Zero-Field Slow Magnetic Relaxation in Binuclear Dy Acetylacetonate Complex with Pyridine-N-Oxide

Abstract

A new complex [Dy(C5H7O2)3(C5H5NO)]2·2CHCl3 (1) has been synthesized by the reaction of pyridine-N-oxide with dysprosium (III) acetylacetonate in an n-heptane/chloroform mixture (1/20). X-ray data show that each dysprosium atom is chelate-like coordinated by three acetylacetonate ligands and the oxygen atom from two bridging molecules of pyridine-N-oxide, which unite the dysprosium atoms into a binuclear complex. Static (constant current) and dynamic (alternating current) investigations and ab initio calculations of the magnetic properties of complex 1 were performed. The complex was shown to exhibit a frequency maximum under alternating current. At temperatures above 10 K, the maximum shifts to a higher frequency, which is characteristic of SMM behavior. It is established that the dependence of ln(τ) on 1/T for the relaxation process is nonlinear, which indicates the presence of Raman relaxation mechanisms, along with the Orbach mechanism.

Keywords

• single molecule magnets
• complexes of rare earth metals
• pyridine-N-oxide
• X-ray diffraction analysis
• IR-spectroscopy
• magnetometry