C87851
Copper(II) acetylacetonate
97%
Synonyme(s) :
2,4-Pentanedione copper(II) derivative, Bis(2,4-pentanedionato)copper(II), Cu(acac)2, Cupric acetylacetonate
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A propos de cet article
Formule linéaire :
Cu(C5H7O2)2
Numéro CAS:
Poids moléculaire :
261.76
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
236-477-9
Beilstein/REAXYS Number:
4157957
MDL number:
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QYJPSWYYEKYVEJ-FDGPNNRMSA-L
InChI
1S/2C5H8O2.Cu/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;
SMILES string
CC(=O)\C=C(\C)O[Cu]O\C(C)=C/C(C)=O
assay
97%
form
powder
reaction suitability
core: copper, reagent type: catalyst
mp
284-288 °C (dec.) (lit.)
Quality Level
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Catégories apparentées
General description
Copper(II) acetylacetonate (Cu(acac)2) is an organometallic compound recognized for its low decomposition temperature of 286 °C, making it an ideal precursor for the synthesis of copper and copper oxide nanoparticles. It can be used in electronics, ceramics, and catalysis.
Application
- Dextromethorphan as a moderator of reward deficiency: Research explored Dextromethorphan′s role in moderating reward deficiency associated with serotonin transporter availability in MDMA-treated animals, indicating its potential application in neuropsychopharmacology and addiction studies (Chiu et al., 2024).
- Pharmacotherapies targeting GABA-Glutamate neurotransmission: A review discussed the use of Dextromethorphan among pharmacotherapies targeting GABA-glutamate neurotransmission for treatment-resistant depression, highlighting its role as an NMDA receptor antagonist and sigma-1 receptor agonist (Vecera et al., 2023).
- Experience-dependent psychological effects: A double-blind study compared the psychological effects of Dextromethorphan and Psilocybin in healthy volunteers, examining their experience-dependent and enduring impacts, relevant in clinical psychology and psychedelic research (Mathai et al., 2023).
Copper(II) acetylacetonate can be used as:
- a precursor to synthesize copper based chalcogenides Cu2NiSnS4 CNTS nanocrystals, which are then combined with gold nanoparticles (Au NPs) to form the core-shell structure. Resulting Au/CNTS nanocrystals serve as photoactive materials in hybrid photodetectors, demonstrating superior optoelectronic performance, such as high responsivity and specific detectivity in the visible light spectrum.
- a precursor in the synthesis of Cu-Ga-Zn-S nanorods through a high-temperature injection method, for efficient photocatalytic water splitting.
- a copper precursor in the one-pot synthesis of the core/shell PtCu nanoparticles. These bimetallic PtCu nanoparticles exhibit higher activity in catalyzing the oxygen reduction reaction.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Zofia Kowalewska et al.
Talanta, 103, 66-74 (2012-12-04)
The aim of this work was to investigate the influence of magnesium acetylacetonate (MgA) on the signal of organic forms of vanadium in xylene solution by graphite furnace atomic absorption spectrometry. MgA alone or mixed with palladium acetylacetonate (PdA) was
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
Nan Tian et al.
Dalton transactions (Cambridge, England : 2003), 39(37), 8613-8615 (2010-08-19)
The design, synthesis, photophysical and significantly improved electrooptical properties of a series of red emitting cyclometalated iridium(iii) complexes containing carbazolyl-acetylacetonate ligands are described.
S S Arandjelovic et al.
Journal of B.U.ON. : official journal of the Balkan Union of Oncology, 14(2), 271-279 (2009-08-04)
To investigate the antitumor activity of two newly synthesized ruthenium(III) [Ru(III)] compounds carrying bidentate ligands: (acac)-acetylacetonate, [Ru(acac)3), and (tfac)-trifluoroacetylacetonate [Ru(tfac)3]. The activity of ruthenium(III) analogues was evaluated on HeLa, B16, and Femx cell lines for cytotoxicity in vitro using MTT
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
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