4.5 Article

One Ferromagnetic and Two Antiferromagnetic Dinuclear Nickel(II) Complexes Derived from a Tridentate N,N,O-Donor Schiff Base Ligand: A Density Functional Study of Magnetic Coupling

期刊

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 -, 期 17, 页码 2916-2927

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201200028

关键词

Nickel; Schiff bases; O ligands; Magnetic properties; Density functional calculations

资金

  1. Council of Scientific and Industrial Research (CSIR)
  2. Government of India [09/028(0746)/2009-EMR-I, 09/080(0639)/2009-EMR-I]
  3. Department of Science Technology
  4. DST - Centre for Nanotechnology, Indian Association for the Cultivation of Science (IACS)

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Three new dinuclear NiII complexes, [Ni2L2(NO3)2] (1), [Ni2L2(NO2)2] (2), and [Ni2L2(CH3COO)2(H2O)] (3), have been synthesized by using a tridentate Schiff base ligand, 2-({[3-(dimethylamino)propyl]imino}methyl)phenol (HL), along with a nitrate, nitrite, or acetate ion, respectively, as co-ligand. These three complexes were characterized by spectral analysis, X-ray crystallography, and variable-temperature magnetic susceptibility measurements. The structural analyses revealed that the NiII ions are coordinated by the deprotonated chelating tridentate Schiff base and possess a distorted octahedral geometry in all three complexes. Complexes 1 and 2 are two di-mu 2-phenoxido-bridged species in which the nitrate and nitrite act as chelating co-ligands. However, in complex 3, in which the acetate anion is monodentate, an additional water bridge is present along with two mu 2-phenoxido bridges making the complex a face-sharing bi-octahedron. Magnetic susceptibility measurements indicate an antiferromagnetic intradimer interaction in complexes 1 and 2 with J values of 20.34(5) and 25.25(4) cm1, respectively, whereas complex 3 shows a dominant ferromagnetic exchange coupling with J = 19.11(9) cm1. DFT calculations were performed, and the theoretically obtained J values of 19.99 (for 1), 24.19 (for 2) and 18.81 cm1 (for 3) corroborate very well the experimental results. An attempt has also been made to correlate the effect of Ni center dot Ni distances and bridging NiONi angles on the coupling constants of the NiII complexes through DFT calculations. The relative energy calculations show that the diphenoxido-bridged complexes are stable at larger bridging angles, and consequently the coupling is antiferromagnetic, whereas with an additional water bridge, the formation of complexes with the NiONi bridging angle in the ferromagnetic region is energetically profitable.

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