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The triphenylmethyl radical is a persistent radical and the first ever radical described in organic chemistry. It can be prepared by homolysis of triphenylmethylchloride 1 (scheme 1) by a metal like silver or zinc in benzene or diethyl ether. The radical 2 forms a chemical equilibrium with the quinoid type dimer 3. In benzene the concentration of the radical is 2% .
Additional recommended knowledge
Solutions containing the radical are yellow and when the temperature of the solution is increased the yellow color becomes more intense as the equilibrium is shifted in favor of the radical following Le Chatelier's principle. Conversely when the solution is cooled it becomes less yellow.
When exposed to air the radical rapidly oxidizes to the peroxide (Scheme 2) and the color of the solution changes from yellow to colorless. Likewise, the radical reacts with iodine to triphenylmethyliodide.
The radical was discovered by Moses Gomberg in 1900. He tried to prepare hexaphenylethane from triphenylmethylchloride and zinc in benzene in a Wurtz reaction and found that the product, based on its behaviour towards iodine and oxygen, was far more reactive than anticipated.
The correct quinoid structure for the dimer was suggested as early as 1904 but this structure was soon after abandoned by the scientific community in favor of hexaphenylethane which is structure 4 in scheme 1 . It subsequently took until 1968 for its rediscovery when researchers at the Vrije Universiteit Amsterdam published proton NMR data . In hindsight the substituted ethane molecule does not make sense at all because it is simply too sterically overcrowded.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Triphenylmethyl_radical". A list of authors is available in Wikipedia.|