Firme Caio L, Antunes O A C, Esteves Pierre M
Universidade Federal do Rio de Janeiro, Instituto de Química, Avenida Athos da Silveira Ramos, 149, CT Bloco A, Sala 622, Cidade UniversitAria, Ilha do Fundão, Rio de Janeiro, BR 21941-909, Brazil.
J Phys Chem A. 2008 Apr 10;112(14):3165-71. doi: 10.1021/jp710606n. Epub 2008 Mar 1.
Nonclassical ions or carbonium ions have multi-center bonding from delocalized sigma or pi electrons. The 2-norbornyl cation, its derivative 6,6-difluoro-2-norbornyl cation, tris-homocyclopropenyl cation, 7-norbornenyl cation, and 4-cyclopentenyl cation and their corresponding silicon analogues were studied in this work. All carbocations have topologically different 3c-2e systems. The magnitude of all delocalization indexes between each atomic pair of the 3c-2e bond can be used to predict homoaromaticity. The silicon analogues have a topologically different 3c-2e bond from their corresponding carbocation.
非经典离子或碳正离子具有由离域的σ或π电子形成的多中心键。本研究工作对2-降冰片基阳离子、其衍生物6,6-二氟-2-降冰片基阳离子、三同环丙烯基阳离子、7-降冰片烯基阳离子和4-环戊烯基阳离子及其相应的硅类似物进行了研究。所有碳正离子都具有拓扑结构不同的3c-2e体系。3c-2e键的每对原子之间的所有离域指数的大小可用于预测同芳香性。硅类似物与其相应的碳正离子具有拓扑结构不同的3c-2e键。