Aromaticity and Chirality: New Facets of Old Concepts

The review summarizes the results of previous and the latest studies on aromaticity and related concepts. The electron counting rule for 3D-aromatic systems 2(n + 1)<sup>2</sup> is shown to be a generalization of the 4n + 2 rule for planar molecules, and, vice versa, the latter can be de...

Full description

Saved in:
Bibliographic Details
Main Author: Bagrat A. Shainyan
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/29/22/5394
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846152764326936576
author Bagrat A. Shainyan
author_facet Bagrat A. Shainyan
author_sort Bagrat A. Shainyan
collection DOAJ
description The review summarizes the results of previous and the latest studies on aromaticity and related concepts. The electron counting rule for 3D-aromatic systems 2(n + 1)<sup>2</sup> is shown to be a generalization of the 4n + 2 rule for planar molecules, and, vice versa, the latter can be derived from the former. The relative stability of the push–pull and captodative aromatic systems is shown to depend on the nature of the groups separated by the C=C bond in geminal or vicinal positions. The fully symmetrical molecules of hexamethylbenzene and hexacyanobenzene were studied using structural, energetic, and NMR criteria, and the donor substituents were shown to increase the aromaticity. Taking into account the coincidence of the number of π-electrons in aromatic systems with the number of electrons on the filled electron subshells (s, p, d, and f) and considering electrons as objects in a space of states allowed to conclude that no g-elements can exist and that the extension of the Periodic Table is possible only by filling 6f, 7d, or 8s subshells. The dimensionality of space also affects the chirality of molecules, making planar or even linear molecules chiral on oriented surfaces, which can be used for the preparation of enantiomerically pure drugs, resolution of prochiral compounds, etc.
format Article
id doaj-art-1d71a43c7c2d453583a1e6b4a490c8a4
institution Kabale University
issn 1420-3049
language English
publishDate 2024-11-01
publisher MDPI AG
record_format Article
series Molecules
spelling doaj-art-1d71a43c7c2d453583a1e6b4a490c8a42024-11-26T18:15:49ZengMDPI AGMolecules1420-30492024-11-012922539410.3390/molecules29225394Aromaticity and Chirality: New Facets of Old ConceptsBagrat A. Shainyan0Institute of Chemistry, Siberian Division of the Russian Academy of Sciences, 1 Favorsky Street, 664033 Irkutsk, RussiaThe review summarizes the results of previous and the latest studies on aromaticity and related concepts. The electron counting rule for 3D-aromatic systems 2(n + 1)<sup>2</sup> is shown to be a generalization of the 4n + 2 rule for planar molecules, and, vice versa, the latter can be derived from the former. The relative stability of the push–pull and captodative aromatic systems is shown to depend on the nature of the groups separated by the C=C bond in geminal or vicinal positions. The fully symmetrical molecules of hexamethylbenzene and hexacyanobenzene were studied using structural, energetic, and NMR criteria, and the donor substituents were shown to increase the aromaticity. Taking into account the coincidence of the number of π-electrons in aromatic systems with the number of electrons on the filled electron subshells (s, p, d, and f) and considering electrons as objects in a space of states allowed to conclude that no g-elements can exist and that the extension of the Periodic Table is possible only by filling 6f, 7d, or 8s subshells. The dimensionality of space also affects the chirality of molecules, making planar or even linear molecules chiral on oriented surfaces, which can be used for the preparation of enantiomerically pure drugs, resolution of prochiral compounds, etc.https://www.mdpi.com/1420-3049/29/22/5394aromaticityelectron-counting ruleschiralitydimensionality of spaceboundaries of the Periodic Table of the Elements
spellingShingle Bagrat A. Shainyan
Aromaticity and Chirality: New Facets of Old Concepts
Molecules
aromaticity
electron-counting rules
chirality
dimensionality of space
boundaries of the Periodic Table of the Elements
title Aromaticity and Chirality: New Facets of Old Concepts
title_full Aromaticity and Chirality: New Facets of Old Concepts
title_fullStr Aromaticity and Chirality: New Facets of Old Concepts
title_full_unstemmed Aromaticity and Chirality: New Facets of Old Concepts
title_short Aromaticity and Chirality: New Facets of Old Concepts
title_sort aromaticity and chirality new facets of old concepts
topic aromaticity
electron-counting rules
chirality
dimensionality of space
boundaries of the Periodic Table of the Elements
url https://www.mdpi.com/1420-3049/29/22/5394
work_keys_str_mv AT bagratashainyan aromaticityandchiralitynewfacetsofoldconcepts