A quinonoid zwitterion is a mesoionic zwitterion based on quinone-related chemical compounds. The benzene derivate 1,3-dihydroxy-4,6-diaminobenzene is easily oxidized by air in water or methanol to the quinonoid. This compound was first prepared in 1883 and the quinonoid structure first proposed in 1956. In 2002 the compound was found to be more stable and to exist as the zwitterion after a proton transfer.[1] Evidence for this structure is based on nuclear magnetic resonance spectroscopy and x-ray crystallography. The positive charge is delocalized between the amino groups over four bonds involving six pi electrons. The negative charge is spread likewise between the oxygen atoms.[2]

See also

  • Questiomycin A - an antibiotic compound containing the quinonoid group

References

  1. ↑ Siri, Olivier; Braunstein, Pierre (30 January 2002). "Unprecedented zwitterion in quinonoid chemistry". Chemical Communications (3): 208–209. doi:10.1039/B107828N.
  2. ↑ Haas, Yehuda; Zilberg, Shmuel (1 July 2004). "Charge Separation in Ground-State 1,2,4,5-Tetra-Substituted Benzene Derivatives". Journal of the American Chemical Society. 126 (29): 8991–8998. doi:10.1021/ja048872e.
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