Síntese, elucidação estrutural e propriedades ópticas de 1,3,2-oxazaborininos diflúor-substituídos

• Ano de defesa: 2023
• Autor(a) principal: Feitosa, Sarah Coelho
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• dARK ID: ark:/26339/001300000bntn
• Idioma: por
• Instituição de defesa: Universidade Federal de Santa Maria; Brasil; Química; UFSM; Programa de Pós-Graduação em Química; Centro de Ciências Naturais e Exatas
• Palavras-chave em Português: β-enamino-α-ceto ésteres; BODIPYs; Complexos diflúor-organoboro; 1,3,2-Oxazaborininos; Propriedades ópticas; β-Enamino-α-keto esters; Difluoro-organoboron complexes; 1,3,2-Oxazaborinines; Optical properties; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
• Link de acesso: http://repositorio.ufsm.br/handle/1/31951

The present work presents the synthesis, spectroscopic structural characterization, microbiological and photophysical properties evaluation of new series of diflúoro-organoboro compounds, BODIPYs analogous, from β-enamino-α-keto ester precursors. Initially, following a methodology already reported in the literature, the synthesis of the (Z)-4-(4-bromophenyl)-4-methoxy-2-oxobut-3-enoate (1) precursor was carried out through the acylation reaction of the acetal derived from 4-bromoacetophenone with ethyloxalyl chloride in the presence of pyridine. Then, the synthesis of a novel series of eight β-aminovinyl-α-keto esters, namely (Z)-4-(arylamino)-4-(4-bromophenyl)-2-oxobut-3-ethyl-enoates (3a-h) was carried out from reaction between ethyl (Z)-4-(4-bromophenyl)-4-methoxy-2-oxobut-3-enoate (1) and different substituted primary arylamines (2a-h) in yields from 63-92%, where aryl = phenyl (a), 4-methoxyphenyl (b), 4-nitrophenyl (c) , 4-bromophenyl(d), 2-naphthyl (e), 2-anthracenyl (f), 9H-fluoren-2-yl (g) e 1-pyrenyl (h). In a subsequent reaction step, these β-enamino-α-keto esters 3 were employed as precursor blocks (NCCCO) in the synthesis of new complexes ethyl 3-aryl-4-(4-bromophenyl)-2,2-diflúoro-2H-1,3λ4,2λ4-oxazaborinino-6-carboxylates (4) in reaction with BF3.OEt2 (BF2 source). Thus, a novel series of eight BF2-complexes could be isolated in 60-80% of yield. The series 3, 4 had their antibacterial activity evaluated with negative results for the microorganism strains Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Streptococcus mutans, Enterococcus faecalis, Klebsiella pneumonie, Proteus mirabilis, Candida albicans) e Chromobacterium violaceum. Lastly, the BF2-complexes 4a-h compounds were also subjected to evaluation of their absorption and emission photophysical properties (UV-Vis). It was found that all the complexes 4 showed no luminescence (emission) in solution, independently of the solvents used in the tests.