CONTRATADOS
CALVO Rafael
artículos
Título:
A Pyrophosphate-Bridged CuII Chain Magnet {[Na3Cu(P2O7)(NO3)].3H2O}n
Autor/es:
SARTORIS R. P; SANTANA, R. C.; BAGGIO, R. F.; PEÑA, O.; PEREC, M; CALVO. R.
Revista:
INORGANIC CHEMISTRY
Editorial:
AMER CHEMICAL SOC
Referencias:
Lugar: Washington; Año: 2010 vol. 49 p. 5650 - 5650
ISSN:
0020-1669
Resumen:
A CuII-CuII pyrophosphate-bridged compound of formula {[Na3Cu(P2O7)(NO3)] 3 3H2O}n (1) has been characterized. X-ray diffraction measurements show that it crystallizes in the monoclinic space group P21/m, with unit cell dimensions a = 7.2492(5)A°, b = 8.2446(6)A°, c = 9.9050(7)A°, β = 107.123(1)°, and Z = 2. The structure consists of chains of CuII cations at inversion symmetry sites bound to four equatorial oxygen atoms provided by two pyrophosphate anions halved by a symmetry plane and two axial oxygen atoms of nitrate anions. The molar magnetic susceptibility of a powdered sample was measured in the temperature range 2 K < T < 273 K, and an isothermal magnetization curve, M(B0,T), was obtained at T = 30 K, with the magnetic field B0 between 0 and 5 T. Fitting a spinchain model to the susceptibility data, we evaluate an antiferromagnetic exchange coupling 2J = -24.3(1) cm-1 (defined as Hex = -2JSiSj) between CuII neighbors. For any orientation of B0, single-crystal electron paramagneticresonance (EPR) spectra obtained at 9.8 and 33.9 GHz at 300 K display a single signal having a g matrix with orthorhombic symmetry, arising from the merger produced by the exchange interaction of the resonances corresponding to the two rotated CuII sites. The g matrices of the individual molecules calculated assuming axial symmetry yielded principal values g//= 2.367(1) and gper = 2.074(1) at both frequencies, indicating a dx2-y2 ground-state orbital for the CuII ions. The angular variation of the EPR line width suggests exchange narrowing in a system with onedimensional spin dynamics, as expected from the structure and susceptibility data. The results, discussed in terms of the crystal and electronic structures and of the spin dynamics of the compound, are compared with those obtained in other materials