Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/23876
Title: Syntheses, crystal structures, fluorescent, and thermal properties of nickel(II) 5,5-diethylbarbiturate complexes with (2-aminomethyl), (2-aminoethyl), and (2-hydroxyethyl)pyridines
Authors: Yılmaz, Fatih
Büyükgüngör, Orhan
Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.
0000-0002-2849-3332
Yılmaz, Veysel Turan
Güney, Emel
L-7238-2018
7006269202
25027291500
Keywords: Chemistry
5
5-Diethylbarbiturate
(2-Aminomethyl)pyridine(2-Aminoethyl)pyridine
(2-Hydroxyethyl)pyridine
Nickel(II)
Copper(II)
Acid
Issue Date: 2011
Publisher: Taylor & Francis
Citation: Yılmaz, V. T. vd. (2011). ''Syntheses, crystal structures, fluorescent, and thermal properties of nickel(II) 5,5-diethylbarbiturate complexes with (2-aminomethyl), (2-aminoethyl), and (2-hydroxyethyl)pyridines''. Journal of Coordination Chemistry, 64(1), Special Issue, 159-169.
Abstract: Three nickel(II) complexes of 5,5-diethlybarbiturate (barb) with (2-aminomethyl)pyridine (ampy), (2-aminoethyl)pyridine (aepy), and (2-hydroxyethyl)pyridine (hepy), [Ni(barb-N)2(ampy)2] (1), [Ni(barb-N,O)(aepy)2](barb) center dot H2O (2), and [Ni(barb-O)2(hepy)] center dot 2H2O (3), have been synthesized and characterized by elemental analysis, IR, thermal analysis, and single crystal X-ray diffraction. All complexes are mononuclear with nickel(II) exhibiting an octahedral coordination. Ampy, aepy, and hepy are bidentate chelating ligands, while barb shows different coordination modes. In 1, two barb ligands are N-bonded, whereas in 3 they are O-coordinated through one carbonyl oxygen. In 2, one barb is bidentate chelating, while the second barb remains outside the coordination sphere as a counterion. The molecules of 1-3 are bridged by multiple hydrogen bonds to generate 1-D or 2-D supramolecular networks. All complexes are fluorescent due to -* transitions.
URI: https://doi.org/10.1080/00958972.2010.537333
https://www.tandfonline.com/doi/full/10.1080/00958972.2010.537333
http://hdl.handle.net/11452/23876
ISSN: 0095-8972
Appears in Collections:Scopus
Web of Science

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