α-氨基酸衍生的(1,2,3-三唑-4-基)-吡啶酰胺(tzpa)配体及其相应发光Tb(iii)配合物的合成†

Isabel N. Hegarty , Chris S. Hawes , Thorfinnur Gunnlaugsson
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引用次数: 0

摘要

介绍了将两种已知配体结构的配位性质结合在一个单元内设计的手性α-氨基酸衍生的(1,2,3-三唑-4-基)-吡啶酰胺(tzpa)配体4-6的合成。通过探测配体的基态和单线态激发态性质以及监测长波长下Tb(iii)发射的演变,研究了这些配体和镧系离子Tb(iii)在溶液中的自组装形成。光谱结果表明,在热力学控制下 : 3(Tb : L) 然后使用非线性回归分析对滴定数据的分析表明,溶液中的主要物种是 : 2(Tb : L) 在加入0.5当量的Tb(iii)之后。
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Synthesis of α-amino acid derived (1,2,3-triazol-4-yl)-picolinamide (tzpa) ligands and their corresponding luminescent Tb(iii) complexes†

The synthesis of chiral α-amino acid derived (1,2,3-triazol-4-yl)-picolinamide (tzpa) ligands 4–6 designed by combining the coordination properties of two well-known ligand structures within a single unit is described. The self-assembly formation between these ligands and the lanthanide ion Tb(iii) was investigated in solution by probing the ground and the singlet excited state properties of the ligands as well as monitoring the evolution of the Tb(iii) emission at long wavelengths. The spectroscopic results showed that while under thermodynamic control the 1 : 3 (Tb : L) is produced, then analysis of the titration data using non-liner regression analysis demonstrated that the main species in solution is the 1 : 2 (Tb : L) after the addition of 0.5 equivalents of Tb(iii).

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