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Fabrication Procedures and Birefringence Measurements for Designing Magnetically Responsive Lanthanide Ion Chelating Phospholipid Assemblies
Published on: January 3, 2018
Layered lanthanide phosphonates Ln(2-qpH)(SO4)(H2O)2 (Ln = La, Ce, Pr, Nd, Sm): polymorphism and magnetic properties
Xiu-Fang Ma1, Dai Zeng1,2, Chang Xu1
1State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Advanced Microstructures, Nanjing University, Nanjing 210023, P. R. China. lmzheng@nju.edu.cn.
Abstract:
Polymorphic layered lanthanide coordination polymers provide opportunities to study the effect of intralayer and interlayer interactions on their magnetic dynamics. Herein we report a series of layered lanthanide phosphonates, namely, α-Ln(2-qpH)(SO4)(H2O)2 (Ln = Sm) (α-Ln), β-Ln(2-qpH)(SO4)(H2O)2 (Ln = Pr, Nd, Sm) (β-Ln) and γ-Ln(2-qpH)(SO4)(H2O)2 (Ln = La, Ce, Pr, Nd, Sm) (γ-Ln) (2-qpH2 = 2-quinolinephosphonic acid), which crystallize in monoclinic P21/c (α-Ln), triclinic P1̄ (β-Ln) and orthorhombic Pbca (γ-Ln) space groups, respectively. The structural differences between the β- and γ-phases lie not only in the intralayer but also in the interlayer. Within the layers, the Ln2O2 dimers are aligned parallel in the β-phase, but are non-parallel in the γ-phase. In the interlayer, there are π-π interactions between the quinoline groups in the α- and β-phases but not in the γ-phase. Magnetic studies reveal a field-induced slow relaxation of the magnetisation at low temperatures for compounds γ-Ce, β-Nd, and γ-Nd, and the impact of polymorphism on the magnetic dynamics of Nd(III) compounds is discussed.
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