A Pair of Multifunctional Cu(II)-Dy(III) Enantiomers with Zero-Field Single-Molecule Magnet Behaviors, Proton Conduction Properties and Magneto-Optical Faraday Effects

Multifunctional materials with a coexistence of proton conduction properties, single-molecule magnet (SMM) behaviors and magneto-optical Faraday effects have rarely been reported. Herein, a new pair of Cu(II)-Dy(III) enantiomers, [DyCu2(RR/SS-H2L)2(H2O)4(NO3)2]center dot(NO3)center dot(H2O) (R-1 and S-1) (H4L = [RR/SS] -N,N '-bis [3-hydroxysalicylidene] -1,2-cyclohexanediamine), has been designed and prepared using homochiral Schiff-base ligands. R-1 and S-1 contain linear Cu(II)-Dy(III)-Cu(II) trinuclear units and possess 1D stacking channels within their supramolecular networks. R-1 and S-1 display chiral optical activity and strong magneto-optical Faraday effects. Moreover, R-1 shows a zero-field SMM behavior. In addition, R-1 demonstrates humidity- and temperature-dependent proton conductivity with optimal values of 1.34 x 10-4 S center dot cm-1 under 50 degrees C and 98% relative humidity (RH), which is related to a 1D extended H-bonded chain constructed by water molecules, nitrate and phenol groups of the RR-H2L ligand.

Automated summary

In this study, a new pair of Cu(II)-Dy(III) enantiomers with coexistence of proton conduction properties, single-molecule magnet behaviors, and magneto-optical Faraday effects have been successfully designed and prepared. These materials exhibit chiral optical activity and strong magneto-optical Faraday effects, and demonstrate humidity- and temperature-dependent proton conductivity and single-molecule magnet behavior, which are of significant importance for the construction of multifunctional materials.