| Texto completo | |
| Autor(es): Mostrar menos - |
Salles, Guilherme A.
;
Magalhaes, Paulo R. C.
;
Carvalho, Jhonatas R.
;
Maximo-Canadas, Matheus
;
Rosa, Nathalia M. P.
;
Chagas, Julio C. V.
;
Ferrao, Luiz F. A.
;
Aquino, Adelia J. A.
;
Borges, Itamar
;
Machado, Francisco B. C.
;
Lischka, Hans
Número total de Autores: 11
|
| Tipo de documento: | Artigo Científico |
| Fonte: | CHEMISTRY-SWITZERLAND; v. 7, n. 6, p. 19-pg., 2025-11-07. |
| Resumo | |
Polycyclic aromatic hydrocarbons (PAHs) play a central role in materials science due to their extended pi-conjugated systems, with their stability and reactivity depending critically on their aromatic character. In this work, we systematically investigated the aromaticity and stability of a broad range of linear (acenes, phenacenes, biphenylenes, and cyclobuta-acenes) and belt-like (cyclacenes, cyclophenacenes, and cyclobiphenylenes) PAHs containing five to twelve benzene rings. A diverse set of aromaticity descriptors was employed, including geometric (HOMA), electronic (MCI, FLU) and magnetic (NICS) descriptors, plus the recently developed Q2 indices, based on the components of the distributed multipole analysis (DMA) electric quadrupole tensor. These data were complemented by stability analyses using singlet-triplet energy splitting (Delta ES-T) and fractional occupation number-weighted densities (NFOD) values. Our results indicate that acenes and phenacenes follow a comparable aromatic trend, with inner rings possessing lower aromaticity and the edge rings showing a more pronounced aromatic character. A subtle difference is observed in the position of the most aromatic ring, which lies slightly closer to the interior in acenes. Phenacenes, however, exhibit greater overall stability, attributed to their armchair edges. For biphenylenes and cyclobuta-acenes, the antiaromatic cyclobutadiene moiety perturbs the aromaticity only in its direct neighborhood and preserves the aromaticity in the remaining chains. In belt-like systems, cyclacenes exhibit strong radical character and low stability, consistent with longstanding synthetic challenges, whereas cyclophenacenes display enhanced aromaticity and stability with extending size. Cyclobiphenylenes combine localized antiaromatic centers with preserved benzene-like aromaticity in rings distant from the cyclobutadiene unit. (AU) | |
| Processo FAPESP: | 22/16385-8 - Dispositivos orgânicos emissores de luz, conversores de energia via fissão singleto e materiais híbridos 0D/0D para produção de hidrogênio: abordagem da química computacional |
| Beneficiário: | Francisco Bolivar Correto Machado |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |