Luminescent DyIII single ion magnets with same N6O3 donor atoms but different donor atom arrangements, ‿span style='font-style: italic'>fac‿[DyIII(HLDL-ala)3]·8H2O and ‿sp
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Two DyIII complexes with same N6O3 donor atoms but different donor atom arrangements ‘fac’-[DyIII(HLDL-ala)3]·8H2O (class="boldFont">1) and ‘mer’-[DyIII(HLDL-phe)3]·7H2O (class="boldFont">2) were synthesized, where H2LDL-ala and H2LDL-phe are tridentate NNO ligands of N-[(imidazol-4-yl)methylidene]-class="smallcaps">dl-alanine and N-[(imidazol-4-yl)methylidene]-class="smallcaps">dl-phenylalanine, respectively. Each DyIII ion is coordinated by three mono-deprotonated mono-negative NNO tridentate ligands to form a nona-coordination geometry of a tricapped trigonal prism (TTP). class="boldFont">1 consists of enantiomers ‘fac’-[DyIII(HLD-ala)3] and ‘fac’-[DyIII(HLL-ala)3], while class="boldFont">2 consists of ‘mer’-[DyIII(HLD-phe)2(HLL-phe)] and ‘mer’-[DyIII(HLD-phe)(HLL-phe)2]. The temperature dependence of the magnetic susceptibilities and field-dependence of the magnetization of two complexes showed the different magnetic profiles and the Stark splitting of the ground state 6H15/2 due to the crystal field effect on DyIII ion (4f9, J = 15/2, S = 5/2, L = 5, gJ = 4/3, 6H15/2). Luminescence spectra were observed and the fine structures assigned to the 4F9/2 → 6H15/2 transitions are partially observed. class="boldFont">1 and class="boldFont">2 showed an out-of-phase signal with frequency-dependence in alternating current (ac) susceptibility under a dc bias field of 1000 Oe, indicative of field induced single ion magnet (SIM). The ac magnetic susceptibilities under 1000 Oe dc field of class="boldFont">2 showed the maximum peaks at the higher temperature than those of class="boldFont">1, indicating that the energy barrier of class="boldFont">2 is larger than that of class="boldFont">1.

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