A new unique tetranuclear Cu(II) compound with double bridging thiocyanate anions: Synthesis, X-ray structure and magnetism of [Cu4(μ1,3-NCS)6(dpyam)4(O2CH)2(H2O)2] (dpyam = di-2-pyridylamine)

A new unique tetranuclear copper(II) complex doubly-bridged by thiocyanate anions, [Cu4(μ1,3-NCS)6(dpyam)4(O2CH)2(H2O)2 (dpyam = di-2-pyridylamine) has been synthesized and characterized by X-ray diffraction methods and magnetic measurements. The “outer” Cu ions, with a CuN3O(S, O) chromophore, have an axially elongated octahedral geometry. 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 CuN4(S2) chromophore do also have an axially elongated octahedral geometry. The axial positions are occupied by two sulfur atoms of two bridging thiocynate anions (Cu-S semi-coordinating distances are 2.875(1) and 3.126(1) Å). Each Cu ion is bridged by two μ1,3-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.