Article ID Journal Published Year Pages File Type
1339769 Polyhedron 2007 11 Pages PDF
Abstract

The present work illustrates the versatile coordination modes of the amide-based ligands towards copper(II) ion. The reaction of the deprotonated form of the ligand, [L1]2− with CuCl2 affords a linear trinuclear complex, [Cu3(L1)2(Cl)2(H2O)] (1) which has been characterized thoroughly including single crystal structure analysis. The structure of 1 shows that one of the arm of the flexible ligand flips to coordinate second copper(II) centre, resulting in the formation of a trinuclear complex. On the other hand, ligand H2L2 in its deprotonated form reacts with Cu(II) ion to give complex 2 with general formula, [Cu(L2)]n (2). The crystal structure of the complex 2 shows that each copper is square-pyramidal with 5th coordination coming from the O-atom of the amide group from a neighbouring complex. This results in the generation of an one-dimensional zig-zag chain. The variable temperature magnetic measurements of the complexes, 1 and 2 show that while Cu ions in the former are antiferromagnetically coupled (J = −110.34 cm−1), a weak ferromagnetic interaction (J = +3.08 cm−1) exists in the later. A rationale, based on the orbital overlap from the copper ions and associated ligands, is provided for the observed magnetic coupling between the copper ions.

Graphical abstractNovel copper(II) complexes of amide-based ligands are reported having linear trimeric (1) and one-dimensional zig-zag chain (2) structures. The copper centers bridged by the amidic NCO group (highlighted in pink shade) show interesting but contrast magnetic properties. The complex 1 shows antiferromagnetic coupling (J = −110 cm−1) while 2 shows a weak ferromagnetic interaction (J = +3 cm−1).Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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