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Triangular Ni2Ln and Ni2Y complexes derived from di-2-pyridyl ketone: Synthesis, structures and magnetic properties |
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| Authors: | Anastasia N GeorgopoulouConstantinos G Efthymiou Constantina PapatriantafyllopoulouVassilis Psycharis Catherine P RaptopoulouManolis Manos Anastasios J TasiopoulosAlbert Escuer Spyros P Perlepes |
| Institution: | a Institute of Materials Science, NCSR ‘Demokritos’, 153 10 Aghia Paraskevi Attikis, Greece b Department of Chemistry, University of Patras, 265 04 Patras, Greece c Department of Chemistry, University of Cyprus, 1678 Nicosia, Cyprus d Departament de Quimica Inorganica, Universitat de Barcelona, Marti Franques 1-11, Barcelona 08028, Spain |
| Abstract: | The synthetic investigation of the NiII/M(NO3)3·6H2O/di-2-pyridyl ketone (py)2CO] tertiary reaction system in EtOH has yielded triangular Ni2M cationic complexes (M = lanthanide, Y). The reaction between Ln(NO3)3·6H2O, Ni(ClO4)2·6H2O, (py)2CO and base (1:3:3:3) in EtOH under gentle heating gave the isostructural complexes Ni2Ln{(py)2C(OEt)(O)}3{(py)2C(OH)(O)}(NO3)(H2O)](ClO4)2 (Ln = Gd, 2; Ln = Tb, 3) in high yields. The ligands (py)2C(OEt)(O)− and (py)2C(OH)(O)− are the monoanions of the hemiketal and gem-diol derivatives of (py)2CO, respectively, formed in situ in the presence of the metal ions. The cations of 2 and 3 consist of one 8-coordinate LnIII and two distorted octahedral NiII atoms in an essentially isosceles, triangular arrangement capped by a central μ3-Ο− atom of the unique 3.3011 (Harris notation) (py)2C(OH)(O)− ligand. Each metal-metal edge is bridged by the deprotonated O atom of one 2.2011 (py)2C(OEt)(O)− ligand. The isostructural complexes Ni2M{(py)2C(OEt)(O)}4(NO3)(H2O)]2M(NO3)5](ClO4)2 (M = Y, 4 ; M = Tb, 5 ; M = Dy, 6) were prepared by the 1:1 reaction of the mononuclear “metalloligand” Ni(O2CMe){(py)2CO}{(py)2C(OH)2}](ClO4) (1) and M(NO3)3·6H2O in EtOH under mild heating in moderate to good yields. The structures of the dications of 4-6 are similar to those in 2 and 3, the only difference being the replacement of the unique 3.3011 (py)2C(OH)(O)− ligand of the latter by one 3.3011 (py)2C(OEt)(O)− group in the former. The YIII, TbIII and DyIII atoms in M(NO3)5]2− are coordinated by five bidentate chelating nitrato groups. Characteristic IR bands of the complexes are discussed in terms of the known structures and the coordination modes of the ligands. Variable temperature, solid-state direct current magnetic susceptibility and magnetization studies were carried out on dried samples of 2-4. The data indicate ferromagnetic Ni?Ni and Ni?Gd exchange interactions, and an ST = 11/2 ground state for 2. Complex 3 is characterized by a high-spin ground state while the ferromagnetic Ni?Ni interaction for 2 is independently supported by the study of 4. No out-of-phase, alternating current susceptibility signals have been detected for 3 that would be indicative of SMM behavior. |
| Keywords: | Crystal structures Di-2-pyridyl ketone-based ligands Heterometallic complexes Magnetic properties Nickel(II)/lanthanide(III) complexes Nickel(II)/yttrium(III) complexes |
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