Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/50721

TitleSynthesis and characterization of novel thienylpyridazine derivatives
Author(s)Fernandes, S. S. M.
Raposo, M. Manuela M.
KeywordsSynthesis
Pyridazines
Pyrrole
Thiophene
diazines
heterocycles
Push-pull π-conjugated heterocyclic compounds
Optical applications
Suzuki cross-coupling
UV-vis spectroscopy
Issue date2015
PublisherMDPI
CitationFernandes, S. S. M.; Raposo, M. M. M. Synthesis and characterization of novel thienylpyridazine derivatives. Proceedings of the 18th Int. Electron. Conf. Synth. Org. Chem., a016; Sciforum Electronic Conference Series, Vol. 18; Seijas, J. A.; Tato, M. P. V. and Lin, S.-K. (Eds), MDPI, Basel, Switzerland, 2015 (ISBN: 978-3-906980-55-3).
Abstract(s)Recently, the exploration of thiophene π-conjugated systems functionalized with donor-acceptor groups has greatly expanded due to the increased interest in optoelectronic, photovoltaic and OLED applications. This type of molecules are highly targeted due to the easy tuning of the photophysical properties by small structural modifications 1-7. A few thienylpyridazines were synthesized as part of an on-going research directed to the development of donor-acceptor substituted heterocyclic systems for several optical (linear and nonlinear)8-9 and DSSCs applications. In this communication we report the synthesis and the photophysical characterization of novel thienylpyridazine derivatives, functionalized in position 3, with different donor groups (thiophene, pyrrole and N,N-dialkylphenylamine). The diazines were synthesized by Suzuki coupling of 3-bromo-6-(thiophen-2-yl)pyridazine with commercially available (hetero)aryl-boronic acids. On the other hand, precursor 3-bromo-6-(thiophen-2-yl)pyridazine was prepared by reaction of a thienylpyridazinone with POBr3 10.
TypeConference paper
URIhttp://hdl.handle.net/1822/50721
ISBN978-3-906980-55-3
DOI10.3390/ecsoc-18-a016
Publisher versionhttp://dx.doi.org/10.3390/ecsoc-18-a016
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDQuim - Comunicações e Proceedings

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