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Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?

In this work the relationship between the formal number of π‐electrons, d‐orbital conjugation topology, π‐electron delocalization and aromaticity in d‐block metallacycles is investigated in the context of recent findings concerning the correlation of π‐HOMO topology and the magnetic aromaticity indi...

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Autores principales: Szczepanik, Dariusz W., Solà, Miquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382291/
https://www.ncbi.nlm.nih.gov/pubmed/30828509
http://dx.doi.org/10.1002/open.201900014
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author Szczepanik, Dariusz W.
Solà, Miquel
author_facet Szczepanik, Dariusz W.
Solà, Miquel
author_sort Szczepanik, Dariusz W.
collection PubMed
description In this work the relationship between the formal number of π‐electrons, d‐orbital conjugation topology, π‐electron delocalization and aromaticity in d‐block metallacycles is investigated in the context of recent findings concerning the correlation of π‐HOMO topology and the magnetic aromaticity indices in these species. It is demonstrated that for π‐electron rich d‐metallacycles the direct link between aromaticity, the number of π‐electrons and the frontier π‐orbital topology does not strictly hold and for such systems it is very difficult to unambiguously associate their aromaticity with the “4n+2” (Hückel) and “4n” (Möbius) rules. It is also shown that the recently proposed electron density of delocalized bonds (EDDB) method can successfully be used not only to quantify and visualize aromaticity in such difficult cases, but also – in contrast to magnetic aromaticity descriptors – to provide a great deal of information on the real role of d‐orbitals in metallacycles without the ambiguity of bookkeeping of electrons in the π‐subsystem of the molecular ring. Interestingly, some of the metallacycles studied cannot be classified exclusively as Hückel or Möbius because they have a hybrid Hückel‐Möbius or even quasi‐aromatic nature.
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spelling pubmed-63822912019-03-01 Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic? Szczepanik, Dariusz W. Solà, Miquel ChemistryOpen Full Papers In this work the relationship between the formal number of π‐electrons, d‐orbital conjugation topology, π‐electron delocalization and aromaticity in d‐block metallacycles is investigated in the context of recent findings concerning the correlation of π‐HOMO topology and the magnetic aromaticity indices in these species. It is demonstrated that for π‐electron rich d‐metallacycles the direct link between aromaticity, the number of π‐electrons and the frontier π‐orbital topology does not strictly hold and for such systems it is very difficult to unambiguously associate their aromaticity with the “4n+2” (Hückel) and “4n” (Möbius) rules. It is also shown that the recently proposed electron density of delocalized bonds (EDDB) method can successfully be used not only to quantify and visualize aromaticity in such difficult cases, but also – in contrast to magnetic aromaticity descriptors – to provide a great deal of information on the real role of d‐orbitals in metallacycles without the ambiguity of bookkeeping of electrons in the π‐subsystem of the molecular ring. Interestingly, some of the metallacycles studied cannot be classified exclusively as Hückel or Möbius because they have a hybrid Hückel‐Möbius or even quasi‐aromatic nature. John Wiley and Sons Inc. 2019-02-20 /pmc/articles/PMC6382291/ /pubmed/30828509 http://dx.doi.org/10.1002/open.201900014 Text en ©2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers
Szczepanik, Dariusz W.
Solà, Miquel
Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title_full Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title_fullStr Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title_full_unstemmed Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title_short Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
title_sort electron delocalization in planar metallacycles: hückel or möbius aromatic?
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382291/
https://www.ncbi.nlm.nih.gov/pubmed/30828509
http://dx.doi.org/10.1002/open.201900014
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