Triphenylmethyl radical

Triphenylmethyl radical
Kekulé, skeletal formula of the triphenylmethyl radical
Kekulé, skeletal formula of the triphenylmethyl radical
Ball-and-stick model of the triphenylmethyl radical
Names
Preferred IUPAC name
Triphenylmethyl
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C19H15/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H checkY
    Key: OHSJPLSEQNCRLW-UHFFFAOYSA-N checkY
  • c1ccc(cc1)[C](c1ccccc1)c1ccccc1
  • C1=CC=C(C=C1)[C](C1=CC=CC=C1)C1=CC=CC=C1
Properties
C19H15
Molar mass 243.329 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkYX markN ?)
Infobox references

The triphenylmethyl radical (often shortened to trityl radical after 1927 suggestion by Helferich et al.[1]) is an organic compound with the formula (C6H5)3C. It is a persistent radical. It was the first radical to be described in organic chemistry. Because of its accessibility, the trityl radical has been heavily investigated.[2]

Preparation and properties

The triphenylmethyl radical can be prepared by reduction of triphenylmethyl chloride. A variety of reductants can be employed including silver.

(C6H5)3CCl + Ag → (C6H5)3C· + AgCl

The trityl radical exists in a chemical equilibrium with the quinoid-type dimer, called Gomberg's dimer. In benzene the concentration of the radical is 2%.[3]

Triphenylmethyl radical
Triphenylmethyl radical

Solutions containing the radical are yellow; when the temperature of the solution is raised, the yellow color becomes more intense as the equilibrium is shifted in favor of the radical rather than the colorless dimer, in accordance with Le Chatelier's principle.

The triphenylmethyl radical exhibits green photoluminescence. Further reaction of the quinoid dimer with another triphenylmethyl radical produces a quinoid radical that exhibits red photoluminescence.[4]

When exposed to air, the radical rapidly oxidizes to the peroxide, and the color of the solution changes from yellow to colorless. Likewise, the radical reacts with iodine to triphenylmethyl iodide.

Triphenylmethyl radical oxidation
Triphenylmethyl radical oxidation

Trityl derivatives

Whereas the triphenyl radical forms a quinoid dimer, substitution at the para ring positions completely inhibits dimer formation entirely.[5] Other derivatives of the triphenyl radical with certain substituted phenyl groups do form dimers with a hexaphenylethane-like structure. For example, the tris(3,5-di-tert-butylphenyl) radical dimerizes to give hexakis(3,5-di-t-butylphenyl)ethane, with a bond length of 1.67 Å for the central carbon–carbon bond. Theoretical calculations on a very high level of theory indicate that van der Waals attraction between the tert-butyl groups create a potential minimum that is absent in the unsubstituted molecule.[6][7] Other derivatives have been reported as the quinoid dimer [8]


History

The radical was discovered by Moses Gomberg in 1900 at the University of Michigan.[9][10][11] He tried to prepare hexaphenylethane from triphenylmethyl chloride 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 discovered structure was used in the development of ESR spectroscopy and confirmed by it.[12][13][14] The triphenylmethyl radical, and the larger class of triarylmethyl radicals, are called Gomberg radicals.[4][15]

The quinoid structure for the dimer was suggested as early as 1904 but this structure was soon after abandoned in favor of hexaphenylethane (4).[16] It subsequently took until 1968 for its rediscovery when researchers at the Vrije Universiteit Amsterdam published proton NMR data.[17]

Further reading

  • Shishlov, Nikolay M. (2006). "From the Gomberg radical to organic magnets". Russian Chemical Reviews. 75 (10): 863–884. doi:10.1070/RC2006v075n10ABEH003621.

