions.
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