Tatyana V. Balashova,Svetlana K. Polyakova,Vasily A. Ilichev,E.V. Baranov,Georgy K. Fukin,Konstantin A. Kozhanov,Grigory Zhigulin,Sergey Yu. Ketkov,M.N. Bochkarev
出处
期刊:Organometallics [American Chemical Society] 日期:2023-11-03卷期号:42 (22): 3283-3291被引量:3
标识
DOI:10.1021/acs.organomet.3c00388
摘要
The potassium salt of the perylene ligand used as a precursor in further transformations was obtained by the reduction of perylene with potassium metal in DME or THF. The perylene ligand was transferred to a samarium metal center using a metathesis strategy, yielding a complex SmI(Per)(THF)4. In the resulting compound, samarium remains divalent, while perylene is in the form of a radical anion, which is confirmed by spectroscopic methods and quantum chemical calculations.