On the recognition of chloride, bromide and nitrate anions by anthracene-squaramide conjugated compounds: a computational perspective

Autor(es)

Orenha, Renato Pereira ; da Silva, Vanessa Borges ; Caramori, Giovanni Finoto ; de Souza Schneider, Felipe Silveira ; Piotrowski, Mauricio Jeomar ; Contreras-Garcia, Julia ; Cardenas, Carlos ; Briese Goncalves, Marina ; Mendizabal, Fernando ; Parreira, Renato Luis Tame

• Tipo de documento: Artigo Científico
• Fonte: NEW JOURNAL OF CHEMISTRY; v. 44, n. 41, p. 9-pg., 2020-11-07.

Resumo

Anion recognition is widely used in several biological fields. Squaramide derived compounds appear as potential structures to recognize anions. Here, the bond mechanisms between the chloride (Cl-), bromide (Br-) and nitrate (NO3-) anions and anthracene-squaramide conjugated compounds are elucidated considering the influence of the: (i) number, (ii) nature, and (iii) position of the substituents: trifluoromethyl (-CF3) and nitro (-NO2). Energy decomposition analysis (EDA) shows that the interactions between Cl-, Br- and NO3- and anthracene-squaramide have an attractive interaction energy supported predominantly by electrostatic energy followed by orbital contribution. Molecular electrostatic potential (MEP) surfaces imply electrostatic interactions between Cl-, Br- and the oxygen atom from NO3- and the hydrogen atoms from N-H and C-H bonds present in the squaramide structure, and an aryl group, respectively. Cl- interacts with the receptors more strongly than Br-. The NO3- recognition is less attractive than those presented by Cl- and Br-, in agreement with the hardness-softness features of these anions. Importantly, one and, mostly, two group substitutions, -H -> -CF3 or -NO2, favor the recognition of Cl-, Br- and NO3- due to the increase of the polarization in the receptor-NHMIDLINE HORIZONTAL ELLIPSISanion interaction. The -NO2 group promotes a larger effect relative to the -CF3 ligand. The -NO2 ligand positioned at the largest distance conceivable to the benzene-NH group promotes the lowest interference in the N-HMIDLINE HORIZONTAL ELLIPSISCl- interaction. These results provide information to design receptors with a larger capability to recognize anions. (AU)

• Processo FAPESP: 19/19175-1 - 5a Escola de Química Computacional - "Modelagem em Química Supramolecular"
• Beneficiário: Renato Luis Tame Parreira
• Modalidade de apoio: Auxílio Organização - Reunião Científica
• Processo FAPESP: 11/07623-8 - Utilização de métodos mecânicos-quânticos para estudo das ligações e interações químicas em sistemas auto-organizados com aplicação em catálise, química medicinal, eletrocromismo, armazenamento e conversão de energia
• Beneficiário: Renato Luis Tame Parreira
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores
• Processo FAPESP: 17/24856-2 - O Mecanismo da Reação de Substituição do Ligante Nitrosil por Aqua em Compostos de Coordenação de Rutênio
• Beneficiário: Renato Pereira Orenha
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado