Hysteresis Photomodulation via Single-Crystal-to-Single-Crystal Isomerization of a Photochromic Chain of Dysprosium Single-Molecule Magnets

摘要

A one-dimensional coordination solid 1_c is synthesized by reaction of a bispyridyl dithienylethene (DTE) photochromic unit with the highly anisotropic dysprosium-based single-molecule magnet [Dy(Tp~(py))F-(pyridine)_2]PF_6. Slow magnetic relaxation characteristics are retained in the chain compound 1_c and photoisomerization of the bridging DTE ligand induces a single-crystal-to-single-crystal transformation that can be monitored using photocrystallography. Notably, the resulting chain compound 1_ο exhibits faster low-temperature relaxation than that of 1_c which is apparent in magnetic hysteresis data collected for both compounds as high as 4 K Ab initio calculations suggest that this photomodulation of the magnetic relaxation behavior is due to crystal packing changes rather than changes to the crystal field splitting upon ligand isomerization.