作者: Guangrui He , Yanhui Hou , Dong Sui , Xiangjian Wan , Guankui Long
DOI: 10.1016/J.TET.2013.05.111
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摘要: Abstract A trifunctional 1,9-dithiophenalenylium salt with benzene spacer has been prepared as the precursor for a phenalenyl-based high spin radical. Electrochemical studies show that this undergoes two three-electron reduction steps and generate its corresponding neutral radical, which studied by quantum chemical calculations. The investigation of density distribution radical revealed electronic properties molecules based on phenalenyl systems are strongly influenced intramolecular topology connection.