Titrations in non-aqueous media part xv.* redoximetric titrations of anthracene and anthracene derivatives with manganese(III) acetate in glacial acetic acid


Gündüz T., Kiliç E., Güi Öztaş S. G.

The Analyst, cilt.114, sa.2, ss.225-226, 1989 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 114 Sayı: 2
  • Basım Tarihi: 1989
  • Doi Numarası: 10.1039/an9891400225
  • Dergi Adı: The Analyst
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.225-226
  • Anahtar Kelimeler: Manganese(iii) acetate, Non-aqueous media, Redoximetric titrations, Titrations of anthracene and its derivatives
  • Ankara Üniversitesi Adresli: Evet

Özet

Anthracene, 9-methylanthracene, 9-phenylanthracene, 9-chloroanthracene, 9-anthracenecarbaldehyde, 9,10-diphenylanthracene, 9,10-dibromoanthracene, 9,10-anthracenedicarbaldehyde, 9,10-ditolylanthracene, 9-cyanoanthracene, 9,10-dicyanoanthracene, 9-cyano-10-methoxyanthracene, 9-chloro-10- cyanoanthracene and dibenz[a,h]anthracene were titrated redoximetrically with manganese(III) acetate in glacial acetic acid. Titrations were carried out at 60 °C, both directly and indirectly. Because the direct titrations are time consuming, the indirect titrations were found to be the more practical. For the indirect titrations a hydroquinone solution was used as a back-titrant. The end-points were determined potentiometrically using a redox platinum and silver - silver chloride electrode assembly. The first nine compounds listed above participated in two-electron redox reactions to produce anthraquinone and its derivatives. The remaining five compounds did not undergo a redox reaction. This is probably due to the very strong electron-withdrawing effect of the cyano group or to the fused benzene rings.