Synthesis, crystal structure, spectroscopic, thermal, catechol oxidase and catalase-like studies: New copper(II) complexes of 2-benzoylbenzoate and 2-pyridilpropanol ligands


Çağlar S., Adiguzel E., Çağlar B., Saykal T., Şahin E., Buyukgungor O.

Inorganica Chimica Acta, cilt.397, ss.101-109, 2013 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 397
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1016/j.ica.2012.11.028
  • Dergi Adı: Inorganica Chimica Acta
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.101-109
  • Anahtar Kelimeler: 2-Benzoylbenzoic acid, Catalase activity, Catechol oxidation, Crystal structure, Dinuclear copper(II) complex
  • Erzincan Binali Yıldırım Üniversitesi Adresli: Evet

Özet

Two novel copper(II) complexes, mononuclear [Cu(bba)2(pypr) 2] 1 and dinuclear [Cu2(bba)2(pypr) 2] 2, have been synthesized by reactions of 2-pyridilpropanol with CuSO4·5H2O or Cu(CH3COO) 2·2H2O metal salt in the presence of 2-benzoylbenzoic acid. The copper(II) ion has a distorted octahedral geometry in 1 and distorted square pyramidal geometry in 2. 1 crystallizes in space group P1̄, while 2 crystallizes in the monoclinic crystal system with the space group P21/n. 2-Benzoylbenzoate behaves as a monodentate in 1, bidentate in 2. 2-pyridilpropanol ligand acts as a bidentate in 1 and bridging in 2. Both complexes were characterized by elemental analysis, mass and IR spectroscopy. Their molecular structures were determined by X-ray crystal structure analysis and their thermal stabilities were confirmed by TG/DTA/DTG techniques. Dinuclear compound shows high catalytic activity regarding the oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butylquinone exhibiting saturation kinetics at high substrate concentrations. In addition, dinuclear compound demonstrates significantly catalase-like activity. But mononuclear complex shows neither catalase-like nor catechol oxidase activity.© 2012 Elsevier B.V. All rights reserved.