2019RSC AdvancesOpen access

A study on the aromatic conjugation pathways and the ring currents of bridged [18]annulenes

Qimanguli Tuoheti, Ablikim Kerim

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Abstract

The topological resonance energy method was used to investigate the global aromaticity of a set of [18]annulene-derived compounds obtained by replacing two, four, or all six of the inner hydrogen atoms with bridges (oxygen, imino-, sulfur, or combinations of the three).

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The topological resonance energy method was used to investigate the global aromaticity of a set of [18]annulene-derived compounds obtained by replacing two, four, or all six of the inner hydrogen atoms with bridges (oxygen, imino-, sulfur, or combinations of the three).

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Available abstract

The topological resonance energy method was used to investigate the global aromaticity of a set of [18]annulene-derived compounds obtained by replacing two, four, or all six of the inner hydrogen atoms with bridges (oxygen, imino-, sulfur, or combinations of the three).

Key concepts: Annulene, Aromaticity, Ring (chemistry), Chemistry, Chemical shift, Resonance (particle physics), Molecule, Hydrogen bond

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