2,2',2''-terpyridine
Sign in to saveAlso known as [2,2';6',2'']Terpyridine, alpha,alpha',alpha''-Terpyridine, alpha,alpha',alpha''-Tripyridyl, 2,2',2''-Tripyridine, 2,2',2''-Tripyridyl, 2,2',2''-Terpyridyl, Tripyridyl, Tripyridine
Terpyridine (2,2';6',2"-terpyridine, often abbreviated to Terpy or Tpy) is a heterocyclic compound derived from pyridine. It is a white solid that is soluble in most organic solvents. The compound is mainly used as a ligand in coordination chemistry.
Wikidata facts
- Mass
- 233.095
Show 3 more facts
- chemical formula
- C₁₅H₁₁N₃
- canonical SMILES
- C1=CC=NC(=C1)C2=NC(=CC=C2)C3=CC=CC=N3
- melting point
- 91.0
via Wikidata · CC0
~3 min read
Encyclopedic overview
5 sectionsContents
- Synthesis
- Properties
- Related compounds
- See also
- References
Terpyridine (2,2';6',2"-terpyridine, often abbreviated to Terpy or Tpy) is a heterocyclic compound derived from pyridine. It is a white solid that is soluble in most organic solvents. The compound is mainly used as a ligand in coordination chemistry.
==Synthesis== Terpyridine was first synthesized by G. Morgan and F. H. Burstall in 1932 by the oxidative coupling of pyridines. This method, however, proceeded in low yields. More efficient syntheses have since been described, mainly starting from 2-acetylpyridine. One method produces an enaminone by the reaction of 2-acetylpyridine with N,N-dimethylformamide dimethyl acetal. The base-catalyzed reaction of 2-acetylpyridine with carbon disulfide followed by alkylation with methyl iodide gives C5H4NCOCH=C(SMe)2. Condensation of this species with 2-acetylpyridine forms the related 1,5-diketone, which condenses with ammonium acetate to form a terpyridine. Treatment of this derivative with Raney nickel removes the thioether group.
Excerpted from Wikipedia’s “2,2',2''-terpyridine” article, available under the CC BY-SA 4.0 licence.