E. Colacio et al., A MIXED-BRIDGED CU-3 CLUSTER WITH AN ISOSCELES-TRIANGULAR ARRAY OF COPPER(II) IONS - SYNTHESIS, CRYSTAL-STRUCTURE AND MAGNETIC-PROPERTIES, Journal of the Chemical Society. Dalton transactions, (3), 1995, pp. 343-348
The reaction of H(2)L [H(2)L = N,N'-bis(1,3-dimethyl-5-nitrosopyrimidi
ne-2,4 (1H,3H)-dion-6-yl)propyl-enediamine] with an excess of Cu(ClO4)
(2).6H(2)O in ethanol gave the dinuclear complex [Cu(mu-HL)-Cu(H2O)(2)
(EtOH)][ClO4](3) 1, magnetic studies of which revealed that the antife
rromagnetic exchange interaction mediated by the oximate groups is so
strong that it causes a complete spin coupling at room temperature. Th
is compound reacted with NaCl in ethanol-water (5:1) to afford the mix
ed-bridged trinuclear copper(II) complex [{Cu(mu-HL)Cu(H2O)CU(mu-Cl)][
ClO4](2).4.88H(2)O 2 the crystal structure of which was solved by sing
le-crystal X-ray diffraction. Compound 2 consists of discrete trinucle
ar cations [{Cu(mu-HL)Cu(H2O)Cu(mu-L)}(mu-Cl)](2+), non-co-ordinated p
erchlorate anions and lattice water molecules. Within the trinuclear c
ation, which has C-2, symmetry the three copper ions are arranged at t
he corners of an isosceles triangle. Each terminal copper atom Cu(2)..
.Cu(2) distance of 3.373(4) Angstrom, whereas a chloride anion bridges
the two terminal copper atoms with a Cu(2)...Cu(2) distance of 4.770(
4) Angstrom. The angles Cu(2)-Cu(1)-Cu-2 and Cu(2)-Cl(1)-Cu(2) are 90.
0(1) and 144.4(4)degrees, respectively. The central Cu(1) exhibits a s
quare pyramidal CuO5 co-ordination environment with four oxygen atoms
of oximate groups in the basal plane and the water oxygen at the apica
l site. The terminal Cu(2) atoms occupy the N-4 inner site of the liga
nd with the chloride bridging anion occupying the axial position of th
e square pyramidal CuN4Cl co-ordination environment. From magnetic sus
ceptibility measurements, complex 2 was found to exhibit a very strong
antiferromagnetic exchange interaction through the oximate bridges (J
= -189 cm(-1)), leading to complete spin coupling at 120 K. Magnetic
parameters are discussed on the basis of the structural results and co
mpared with those other related complexes.