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1D Chains of Lanthanoid Ions and a Dithienylethene Ligand Showing Slow Relaxation of the Magnetization

机译:镧系元素离子和二噻吩基乙烯配体的一维链显示出磁化的缓慢弛豫

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Three isostructural 1D lanthanoid complexes with the general formula {[Ln 2 (DTE)(H-DTE)(MeOH) 2 ]·2H 2 O} n (Ln = Tb, Dy, and Yb; DTE = 1,2-bis(5-carboxyl-2-methyl-3-thienyl) perfluorocyclopentene) were synthesized. In the 1D chain structure of each complex, lanthanide ions are seven coordinate with a capped trigonal prism geometry. The 1,2-bis(5-carboxyl-2-methyl-3-thienyl) perfluorocyclopentene (DTE) ligand adopts a parallel configuration in these complexes, which results in the loss of the photo-isomerization ability of the ligand. From magnetic measurements, each complex undergoes slow relaxation of the magnetization via multiple processes in a dc field.
机译:三个具有通式{[Ln 2(DTE)(H-DTE)(MeOH)2]·2H 2 O} n(Ln = Tb,Dy和Yb; DTE = 1,2-bis(合成了5-羧基-2-甲基-3-噻吩基)。在每个复合物的一维链结构中,镧系元素离子为七个坐标,且具有封顶的三角棱镜几何形状。 1,2-双(5-羧基-2-甲基-3-噻吩基)全氟环戊烯(DTE)配体在这些配合物中采用平行构型,导致配体的光异构化能力下降。从磁测量结果来看,每个复合物都会通过直流场中的多个过程缓慢地磁化松弛。

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