Enhancement of Single-Molecule Magnet Properties by Manipulating Intramolecular Dipolar Interactions.

Abstract

A new single-molecule magnet (SMM) complex [K(18-crown-6)][(COT)Er(µ-Cl)3Er(COT)] (Er2Cl3, COT=cyclooctatetraenide dianion) is obtained by the reaction of [(COT)Er(µ-Cl)(THF)]2 (Er2Cl2, THF=tetrahydrofuran) with an equivalent of KCl in the presence of 18-crown-6. The two COT-Er units in the newly formed complex are triply bridged by µ-Cl ligands, leading to the "head-to-tail" alignment of the magnetic easy axes distinctly different from the "staggered" arrangement in the precursor complex. This structural transformation has led to significantly enhanced intramolecular dipolar interactions and a reduced transverse component of the crystal fields, increasing the energy barrier from 150(8) K for Er2Cl2 to 264(4) K for Er2Cl3 and extending its magnetic relaxation time at 2 K by 2500 times with respect to Er2Cl2. More importantly, the blocking temperature increased from lower than 2 K for Er2Cl2 to 8 K for Er2Cl3, and the magnetic hysteresis loops at 2 K changed from butterfly-shaped for Er2Cl2 to open hysteresis loop with coercive force of 7 kOe for Er2Cl3. These results suggest that the properties of SMMs can be effectively tuned and improved by rationally arranging magnetic spins via molecular engineering.