C87851
Copper(II) acetylacetonate
97%
동의어(들):
2,4-Pentanedione copper(II) derivative, Bis(2,4-pentanedionato)copper(II), Cu(acac)2, Cupric acetylacetonate
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모든 사진(4)
About This Item
Linear Formula:
Cu(C5H7O2)2
CAS Number:
Molecular Weight:
261.76
Beilstein:
4157957
EC Number:
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23
추천 제품
Quality Level
분석
97%
양식
powder
반응 적합성
core: copper
reagent type: catalyst
mp
284-288 °C (dec.) (lit.)
SMILES string
CC(=O)\C=C(\C)O[Cu]O\C(C)=C/C(C)=O
InChI
1S/2C5H8O2.Cu/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;
InChI key
QYJPSWYYEKYVEJ-FDGPNNRMSA-L
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일반 설명
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.
애플리케이션
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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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
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)
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
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
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
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