Self-assembling dicopper(II) complexes of di-2-pyridyl ketone Schiff base ligands derived from S-alkyldithiocarbazates

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• 作者：Mohammad Akbar Ali^a ; ^{palonkuri@yahoo.com"" rel=""nofollow} ; Aminul H. Mirza^a ; Ray J. Butcher^b ; Paul V. Bernhardt^c ; Mohammad Rezaul Karim^d
• 关键词：Di-2-pyridyl ketone Schiff base of S-benzyldithiocarbazate ; Copper(II) complexes ; Dithiocarbazates
• 刊名：Polyhedron
• 出版年：2011
• 出版时间：26 May 2011
• 年：2011
• 卷：30
• 期：9
• 页码：1478-1486
• 全文大小：935 K

文摘

Condensation of di-2-pyridyl ketone with S-methyldithiocarbazate or S-benzyldithiocarbazate yields potentially bridging ligands of the form Py₂CNNHC(S)SR; Hdpksme (R = Me; the di-2-pyridyl ketone Schiff base of S-methyldithiocarbazate) and Hdpksbz (R = Bz; the di-2-pyridyl ketone Schiff base of S-benzyldithiocarbazate). Complexation of these ligands with Cu(II) in a 1:1 M ratio leads to the formation of dinuclear complexes of the general formula [Cu(NNNS)X]₂ (X = Cl^−, NO₃^−, H₂O). X-ray crystallographic structure determinations show that each ligand provides three donor atoms (NNS) in a meridional configuration to one metal, viz. one of the pyridine nitrogen atoms, the azomethine nitrogen atom and the thiolate sulfur, while the nitrogen atom of the second pyridyl group forms a bridge to another copper(II) ion within the dimer. The coordination geometry around each copper(II) ion is approximately square pyramidal, the basal plane of which is composed of one of the pyridine nitrogen atoms, the azomethine nitrogen atom and a chlorido, nitrato or aqua ligand. The apical position of the square pyramid is always occupied by the pyridine nitrogen atom of the second ligand.