کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1338556 | 979671 | 2011 | 6 صفحه PDF | دانلود رایگان |

Synthesis and single crystal X-ray diffraction studies of four transition metal complexes [Mn(L1)](ClO4)2 (1), [Cu(L1)](ClO4)2 (2), [Ni2(L2)(NCS)6][Ni(L1)] (3) and [Mn(bzpy)(NCS)2] (4) with neutral ligands [L1 = N-(1-pyridin-2-yl-phenylidene)-N′-[2-({2-[(1-pyridin-2-yl phenylidene)amino]ethyl}amino)ethyl]ethane-1,2diamine, L2 = N-(1-pyridin-2-yl-phenylidene)-N′-[2-({2-[(1-pyridin-2-ylphenylidene)amino]ethyl}piperazine-1yl)ethyl]amine, bzpy = 2-benzoylpyridine] are reported. The trinuclear nickel(II) complex 3 is made of a dinuclear anion and a mononuclear cation. Variable-temperature magnetic susceptibility and variable-field magnetisation studies performed on 3 suggest weak antiferromagnetic coupling (J = −0.7 cm−1) between the two metals of the dinuclear entity, but no magnetic interaction between the anionic and cationic counterparts.
Synthesis and single crystal X-ray diffraction studies of four transition metal complexes [Mn(L1)](ClO4)2 (1), [Cu(L1)](ClO4)2 (2), [Ni2(L2)(NCS)6][Ni(L1)] (3) and [Mn(bzpy)(NCS)2] (4) with neutral ligands [L1 = N-(1-pyridin-2-yl-phenylidene)-N′-[2-({2-[(1-pyridin-2-yl phenylidene)amino]ethyl}amino)ethyl]ethane-1,2diamine, L2 = N-(1-pyridin-2-yl-phenylidene)-N′-[2-({2-[(1-pyridin-2-ylphenylidene)amino]ethyl}piperazine-1yl)ethyl]amine, bzpy = 2-benzoylpyridine] are reported. The trinuclear nickel(II) complex 3 is made of a dinuclear anion and a mononuclear cation. Variable-temperature magnetic susceptibility and variable-field magnetization studies performed on 3 suggest weak antiferromagnetic coupling (J = −0.7 cm−1) between the two metals of the dinuclear entity, but no magnetic interaction between the anionic and cationic counterparts.Figure optionsDownload as PowerPoint slideHighlights
► Synthetic coordination chemistry.
► Chemistry of Schiff bases as ligands.
► Molecular magnetism.
Journal: Polyhedron - Volume 30, Issue 12, 2 August 2011, Pages 2032–2037