Chiral nanoribbons based on doubly-linked oligo-perylene bisimides
- 23 July 2010
- journal article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 46 (33), 6078-6080
- https://doi.org/10.1039/c0cc01011a
Abstract
A facile strategy towards conformationally stable chiral ladder-type oligo-perylene bisimides is established via copper-mediated Ullmann coupling. Absolute configurations are determined with the help of quantum-chemical calculations.Keywords
This publication has 35 references indexed in Scilit:
- Tetrachloro-tetra(perylene bisimides): an approach towards N-type graphenenanoribbonsChemical Communications, 2010
- Fully Conjugated Tri(perylene bisimides): An Approach to the Construction of n-Type Graphene NanoribbonsJournal of the American Chemical Society, 2008
- Polarized Emission of Individual Self-Assembled Oligo(p-phenylenevinylene)-Based Nanofibers on a Solid SupportJournal of the American Chemical Society, 2005
- Perylene Bisimide Based Macrocycles: Effective Probes for the Assessment of Conformational Effects on Optical PropertiesAngewandte Chemie-International Edition, 2004
- High‐Mobility Air‐Stable n‐Type Semiconductors with Processing Versatility: Dicyanoperylene‐3,4:9,10‐bis(dicarboximides)Angewandte Chemie-International Edition, 2004
- A Pentacene with a 144° TwistJournal of the American Chemical Society, 2004
- Influence of substituents on the rotational energy barrier of atropisomeric biphenyls — studies by polarimetry and dynamic gas chromatographyEuropean Journal of Organic Chemistry, 1995
- Inversionsbarrieren Ortho,ortho′‐verbrückter BiphenyleEuropean Journal of Inorganic Chemistry, 1990
- Enantiomer resolution, absolute configuration, and attempted thermal racemization of two tetrabenzocyclooctatetraene (o-tetraphenylene) derivatives. An exceptionally high barrier to ring inversionThe Journal of Organic Chemistry, 1989
- Ring inversion in di- and tetrabenzocyclootatetraenesJournal of the American Chemical Society, 1972