Nickel(II) bis(acetylacetonate)

From WikiMD's Food, Medicine & Wellness Encyclopedia

Nickel(II) bis(acetylacetonate) is a chemical compound with the formula Ni(C5H7O2)2. It is a coordination complex of nickel with acetylacetonate (acac), a negatively charged bidentate ligand formed by deprotonation of acetylacetone (2,4-pentanedione). This compound is of interest both in the field of coordination chemistry and for its applications in catalysis, particularly in processes involving olefin polymerization and alkene oxidation.

Structure and Properties[edit | edit source]

Nickel(II) bis(acetylacetonate) is characterized by a square planar geometry around the nickel center, typical for d8 metal ions such as nickel(II). The nickel atom is coordinated by two oxygen atoms from each acetylacetonate ligand. The ligands are arranged in a planar, chelating manner, which stabilizes the metal center and contributes to the compound's overall stability.

The compound is usually encountered as a green solid, which is soluble in organic solvents such as chloroform, ethanol, and diethyl ether. Its solubility in these solvents makes it useful in organic synthesis and catalytic processes that require a homogeneous catalyst.

Synthesis[edit | edit source]

Nickel(II) bis(acetylacetonate) can be synthesized by reacting nickel(II) salts, such as nickel(II) chloride, with acetylacetone in the presence of a base. The base, typically a tertiary amine like triethylamine, deprotonates the acetylacetone, forming the acac ligand, which then coordinates to the nickel ion. The reaction typically yields the nickel complex as a green precipitate:

NiCl2 + 2 C5H8O2 + 2 NEt3 → Ni(C5H7O2)2 + 2 NEt3HCl

Applications[edit | edit source]

Nickel(II) bis(acetylacetonate) serves as a versatile catalyst in organic synthesis. It is particularly effective in the polymerization of olefins, where it can act as a catalyst for both the oligomerization and polymerization of ethylene and other alkenes. Additionally, it has been employed in the oxidation of alkenes to ketones, an important reaction in the synthesis of fine chemicals and pharmaceutical intermediates.

Safety and Handling[edit | edit source]

As with many nickel compounds, nickel(II) bis(acetylacetonate) is considered to be potentially hazardous. It can cause allergic skin reactions and is suspected of causing cancer. Proper personal protective equipment, including gloves and eye protection, should be used when handling this compound. Additionally, operations involving this compound should be conducted in a well-ventilated area or under a fume hood to minimize exposure to dust or vapors.

See Also[edit | edit source]

References[edit | edit source]


Wiki.png

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD


Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD