Azido-cobalt(II) coordination polymers exhibiting slow magnetic relaxation and metamagnetic transition

Abstract

Abstract Two coordination polymers of mono-dimensional doubly bridged-azido-cobalt(II) complexes catena-[Co(2,6-lutidine-N-oxide)(μ1,1-N3)2] (1) and catena-{[Co(μ1,1-N3)2(H2O)2](3-picoline-N-oxide)2} (2), where 2,6-lutidine-N-oxide\u202f=\u202f2,6-dimethylpyridine-N-oxide and 3-picoline-N-oxide\u202f=\u202f3-methylpyridine-N-oxide, were synthesized, and structurally characterized by single crystal X-ray crystallography. The Co(II) cations in complexes 1 and 2 are penta- and hexa-coordinate, respectively with four μ1,1-bridging azido groups and a terminal 2,6-lutidine-N-oxide molecule in 1 or two trans aqua molecules in 2. Magnetic relaxations in the zero field are consistent with single chain magnetic behavior (SCM) and the ac susceptibility measurements revealed that the weak ferromagnetic exchanges in the two complexes are associated with slow relaxation of magnetization. Complex 2 exhibits metamagnetic transition with an antiferromagnetic phase transition at 12\u202fK at the applied field of 200\u202fOe.