Kostyuchenko, Anastasia S. ; Yurpalov, Vyacheslav L. ; Kurowska, Aleksandra ; Domagała, Wojciech ; Proń, Adam ; Fisyuk, Alexander S.
A new synthetic approach towards the preparation of functionalised, soluble, donor–acceptor (DA) alkylbithiophene derivatives of oxadiazole, thiadiazole and triazole is reported. Taking advantage of the Fiesselmann reaction, reactive bithiophene synthons having alkyl or alkoxy substituents at designated positions are prepared. Following a synthetic strategy, featuring the bottom-up approach, sequential structural elements are built, starting from a simple thiophene compound, until the target molecule is obtained, all in good yield. Supplementing the well established methods of oxadiazole and thiadiazole synthesis, efficient ring closure reaction affording a 4H-1,2,4-triazole unit is presented. All target ambipolar compounds display strong photoluminescence with measured quantum yields up to 0.59. Modification of the demonstrated synthetic routes may be exploited for the preparation of longer, specifically functionalised oligothiophenes, coupled to other heteroaromatic cores.
Article is also available on: http://dx.doi.org/10.3762/bjoc.10.165
"Dorobek" bibliographic database - record no. 0000092766 ; oai:repolis.bg.polsl.pl:29899
Oct 1, 2015
Sep 29, 2015
204
https://repolis.bg.polsl.pl/publication/34074
Kurowska, Aleksandra Kostyuchenko, Anastasia S. Zassowski, Paweł Skórka, Łukasz Yurpalov, Vyacheslav L. Fisyuk, Alexander S. Proń, Adam Domagała, Wojciech
Kurowska, Aleksandra Zassowski, Paweł Kostyuchenko, Anastasia S. Zheleznova, Tatyana Yu. Andryukhova, Kseniya V. Fisyuk, Alexander S. Proń, Adam Domagała, Wojciech
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Kurowska, Aleksandra Łapkowski, Mieczysław. Promotor Domagała, Wojciech. Promotor Cabaj, Joanna. Recenzent Kulszewicz-Bajer, Irena. Recenzent
Kurowska, Aleksandra Łapkowski, Mieczysław. Promotor Domagała, Wojciech. Promotor Cabaj, Joanna. Recenzent Kulszewicz-Bajer, Irena. Recenzent
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