Utilize este identificador para referenciar este registo:
https://hdl.handle.net/1822/49500
Título: | Synthesis and characterization of four novel 1,3-azole based push-pull heterocyclic systems |
Autor(es): | Raposo, M. Manuela M. Fernandes, Sara Sofia Marques |
Palavras-chave: | Synthesis Benzothiazole benzimidazole Benzoxazole Thiophene Pyrrole Push-pull heterocyclcic systems UV-vis spectroscopy Fluorescence |
Data: | 2017 |
Citação: | Fernandes, S. S. M.; Raposo, M. M. M. Synthesis and characterization of four novel 1,3-azole based push-pull heterocyclic systems. 21st Int. Electron. Conf. Synth. Org. Chem., 1–30 November 2017; Sciforum Electronic Conference Series, 2017, Vol. 21. |
Resumo(s): | Four novel 1-(4-thiophene-2-yl)phenyl)-1H-pyrrole derivatives functionalized with different 1,3-azole moieties fused with a phenyl ring have been synthesized, in fair yields, and their optical properties studied. The results showed that the optical properties could be readily tuned by changing the electronic nature of the azole ring, or even with the introduction of a nitro group. The benzothiazole, benzimidazole and benzoxazole heterocycles are heteroaromatic electron deficient moieties that act as both acceptor groups and -conjugated spacers with auxiliary electron withdrawing ability.1 Moreover, benzimidazole derivatives offers the possibility of substitution on the nitrogen atom for further tuning of their optical and electronic properties. Benz[X]azole derivatives are interesting compounds with several optical applications,2 and as biologically active compounds.3 |
Tipo: | Resumo em ata de conferência |
URI: | https://hdl.handle.net/1822/49500 |
Versão da editora: | http://sciforum.net/conference/ecsoc-21/paper/4789 |
Arbitragem científica: | yes |
Acesso: | Acesso aberto |
Aparece nas coleções: | CDQuim - Comunicações e Proceedings |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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Communication ECSOC 17- doi 10.3390-ecsoc-21-04789.pdf | Communication ECSOC 17- doi 10.3390-ecsoc-21-04789 | 253,11 kB | Adobe PDF | Ver/Abrir |
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