Relationship of charge to antiaromaticity in bis-fluorenyl dications and fluorenyl monocations: experimental support for theoretical calculations
作者： Nancy S. Mills , Sean P. McClintock
DOI: 10.1039/C2CC33799A
关键词: Antiaromaticity 、 Delocalized electron 、 Computational chemistry 、 Charge (physics) 、 Chemistry 、 Chemical shift
摘要: The antiaromaticity of fluorenyl cations is dependent on the magnitude charge system. Theoretical assessments and were supported by experimental NMR chemical shifts. Delocalization was related to antiaromaticity, evaluated through standard deviation charges carbons systems.
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