Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Mikhail Feofanov"'
Autor:
Dominik Lungerich, Olena Papaianina, Mikhail Feofanov, Jia Liu, Mirunalini Devarajulu, Sergey I. Troyanov, Sabine Maier, Konstantin Amsharov
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-8 (2018)
Nanographenes with zig-zag peripheries are expected to have unique electronic properties, but their application in organic electronics has been curbed by their difficult synthesis. Here, the authors develop a facile route to zig-zag nanographenes bas
Externí odkaz:
https://doaj.org/article/6971a8726b954defa992d140ec38872c
Publikováno v:
Chemistry – A European Journal. 27:17322-17325
Herein, we report a new method for synthesis of extended perylenes and terrylenes. The technique is based on the cascade dehydrative π-extensions (DPEX) of aryl aldehydes, in which stepwise annulations activate previously "dormant" substituents. Two
Publikováno v:
ChemistrySelect. 6:10671-10673
Publikováno v:
Angewandte Chemie (International Ed. in English)
A novel catalyst‐free approach to benzoannulated oxygen‐containing heterocycles from fluorinated oligophenylenes is reported. Unlike existing methods, the presented reaction does not require an oxygen‐containing precursor and relies on an exter
Publikováno v:
Chemical Communications. 57:12325-12328
Caryl–F bond activation has become an important and quickly developing method for construction of carbon-based materials. We report that alumina-mediated C–F bond activation (AmCFA) enables construction of PAHs with zigzag periphery. This method
Autor:
Vladimir Akhmetov, Mikhail Feofanov, Cordula Ruppenstein, Josefine Lange, Dmitry Sharapa, Marjan Krstić, Frank Hampel, Evgeny A. Kataev, Konstantin Amsharov
Publikováno v:
Chemistry – A European Journal. 28
Autor:
Dominik Lungerich, Marcus Halik, Konstantin Amsharov, Marco Sarcletti, Judith E. Wittmann, Mikhail Feofanov, Baolin Zhao, Tobias Rejek, Hyoungwon Park
Publikováno v:
Frontiers of Materials Science. 14:314-322
Polycyclic aromatic hydrocarbons with zigzag peripheries are high perspective candidates for organic electronics. However, large fused acenes are still poorly studied due to the tedious synthesis. Herein we report a non-substituted fused bistetracene
Publikováno v:
Photochemical & Photobiological Sciences. 19:722-725
The synthesis of ten ortho-fused PAHs bearing boronic pinacol ester groups (BPin) is reported. The products are obtained via modification of Mallory photocyclization in 45–99% yields. Among them are examples of highly strained molecules such as [4]
Autor:
Mikhail Feofanov, Andreas Förtsch, Vladimir Akhmetov, Konstantin Amsharov, Sergey I. Troyanov
Publikováno v:
Organic Chemistry Frontiers. 7:1271-1275
An unprecedented [6]helicene's cavity closure indicating the possibility of introducing seven-membered rings via alumina-mediated C–F activation is shown. This finding, in combination with a directed quadruple annulation of fluorinated oligoarylene
Publikováno v:
Chemical Communications. 56:14377-14380
Herein we report a transition-metal free activation of a particularly stable aromatic carbon–fluorine bond allowing intramolecular aryl–aryl coupling which is orthogonal to carbon–iodine functionality.