Transition Metal Complexes of Bidentate and Tridentate Ligands: From Optoelectronic Studies to Supramolecular Assemblies

被引:0
|
作者
Pal, Amlan K. [1 ]
机构
[1] Univ Montreal, Dept Chim, Montreal, PQ H3T 1J4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Density functional theory (DFT); Electrochemistry; NIR emitter; Photochemistry; Supramolecular chemistry; SOLID-STATE; RUTHENIUM COMPLEXES; ELECTRON-TRANSFER; RU(II) COMPLEXES; (MLCT)-M-3 STATE; FACILE ROUTE; GUANIDINIUM; EMISSION; BINDING; 2,2'-BIPYRIDINE;
D O I
10.2533/chimia.2015.659
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This article depicts an overview of some of the research in supramolecular chemistry performed by the author over the past few years. This work includes the synthesis of building blocks, bidentate and tridentate 'super donor' ligands that are comprised of H-hpp (where H-hpp = 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine) coupled with various N-heterocycles as well as the synthesis and characterization of the transition metal complexes in self-assembled superstructures. The article also includes the studies of photophysical, electrochemical and density functional theory calculation of the complexes. Thus, the work relies on a combination of synthetic work and optoelectronic studies, and the results are relevant in the greater context of supramolecular chemistry, solar energy harvesting, and its conversion to chemical energy, photovoltaics and inorganic light-emitting device applications.
引用
收藏
页码:659 / 665
页数:7
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