On the complex forming tendencies of phenolic hydroxyls with scandium(III)

Turkel N., Guney E., Ozer U.

REVIEWS IN INORGANIC CHEMISTRY, cilt.26, sa.5, ss.493-506, 2006 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 26 Sayı: 5
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1515/revic.2006.26.5.493
  • Dergi Adı: REVIEWS IN INORGANIC CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.493-506
  • Bursa Uludağ Üniversitesi Adresli: Hayır

Özet

The complex forming tendencies of some diphenols: 1,8-dihydroxynaphthalene-3,6-disulphonate (chromotropic acid: CTA: (H2L)(2-)] and 3,4-dihydroxybenzaldehyde (3,4-DHBAL: H2L) with scandium(III) were investigated in aqueous solution by potentiometry and spectroscopy. The measurements were carried out at 25.0 +/- 0.1 degrees C and at an ionic strength of 0.1mol.dm(-3) KCl. The stochiometric protonation constants of 3,4-DHBAL, CTA and the stochiometric formation constants of their Sc3+ ((aq)) complex species were determined. (ScL)(-) type binary complex of CTA is stronger than (ScL)(-) type binary complex of 3,4-DHBAL. The hydrolysis of CTA complexes resulted in [ScL(OH)](2-) and [ScL(OH)(2)](3-) type mixed hydroxo complexes, whereas Sc3+-3,4-DHBAL complex hydrolysis also occurs and the existence of only [ScL(OH)(2)](-) type is complex verified. Sc3+ ((aq)) can achieve coordination number seven in CTA complex while it is six in 3,4-DHBAL complex.