- Source: Sodium naphthalene
Sodium naphthalene is an organic salt with the chemical formula Na+[C10H8]−. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na+.
Preparation and properties
The alkali metal naphthalene salts are prepared by stirring the metal with naphthalene in an ethereal solvent, usually as tetrahydrofuran or dimethoxyethane. The resulting salt is dark green. The anion is a radical, giving a strong EPR signal near g = 2.0. Its deep green color arises from absorptions centered at 463 and 735 nm.
Several solvates of sodium naphthalenide have been characterized by X-ray crystallography. The effects are subtle, the outer pair of CH−CH bonds contract by 3 pm and the other nine C−C bonds elongate by 2–3 pm. The net effect is that reduction weakens the bonding.
Reactions
= Redox
=With a reduction potential near −2.5 V vs NHE, the naphthalene radical anion is a strong reducing agent. It is capable of defluorinating PTFE and is commonly used for chemically etching PTFE to allow adhesion.
= Protonation
=The anion is strongly basic, and a typical degradation pathway involves reaction with water and related protic sources such as alcohols. These reactions afford dihydronaphthalene:
2 Na+[C10H8]− + 2 H2O → C10H10 + C10H8 + 2 NaOH
= As a ligand
=Alkali metal salts of the naphthalene radical anion are used to prepare complexes of naphthalene.
Related reagents
References
Kata Kunci Pencarian:
- Boron
- Kamus rumus kimia
- Sodium naphthalene
- Naphthalene
- Surface treatment of PTFE
- Radical anion
- Sodium
- Sodium chloride
- Lithium naphthalene
- 1-Methylnaphthalene
- Sodium compounds
- Sodium hydroxide
