Reversible on-off switching of Dy(III) single-molecule magnets via single-crystal-to-single-crystal transformation.

While the interest in single-molecule magnets (SMMs) lies in their potential applications in information storage and quantum computing, the switching of their slow magnetic relaxation associated with dynamic crystal-to-crystal transformation is insufficiently exploited. Herein, three pentagonal-bipyramidal (PBP) Dy(III) complexes, [Dy(Bcpen)(Cl) 3 ] (1), [Dy(Bcpen)(OPhCl 2 NO 2 ) 3 ] (2) and [Dy(Bcpen)(OPhCl 2 NO 2 ) 3 ]·0.5CH 3 CN (2·CH3CN), are successfully assembled, and structurally and magnetically studied (Bcpen = N , N -bis(4-chloro-2-methylenepyridinyl) ethylenediamine and Cl 2 NO 2 PhOH = 2,6-dichloro-4-nitrophenol). The molecular characteristics and magnetic properties of complexes 2 and 2·CH3CN, constructed with the motivation of modulating a magnetic switch by external stimuli, are systematically explored. Dramatically, 2 and 2·CH3CN can mutually transform through reversible single-crystal-to-single-crystal (SCSC) conversion associated with the capture and release of guest CH 3 CN molecules, resulting in an infrequent on/off switching of PBP Dy(III) molecule-based magnets. Further measurements on the desolvated and resolvated samples, complexes 2-re and 2·CH3CN-re, confirm the fascinating transformation processes. The magneto-structural relationship has been rationally investigated and discussed with ab initio calculations as well.