6533b86cfe1ef96bd12c8116
RESEARCH PRODUCT
Asymmetric bis-(μ1,1-azido) bridged dinuclear copper(II) complex with N2O donor Schiff base: synthesis, structure and magnetic study
Shouvik ChattopadhyayBikash Kumar ShawShyamal K. SahaMithun DasBiswa Nath GhoshKari Rissanensubject
Schiff baseStereochemistryDimerchemistry.chemical_elementschiff baseCopperchemistry.chemical_compoundCrystallographyMagnetizationCopper(II)Deprotonationchemistryfield-dependent magnetization studyantiferromagneticMaterials ChemistryMoleculeAntiferromagnetismAzidePhysical and Theoretical Chemistrydinuclearta116description
A copper(II) complex, [Cu2(L)2(N3)2] [where HL = 2-((3-(methylamino)propylimino)methyl)-6-methoxyphenol] has been synthesized and characterized by elemental analysis, IR, UV–vis and fluorescence spectroscopy, and single-crystal X-ray diffraction studies. The complex crystallizes in the trigonal space group R. The deprotonated tridentate Schiff base occupies three coordination sites of copper(II). The fourth coordination site is occupied by an azide. A symmetry-related azide from a different molecule coordinates with the fifth site of copper(II), thereby forming a double end-on azide-bridged centrosymmetric dimer. Variable temperature solid–state magnetic studies between 2 and 300 K were carried out and the data indicate predominant antiferromagnetic exchange interactions with 2J = –0.45 cm−1. The magnetic field-dependent magnetization study (M − H) reveals existence of antiferromagnetic ordering at a lower temperature (2 K) with a very small coercive field (~20 Oe) suggesting soft magnet behavior of the c...
year | journal | country | edition | language |
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2015-03-20 | Journal of Coordination Chemistry |