Dysprosium Heteroleptic Corrole-Phthalocyanine Triple-Decker Complexes: Synthesis, Crystal Structure, and Electrochemical and Magnetic Properties.
Guifen LuCheng HeKang WangJunshan SunDongdong QiLei GongChiming WangZhongping OuSen YanShuyuan ZengWeihua ZhuPublished in: Inorganic chemistry (2017)
Two triple-decker dinuclear sandwich dysprosium complexes, which are represented as Dy2[Pc(OC5H11)8]2[Cor(FPh)3] (1) and Dy2[Pc(OC5H11)8]2[Cor(ClPh)3] (2), were synthesized and characterized by spectroscopic and electrochemical methods in nonaqueous media. Their electronic structures were also investigated on the basis of TD-DFT calculations. The sandwich triple-decker nature with the molecular conformation of [Pc(OC5H11)8]Dy[Cor(FPh)3]Dy[Pc(OC5H11)8] for compound 1 was unambiguously revealed by single-crystal X-ray diffraction analysis and showed each dyprosium ion to be octacoordinated by the isoindole and pyrrole nitrogen atoms of an outer phthalocyanine ring and the central corrole ring, respectively. In addition, the magnetic properties of both compounds have also been characterized for exploring the functionalities of these types of triple-decker complexes.
Keyphrases
- single molecule
- crystal structure
- atomic force microscopy
- molecularly imprinted
- photodynamic therapy
- gold nanoparticles
- high resolution
- molecular docking
- density functional theory
- molecular dynamics simulations
- ionic liquid
- molecular dynamics
- magnetic resonance
- label free
- computed tomography
- solid phase extraction
- capillary electrophoresis
- amino acid