Literature DB >> 28785890

D2BIA-flexible, not (explicitly) arbitrary and reference/structurally invariant-a very effective and improved version of the D3BIA aromaticity index.

Caio Lima Firme1, Diógenes Mendes Araújo2.   

Abstract

Although there are a multitude of aromaticity indexes, only a few have a widespread usage. All famous aromaticity indexes are limited: HOMA and FLU are reference-dependent; ELF is π-bond-dependent; PDI is structurally dependent and NICS is ring size dependent. These limitations stimulate the continuous search for better (i.e., having no dependency), more flexible (i.e., applied to any aromatic system) and more effective (i.e., with excellent correlations with other indexes) aromaticity indexes. The D3BIA was our first topological aromaticity index. It is flexible, reference-independent and effective for planar and caged aromatic molecules. However, one of its terms, the degree of degeneracy (δ), is arbitrary and difficult to carry out for new users. Thus, in this work, we show that D2BIA-an improved version of D3BIA-is a good candidate to be used widely, since it retains the strong points of D3BIA while avoiding its weak point. In particular cases where all studied systems have δ = 1 (e.g., for acenes), then D2BIA equals D3BIA. For our recent study with acenes, D3BIA (and, as a consequence, D2BIA) has (have) an excellent correlation with FLU according to the MP3 method. In this work, by using DFT calculations for a series involving several six-membered and five-membered heteroaromatic rings, only D2BIA and NICS have very good correlation. All other well known aromaticity indexes used in this work (FLU, HOMA and ELF) gave poor correlations. As to homoaromatic systems, only D2BIA vs NICS and D2BIA vs FLU plots have excellent correlations. HOMA has the worst results in this series. Thus, D2BIA proved to be flexible and effective for the analysis of heteroaromatic rings of different sizes and for caged homoaromatic systems. Moreover, D2BIA has better correlations than D3BIA for planar aromatic systems, and same correlations for caged-homoaromatic systems. Graphical abstract D2BIA-an effective and improved version of the D3BIA aromaticity index.

Entities:  

Keywords:  Aromaticity index; D2BIA; D3BIA; Heteroaromatic rings; Homoaromaticity; NICS; QTAIM

Year:  2017        PMID: 28785890     DOI: 10.1007/s00894-017-3433-6

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


  27 in total

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3.  Quantifying aromaticity with electron delocalisation measures.

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5.  Analysis of electron delocalization in aromatic systems: individual molecular orbital contributions to para-delocalization indexes (PDI).

Authors:  Mireia Güell; Eduard Matito; Josep M Luis; Jordi Poater; Miquel Solà
Journal:  J Phys Chem A       Date:  2006-10-12       Impact factor: 2.781

6.  Is Al2Cl6 aromatic? Cautions in superficial NICS interpretation.

Authors:  Juan José Torres; Rafael Islas; Edison Osorio; Jason G Harrison; William Tiznado; Gabriel Merino
Journal:  J Phys Chem A       Date:  2013-06-24       Impact factor: 2.781

7.  Minimizing the risk of reporting false aromaticity and antiaromaticity in inorganic heterocycles following magnetic criteria.

Authors:  Juan J Torres-Vega; Alejandro Vásquez-Espinal; Julio Caballero; María L Valenzuela; Luis Alvarez-Thon; Edison Osorio; William Tiznado
Journal:  Inorg Chem       Date:  2014-03-17       Impact factor: 5.165

8.  The non-covalent nature of the molecular structure of the benzene molecule.

Authors:  Thiago Messias Cardozo; Felipe Fantuzzi; Marco Antonio Chaer Nascimento
Journal:  Phys Chem Chem Phys       Date:  2014-06-14       Impact factor: 3.676

9.  Electronic structures of bisnoradamantenyl and bisnoradamantanyl dications and related species.

Authors:  Caio L Firme; Tamires F da Costa; Eduardo T da Penha; Pierre M Esteves
Journal:  J Mol Model       Date:  2013-02-28       Impact factor: 1.810

10.  Sigma-pi separation of the electron localization function and aromaticity.

Authors:  J C Santos; W Tiznado; R Contreras; P Fuentealba
Journal:  J Chem Phys       Date:  2004-01-22       Impact factor: 3.488

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