| Texto completo | |
| Autor(es): |
Santos, Jose L. F.
;
de Souza, Gabriel L. C.
Número total de Autores: 2
|
| Tipo de documento: | Artigo Científico |
| Fonte: | COMPUTATIONAL AND THEORETICAL CHEMISTRY; v. 1256, p. 8-pg., 2026-02-01. |
| Resumo | |
We performed a computational study of the ground state and five lowest excited singlet states of oxygenated polycyclic aromatic hydrocarbons (O-PAHs) derived from phenanthroline: 9,10-phenanthrenequinone, 4,7-phenanthroline-5,6-dione, and 1,10-phenanthroline-5,6-dione. Ground-and excited-state properties were determined using density functional theory (DFT) and time-dependent DFT, respectively, at the CAM-B3LYP/cc-pVTZ level of theory, in both gas phase and aqueous solution. Solvation was modeled through the polarizable continuum model (PCM) and a composite solvation model (CSM) combining explicit water molecules with PCM. Microsolvation stabilized preferential interactions at nitrogen sites and caused the emergence of a bright state in 9,10-phenanthrenequinone, absent in the gas phase. In contrast, 4,7-phenanthroline-5,6-dione and 1,10-phenanthroline-5,6-dione showed no bright states. These findings suggest that the combined presence of a diketone group and nitrogen heteroatoms may exert a significant influence on the photoabsorption process, thereby hindering the photodecomposition of O-PAHs in both the gas phase and aqueous solution, relative to the corresponding polycyclic aromatic hydrocarbons (PAHs) and nitrogen-containing PAHs (N-PAHs). (AU) | |
| Processo FAPESP: | 23/11043-4 - Ionização de Agregados Moleculares de Relevância Biológica |
| Beneficiário: | Gabriel Luiz Cruz de Souza |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |