Lanthanide-directed synthesis of luminescent self-assembly supramolecular structures and mechanically bonded systems from acyclic coordinating organic ligands

被引:237
作者
Barry, Dawn E. [1 ]
Caffrey, David F.
Gunnlaugsson, Thorfinnur [1 ]
机构
[1] Univ Dublin Trinity Coll, Sch Chem, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
SINGLE-MOLECULE MAGNET; QUANTITATIVELY ADDRESSING COOPERATIVITY; CIRCULARLY-POLARIZED LUMINESCENCE; INTERLOCKED MACROCYCLIC LIGANDS; TRIDENTATE NITROGEN LIGANDS; SIMPLE THERMODYNAMIC MODEL; TRIPLE-HELICAL COMPLEXES; HIGHLY LUMINESCENT; PHOTOPHYSICAL PROPERTIES; TEMPLATE SYNTHESIS;
D O I
10.1039/c6cs00116e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein some examples of the use of lanthanide ions (f-metal ions) to direct the synthesis of luminescent self-assembly systems (architectures) will be discussed. This area of lanthanide supramolecular chemistry is fast growing, thanks to the unique physical (magnetic and luminescent) and coordination properties of the lanthanides, which are often transferred to the resulting supermolecule. The emphasis herein will be on systems that are luminescent, and hence, generated by using either visibly emitting ions (such as Eu-III, Tb-III and Sm-III) or near infrared emitting ions (like Nd-III, Yb-III and Er-III), formed through the use of templating chemistry, by employing structurally simple ligands, possessing oxygen and nitrogen coordinating moieties. As the lanthanides have high coordination requirements, their use often allows for the formation of coordination compounds and supramolecular systems such as bundles, grids, helicates and interlocked molecules that are not synthetically accessible through the use of other commonly used templating ions such as transition metal ions. Hence, the use of the rare-earth metal ions can lead to the formation of unique and stable species in both solution and in the solid state, as well as functional and responsive structures.
引用
收藏
页码:3244 / 3274
页数:31
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