| Literature DB >> 30431273 |
Jesús M Fernández-García1, Paul J Evans1, Samara Medina Rivero2, Israel Fernández1, David García-Fresnadillo1, Josefina Perles3, Juan Casado2, Nazario Martín1,4.
Abstract
A geometrically selective bottom-up synthesis of curved nanographenes is described. The synthetic methodology used involves the extension of the π-system of positively curved corannulene by a [4+2] cycloaddition reaction followed by cyclodehydrogenation (Scholl oxidation). By selecting the conditions for the Scholl oxidation, the formation of a seven-membered ring that also confers negative curvature to the resulting nanographene can be activated, offering two topologically distinct, curved nanographenes from a common precursor. Additionally, the structure-property relationship in these new nanographenes is explored via theoretical, electrochemical, photophysical, Raman, and X-ray crystallographic studies.Entities:
Year: 2018 PMID: 30431273 DOI: 10.1021/jacs.8b09992
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419