Synthesis, structures and optical properties of mononuclear La, Eu and Tb complexes supported by calix[4]arene ligands bearing three pendant salicylaldiminato arms

被引:0
作者
Guenzel, Lennart [1 ]
Boerner, Martin [1 ]
Kersting, Berthold [1 ]
机构
[1] Univ Leipzig, Inst Anorgan Chem, Johannisallee 29, D-04103 Leipzig, Germany
来源
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE | 2024年 / 650卷 / 03期
关键词
Calix[4]arenes; salicylaldiminato ligands; lanthanide complexes; X-ray crystal structure; photoluminescence; EQUILIBRIUM-CONSTANTS; EXTRACTION; DIGLYCOLAMIDE; COORDINATION; LANTHANIDES; LUMINESCENCE; CHEMISTRY; ION;
D O I
10.1002/zaac.202300225
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and complexation behaviour of a new calix[4]arene ligand H4L3 bearing three pendant salicylaldimine arms towards selected lanthanide ions has been investigated. Reaction of H4L3 with Ln(NO3)3 & sdot;6H2O in MeOH in the presence of NEt3 provides monomeric complexes of composition [Ln(HL3)] (Ln=La3+ (4), Eu3+ (5), Tb3+ (6)). An X-ray crystallographic analysis for 4 reveals that only two of the three ligand arms are involved in the coordination of the lanthanide ions, to give eight-coordinated Ln3+ ions in a distorted square-antiprismatic N2O6 environment. UV-vis spectrophotometric titrations show that such monomeric species prevail in CH2Cl2/MeOH (1/1 v/v) solution. The apparent stability constants determined by UV-vis spectrophotometric titration are log K=6.8(2) for 5 and log K=5.8(1) for 6. The Eu and Tb complexes luminesce only weakly at 77 K with luminescence lifetimes of 0.469 and 0.306 s. image
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