See also

References

  1. ↑ Helferich, B.; Bredereck, H.; Schneidmüller, A. (1927). "Acylwanderung an partiell acylierten Methyl-glucosiden". Justus Liebigs Annalen der Chemie (in German). 458 (1): 111–116. doi:10.1002/jlac.19274580108. ISSN 0075-4617.
  2. ↑ Tidwell, Thomas T. (2010). "Triarylmethyl and Related Radicals". Stable Radicals. pp. 1–31. doi:10.1002/9780470666975.ch1. ISBN 9780470666975.
  3. ↑ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 271, ISBN 978-0-471-72091-1
  4. 1 2 Bulgakov, Ramil G.; Kuleshov, Sergei P.; Valiullina, Zemfira S. (2000). "Red photoluminescence in the synthesis of triphenylmethyl radicals by the Gomberg method". Mendeleev Communications. 10: 22–23. doi:10.1070/MC2000v010n01ABEH001115.
  5. ↑ Dünnebacke, Dieter; Neumann, Wilhelm P.; Penenory, Alicia; Stewen, Ulrich (1989). "Über sterisch gehinderte freie Radikale, XIX. Stabile 4,4′,4″-trisubstituierte Triphenylmethyl-Radikale". Chemische Berichte. 122 (3): 533–535. doi:10.1002/cber.19891220322.
  6. ↑ Lewars, Errol (2008), "8. Hexaphenylethane", Modeling Marvels, Springer, Bibcode:2008moma.book.....L
  7. ↑ Grimme, Stefan; Schreiner, Peter R. (2011). "Steric crowding can stabilize a labile molecule: Solving the hexaphenylethane riddle". Angewandte Chemie International Edition. 50 (52): 12639–12642. doi:10.1002/anie.201103615. PMID 22025456.
  8. ↑ Uchimura, Y.; Takeda, T.; Katoono, R.; Fujiwara, K.; Suzuki, T. (2015). "New Insights into the Hexaphenylethane Riddle: Formation of an α,o-Dimer". Angewandte Chemie International Edition. 54 (13): 4010–4013. doi:10.1002/anie.201500122. PMID 25704856.
  9. ↑ Gomberg, M. (1900). "An instance of trivalent carbon: triphenylmethyl". Journal of the American Chemical Society. 22 (11): 757–771. doi:10.1021/ja02049a006.
  10. ↑ Gomberg, M. (1901). "On trivalent carbon". Journal of the American Chemical Society. 23 (7): 496–502. doi:10.1021/ja02033a015. (Note: radical is also called a cadicle.)
  11. ↑ Gomberg, M. (1902). "On trivalent carbon". Journal of the American Chemical Society. 24 (7): 597–628. doi:10.1021/ja02021a001.
  12. ↑ Weissman, S. I.; Sowden, John C. (1953). "Electron distribution in triphenylmethyl: Hyperfine structure of the paramagnetic resonance absorption of (C6H5)3C13*". Journal of the American Chemical Society. 75 (2): 503. doi:10.1021/ja01098a522.
  13. ↑ Sinclair, J.; Kivelson, D. (1968). "Electron spin resonance studies of substituted triphenylmethyl radicals". Journal of the American Chemical Society. 90 (19): 5074–5080. doi:10.1021/ja01021a004.
  14. ↑ "ESR spectrum of the triphenylmethyl radical". School of Chemistry, University of Bristol. Retrieved August 5, 2018.
  15. ↑ Shishlov, Nikolay M. (2006). "From the Gomberg radical to organic magnets". Russian Chemical Reviews. 75 (10): 863–884. doi:10.1070/RC2006v075n10ABEH003621.
  16. ↑ McBride, J. M. (1974). "The hexaphenylethane riddle". Tetrahedron. 30 (14): 2009–2022. doi:10.1016/S0040-4020(01)97332-6.
  17. ↑ Lankamp, H.; Nauta, W. Th.; MacLean, C. (1968). "A new interpretation of the monomer–dimer equilibrium of triphenylmethyl- and alkyl-substituted-diphenyl methyl-radicals in solution". Tetrahedron Letters. 9 (2): 249–254. doi:10.1016/S0040-4039(00)75598-5.
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