posted on 2006-11-27, 00:00authored byJung Hee Yoon, Jeong Hak Lim, Hyoung Chan Kim, Chang Seop Hong
Two cyanide-bridged W<sup>V</sup>−M [M = Mn<sup>III</sup> (<b>1</b>), Co<sup>II</sup> (<b>2</b>)] bimetallic
clusters were prepared by self-assembling a new molecular
precursor [W(CN)<sub>6</sub>(bpy)]<sup>-</sup> and the corresponding metal complexes.
Compound <b>1</b> shows a tetranuclear W<sub>2</sub>Mn<sub>2</sub> entity, consisting of a
Jahn−Teller ion, Mn<sup>III</sup>, which serves as an anisotropic source, while
compound <b>2</b> exhibits a trimeric W<sub>2</sub>Co structure. Among them,
compound <b>1</b> displays slow relaxation of the magnetization, which
is typical of a single-molecule magnet behavior.