Literature DB >> 25858673

Quantifying aromaticity with electron delocalisation measures.

Ferran Feixas1, Eduard Matito, Jordi Poater, Miquel Solà.   

Abstract

Aromaticity cannot be measured directly by any physical or chemical experiment because it is not a well-defined magnitude. Its quantification is done indirectly from the measure of different properties that are usually found in aromatic compounds such as bond length equalisation, energetic stabilisation, and particular magnetic behaviour associated with induced ring currents. These properties have been used to set up the myriad of structural-, energetic-, and magnetic-based indices of aromaticity known to date. The cyclic delocalisation of mobile electrons in two or three dimensions is probably one of the key aspects that characterise aromatic compounds. However, it has not been until the last decade that electron delocalisation measures have been widely employed to quantify aromaticity. Some of these new indicators of aromaticity such as the PDI, FLU, ING, and INB were defined in our group. In this paper, we review the different existing descriptors of aromaticity that are based on electron delocalisation properties, we compare their performance with indices based on other properties, and we summarise a number of applications of electronic-based indices for the analysis of aromaticity in interesting chemical problems.

Entities:  

Year:  2015        PMID: 25858673     DOI: 10.1039/c5cs00066a

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  27 in total

1.  Evaluating Computational and Structural Approaches to Predict Transformation Products of Polycyclic Aromatic Hydrocarbons.

Authors:  Ivan A Titaley; Daniel M Walden; Shelby E Dorn; O Maduka Ogba; Staci L Massey Simonich; Paul Ha-Yeon Cheong
Journal:  Environ Sci Technol       Date:  2019-01-22       Impact factor: 9.028

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

Authors:  Caio Lima Firme; Diógenes Mendes Araújo
Journal:  J Mol Model       Date:  2017-08-07       Impact factor: 1.810

3.  Evaluation of Slight Changes in Aromaticity through Electronic and Density Functional Reactivity Theory-Based Descriptors.

Authors:  Rodrigo Báez-Grez; Ricardo Pino-Rios
Journal:  ACS Omega       Date:  2022-06-13

4.  3D and 2D aromatic units behave like oil and water in the case of benzocarborane derivatives.

Authors:  Jordi Poater; Clara Viñas; Miquel Solà; Francesc Teixidor
Journal:  Nat Commun       Date:  2022-07-04       Impact factor: 17.694

5.  Validation of the recently developed aromaticity index D3BIA for benzenoid systems. Case study: acenes.

Authors:  Diógenes Mendes Araújo; Tamires Ferreira da Costa; Caio Lima Firme
Journal:  J Mol Model       Date:  2015-09-02       Impact factor: 1.810

6.  Double C-H bond activation of acetylene by atomic boron in forming aromatic cyclic-HBC2BH in solid neon.

Authors:  Jiwen Jian; Wei Li; Xuan Wu; Mingfei Zhou
Journal:  Chem Sci       Date:  2017-04-19       Impact factor: 9.825

7.  Rationalizing the relative abundances of trimetallic nitride template-based endohedral metallofullerenes from aromaticity measures.

Authors:  M Garcia-Borràs; S Osuna; J M Luis; M Solà
Journal:  Chem Commun (Camb)       Date:  2017-04-06       Impact factor: 6.222

8.  Why Aromaticity Is a Suspicious Concept? Why?

Authors:  Miquel Solà
Journal:  Front Chem       Date:  2017-03-24       Impact factor: 5.221

9.  "Bottled" spiro-doubly aromatic trinuclear [Pd2Ru]+ complexes.

Authors:  Maksim Kulichenko; Nikita Fedik; Anna Monfredini; Alvaro Muñoz-Castro; Davide Balestri; Alexander I Boldyrev; Giovanni Maestri
Journal:  Chem Sci       Date:  2020-10-23       Impact factor: 9.825

10.  Learning a Local-Variable Model of Aromatic and Conjugated Systems.

Authors:  Matthew K Matlock; Na Le Dang; S Joshua Swamidass
Journal:  ACS Cent Sci       Date:  2018-01-03       Impact factor: 14.553

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