A new unique tetranuclear Cu(II) compound with double bridging thiocyanate anions: Synthesis, X-ray structure and magnetism of [Cu 4(μ 1,3-NCS) 6(dpyam) 4(O 2CH) 2(H 2O) 2] (dpyam = di-2-pyridylamine)

Abstract

A new unique tetranuclear copper(II) complex doubly-bridged by thiocyanate anions [Cu 4(μ 1,3-NCS) 6(dpyam) 4(O 2CH) 2(H 2O) 2 (dpyam = di-2-pyridylamine) has been synthesized and characterized by X-ray diffraction methods and magnetic measurements. The “outer” Cu ions, with a CuN 3O(S, O) chromophore, have an axially elongated octahedral geometry. The basal plane of these outer Cu(II) ions consist of 2 nitrogen atoms of the dpyam ligand with Cu–N distances of 1.980(2) and 2.008(2) Å, one nitrogen atom of a bridging thiocyanate anion (Cu–N distance 1.961(3) Å) and an oxygen atom of a formate molecule (Cu–O distance 1.977(1) Å). The axial positions are occupied by an oxygen atom of a water molecule (Cu–O distance 2.518(1) Å and by a sulfur atom of a bridging thiocyanate anion at a semi-coordination distance of 3.048(1) Å. The “inner” Cu atoms, with a CuN 4(S 2) chromophore do also have an axially elongated octahedral geometry. The basal plane is formed by 2 nitrogen atoms of the dpyam ligand with Cu–N distances of 1.995(2) and 2.018(3) Å and two nitrogen atoms of two bridging thiocyanate anions (Cu–N distances 1.946(3), 1.976(3) Å). The axial positions are occupied by two sulfur atoms of two bridging thiocynate anions (Cu–S semi-coordinating distances are 2.875(1) and3.126(1) Å). Each Cu ion is bridged by two μ 1,3-NCS anions (in an equatorial-axial bridging mode) forming in this way a zigzag tetranuclear unit. The magnetic susceptibility data of the compound have been investigated between 5 and 200 K. The compound shows a very weak antiferromagnetic interaction between the Cu ions, in agreement with the non-overlapping magnetic orbitals of each Cu ion.