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碳正离子及其硅类似物的电子性质。

Electronic nature of carbonium ions and their silicon analogues.

作者信息

Firme Caio L, Antunes O A C, Esteves Pierre M

机构信息

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.

出版信息

J Phys Chem A. 2008 Apr 10;112(14):3165-71. doi: 10.1021/jp710606n. Epub 2008 Mar 1.

Abstract

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.

摘要

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。

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