0102030405
0102030405
Hexafluoroacetylacetone (HFA)
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Contact usPhysical and chemical properties
| Chemical formula | C5H2F6O2 | |||
| Molar mass | 208.06 g/mol | |||
| Appearance | colourless liquid | |||
| Density | 1.47 g/mL | |||
| Boiling point | 70 to 71 °C (158 to 160 °F; 343 to 344 K) |
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| Solubility in water | organic solvents | |||
product description
Hexafluoroacetylacetone (HFA or hfac) is a key β-diketone compound widely used in various fields due to its unique chemical properties, such as strong electron-withdrawing effects, high volatility, and excellent chelating ability. Its major applications include:
1. Organometallic Chemistry & Materials Science
- Precursor Compounds:
Metal complexes of HFA (e.g., Cu(hfac)₂, Pt(hfac)₂) are commonly used in **chemical vapor deposition (CVD)** and **atomic layer deposition (ALD)** to produce thin metal films (e.g., copper, platinum, nickel) for semiconductors, nanomaterials, and conductive coatings.
- Volatile Complexes:
These metal chelates exhibit low-temperature volatility, making them ideal for high-purity metal synthesis.
2. Electronics Industry
- Etching & Cleaning Agents:
HFA derivatives (e.g., cobalt hexafluoroacetylacetonate) serve as **etchants** or **cleaners** in semiconductor manufacturing, removing metal oxide residues (e.g., copper oxide).
- Photoresist Additives:
Used to enhance the resolution of photolithography processes.
3. Nuclear Fuel & Radioactive Element Processing
- Extraction of Actinides:
HFA forms stable complexes with uranium (U), thorium (Th), and plutonium (Pu), aiding in **nuclear fuel recycling** and **radioactive waste treatment**.
4. Analytical Chemistry
- Derivatization Reagent:
Improves sensitivity and selectivity in **mass spectrometry (MS)** and **gas chromatography (GC)** by chelating metal ions (e.g., Al³⁺, Fe³⁺).
- Sensor Materials:
Used in fluorescent or electrochemical sensors for metal ion detection.
5. Catalysis & Ligands
- Organic Reaction Catalyst:
Acts as a **Lewis acid ligand** in oxidation, polymerization, or cyclization reactions (e.g., olefin epoxidation).
- Asymmetric Synthesis:
Chiral HFA derivatives enable **asymmetric catalysis**.
6. Other Applications
- Stabilizer:
Prevents thermal degradation in polymers.
- Pharmaceutical Intermediate:
Used in synthesizing **fluorinated drugs** or bioactive molecules.
Key Advantages
HFA’s **strong electron-withdrawing fluorine atoms** contribute to its high stability, volatility, and strong metal-coordinating ability, making it indispensable in advanced industrial and scientific research.
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