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

Author:

Zhu Shui-Dong1ORCID,Zhou Yu-Lin1,Liu Fang1,Lei Yu1,Liu Sui-Jun2ORCID,Wen He-Rui2,Shi Bin1,Zhang Shi-Yong1,Liu Cai-Ming3ORCID,Lu Ying-Bing1

Affiliation:

1. College of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou 341000, China

2. Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China

3. Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Chinese Academy of Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

Abstract

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]·(NO3)·(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 × 10−4 S·cm−1 under 50 °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.

Funder

NSF of China

NSF of Jiangxi Provincial Education Department

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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