Nickel tetracarbonyl
Nickel tetracarbonyl, also known as tetracarbonylnickel, is a highly toxic organometallic compound with the formula Ni(CO)₄. It is a volatile, colorless liquid that is notable for its role in the Mond process for purifying nickel.
Structure and Properties
Nickel tetracarbonyl is a coordination complex of nickel with carbon monoxide. The molecule is tetrahedral, with the nickel atom at the center surrounded by four carbon monoxide ligands. This geometry is typical for a 16-electron complex, which is relatively rare and contributes to its high reactivity.
The compound is diamagnetic, indicating that all electrons are paired. The Ni–C bond distances are approximately 1.83 Å, and the C–O bond distances are about 1.15 Å, which are consistent with other metal carbonyls.
Synthesis
Nickel tetracarbonyl is synthesized by the direct reaction of nickel metal with carbon monoxide:
- Ni + 4 CO → Ni(CO)₄
This reaction is highly exothermic and occurs at room temperature under a carbon monoxide atmosphere. The process is reversible, and nickel tetracarbonyl can decompose back into nickel and carbon monoxide upon heating.
Applications
Nickel tetracarbonyl is primarily used in the Mond process for the purification of nickel. In this process, impure nickel is reacted with carbon monoxide to form nickel tetracarbonyl, which is then decomposed at higher temperatures to yield pure nickel metal.
Toxicity and Safety
Nickel tetracarbonyl is extremely toxic and poses significant health risks. It is a potent carcinogen and can cause severe respiratory damage upon inhalation. Exposure to nickel tetracarbonyl can lead to symptoms such as headache, dizziness, and nausea, and prolonged exposure can be fatal.
Due to its high volatility and toxicity, nickel tetracarbonyl must be handled with extreme care, using appropriate protective equipment and ventilation.
Related Compounds
Nickel tetracarbonyl is part of a broader class of compounds known as metal carbonyls, which are complexes of transition metals with carbon monoxide ligands. Other examples include iron pentacarbonyl and cobalt carbonyl.
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See Also
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Contributors: Prab R. Tumpati, MD