Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/48516

TitleSynthesis and characterization of four novel 1,3-azole based push-pull heterocyclic systems.
Author(s)Fernandes, S. S. M.
Raposo, M. Manuela M.
Keywordsbenz[X]azole
thiophene
pyrrole
push-pull heterocyclic systems
synthesis
nonlinear optics (NLO)
UV-visible
fluorescence
Issue dateNov-2017
PublisherSciforum Electronic Conferences Series
CitationFernandes, S. S. M.; Raposo, M. M. M. Synthesis and characterization of four novel 1,3-azole based push-pull heterocyclic systems. Proceedings of the 21st Int. Electron. Conf. Synth. Org. Chem., 1–30 November 2017; Sciforum Electronic Conference Series, 2017, Vol. 21; doi:10.3390/ecsoc-21-04789. http://sciforum.net/conference/ecsoc-21/paper/4789
Abstract(s)Benz[X]azole derivatives are interesting compounds due to their diverse biological activities and interesting optical properties. The benzothiazole, benzimidazole and benzoxazole heterocycles are heteroaromatic electron deficient moieties that act as both acceptor groups and π-conjugated spacers with auxiliary electron withdrawing ability. Moreover, benzimidazole derivatives offers the possibility of substitution on the nitrogen atom for further tuning of their optical and electronic properties. Recently we have reported the synthesis and evaluation of the electronic, thermal and optical properties of a large number of series of benz[X]azole derivatives functionalized with different π-spacers having in mind their application as optical chemosensors, nonlinear optical and photochromic materials, and emissive organic components for OLEDs. In continuation of the work developed in our research group, we report in this work the synthesis, the characterization and the evaluation of the optical properties of four novel 1-(4thiophene-2-yl)phenyl)-1H-pyrrole derivatives functionalized with different benz[X]azole moieties (benzothiazole, benzimidazole and benzoxazole). The results showed that the optical properties could be readily tuned by changing the electronic nature of the azole ring, or even by introduction of a strong acceptor group.
TypeConference paper
URIhttp://hdl.handle.net/1822/48516
DOI10.3390/ecsoc-21-04789
Publisher versionhttp://sciforum.net/conference/ecsoc-21/paper/4789
Peer-Reviewedyes
AccessEmbargoed access (2 Years)
Appears in Collections:CDQuim - Comunicações e Proceedings

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