Cargando…
π-Extended Rubrenes via Dearomative Annulative π-Extension Reaction
[Image: see text] Among a large variety of organic semiconducting materials, rubrene (5,6,11,12-tetraphenyltetracene) represents one of the most prominent molecular entities mainly because of its unusually high carrier mobility. Toward finding superior rubrene-based organic semiconductors, several s...
Autores principales: | Matsuoka, Wataru, Kawahara, Kou P., Ito, Hideto, Sarlah, David, Itami, Kenichiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837837/ https://www.ncbi.nlm.nih.gov/pubmed/36563098 http://dx.doi.org/10.1021/jacs.2c11338 |
Ejemplares similares
-
Diversity-oriented synthesis of nanographenes enabled by dearomative annulative π-extension
por: Matsuoka, Wataru, et al.
Publicado: (2021) -
Annulative π-extension of indoles and pyrroles with diiodobiaryls by Pd catalysis: rapid synthesis of nitrogen-containing polycyclic aromatic compounds
por: Kitano, Hiroyuki, et al.
Publicado: (2018) -
One-shot K-region-selective annulative π-extension for nanographene synthesis and functionalization
por: Ozaki, Kyohei, et al.
Publicado: (2015) -
π-Extension of heterocycles via a Pd-catalyzed heterocyclic aryne annulation: π-extended donors for TADF emitters
por: Spence, Katie A., et al.
Publicado: (2022) -
Synthesis of open-shell ladder π-systems by catalytic C–H annulation of diarylacetylenes
por: Maekawa, Takehisa, et al.
Publicado: (2016)