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Copper(II) hexafluoroacetylacetonate
[CAS# 14781-45-4]

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Complete supplier list of Copper(II) hexafluoroacetylacetonate
Identification
Classification Organic raw materials >> Organometallic compound >> Organic copper
Name Copper(II) hexafluoroacetylacetonate
Synonyms Bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)copper (II); Bis(1,1,1,5,5,5-hexafluoroacetylacetonato)copper(II); Bis(hexafluoroacetoacetonato)copper(II); Bis(hexafluoroacetylacetonato)copper; Bis(hexafluoroacetylacetonato)copper(II)
Molecular Structure CAS # 14781-45-4, Copper(II) hexafluoroacetylacetonate, Bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)copper (II), Bis(1,1,1,5,5,5-hexafluoroacetylacetonato)copper(II), Bis(hexafluoroacetoacetonato)copper(II), Bis(hexafluoroacetylacetonato)copper, Bis(hexafluoroacetylacetonato)copper(II)
Molecular Formula C10H2CuF12O4
Molecular Weight 477.65
CAS Registry Number 14781-45-4
EC Number 238-850-1
SMILES C(=C(\O)/C(F)(F)F)\C(=O)C(F)(F)F.C(=C(\O)/C(F)(F)F)\C(=O)C(F)(F)F.[Cu]
Properties
Melting point 120-124 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319-H332-H335    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H332
Eye irritationEye Irrit.2H319
SDS Available
up Discovory and Applicatios
Copper(II) hexafluoroacetylacetonate is a chemical compound with significant importance in coordination chemistry and various industrial applications. This compound features a copper(II) ion coordinated with hexafluoroacetylacetonate ligands, which imparts distinctive properties to the complex.

The discovery of Copper(II) hexafluoroacetylacetonate can be traced back to studies aimed at exploring the coordination chemistry of copper with novel ligands. The hexafluoroacetylacetonate (hfac) ligand is known for its strong electron-withdrawing properties due to the presence of fluorine atoms. This property enhances the stability of the copper(II) center in the complex and modifies its reactivity compared to other copper(II) complexes.

Copper(II) hexafluoroacetylacetonate is synthesized through the reaction of copper(II) salts with hexafluoroacetylacetone in the presence of a suitable base. The resulting complex is characterized by its coordination environment, where the copper(II) ion is surrounded by the hexafluoroacetylacetonate ligands in a square planar arrangement. This geometric configuration is typical for copper(II) complexes and contributes to the compound’s stability and reactivity.

One of the primary applications of Copper(II) hexafluoroacetylacetonate is in the field of catalysis. The compound acts as a catalyst in various organic transformations, including oxidation and coupling reactions. Its role as a catalyst is attributed to the ability of the copper(II) center to participate in redox processes, facilitating the formation of new chemical bonds. The electron-withdrawing effect of the hexafluoroacetylacetonate ligands further enhances the catalytic activity by stabilizing reaction intermediates.

In material science, Copper(II) hexafluoroacetylacetonate is utilized in the preparation of copper-containing thin films and coatings. The compound is employed in chemical vapor deposition (CVD) processes to deposit copper-based materials onto substrates. These copper films and coatings have applications in electronics, where they are used as conductive layers in various devices. The stability of the complex and the volatility of the hexafluoroacetylacetonate ligands make it suitable for CVD processes, providing a reliable source of copper for thin film deposition.

Additionally, Copper(II) hexafluoroacetylacetonate is used in the synthesis of other copper-containing compounds and materials. It serves as a precursor for the preparation of copper-based catalysts, pigments, and other specialty chemicals. The versatility of the compound in forming various copper complexes and materials highlights its importance in both academic research and industrial applications.

Overall, Copper(II) hexafluoroacetylacetonate stands out as a valuable compound in coordination chemistry and catalysis. Its unique properties, including the electron-withdrawing effect of the hexafluoroacetylacetonate ligands and its stability, make it a key player in various chemical processes and applications. The compound’s discovery and subsequent applications underscore its significance in advancing both fundamental chemistry and industrial technology.
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