Syntheses, crystal structures, spectroscopic, fluorescence and thermal properties of silver(I) 5,5-diethylbarbiturato complexes with some aminopyridines

YILMAZ F., YILMAZ V. T., Soyer E., Buyukgungor O.

INORGANICA CHIMICA ACTA, vol.363, no.13, pp.3165-3171, 2010 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 363 Issue: 13
  • Publication Date: 2010
  • Doi Number: 10.1016/j.ica.2010.05.050
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.3165-3171
  • Keywords: 5,5-Diethylbarbiturate, Silver(I), 2-Aminopyridine, 2-Aminomethylpyridine, 2-(Dimethylaminomethyl)-3-hydroxypyridine, ANTIMICROBIAL ACTIVITY, COPPER(II), LIGANDS, 2-(2-AMINOETHYL)PYRIDINE, ZINC
  • Ondokuz Mayıs University Affiliated: Yes


Three new silver(I) complexes of 5,5-diethlybarbiturate (barb), [Ag(mu-barb)(apy)]center dot H(2)O (1), {[Ag(mu-lampy)][Ag(mu-barb)2]}n (2) and [Ag(barb)(dmamhpy)] (3) [apy = 2-aminopyridine, ampy = 2-aminomethylpyridine and dmamhpy = 2-(dimethylaminomethyl)-3-hydroxypyridine] have been synthesized and characterized by elemental analysis and FT-IR. Single crystal X-ray diffraction analyses showed that complexes 1 and 3 are mononuclear. In 1, the silver(I) ion is linearly coordinated by a barb anion and a ampy ligand, while a bidentate dmamhpy ligand together with an N-coordinated barb anion forms a trigonal coordination geometry around silver(I) in 3. Complex 2 is a one-dimensional coordination polymer in which silver(I) ions are bridged by ampy ligands, leading to a cationic chain [Agd(ampy)](+)(n). The [Ag(barb)(2)] units contains two N-bonded barb ligands, bridging the silver centers in the cationic and anionic units via the carbonyl O atoms. Thus, complex 2 contains two-coordinated and four-coordinated silver ions. All complexes display hydrogen-bonded network structures and exhibit appreciable fluorescence at room temperature. Thermal analysis (TG-DTA) data are in agreement with the structures of the complexes. (C) 2010 Elsevier B.V. All rights reserved.