| Literature DB >> 28771920 |
Justus Krüger1, Fátima García2, Frank Eisenhut1, Dmitry Skidin1, José M Alonso2, Enrique Guitián2, Dolores Pérez2, Gianaurelio Cuniberti1, Francesca Moresco1, Diego Peña2.
Abstract
Acenes are intriguing molecules with unique electronic properties. The difficulties in their preparation owing to low stability under ambient conditions are apparent because successful syntheses of long unsubstituted acenes are still scarce, in spite of the great attention they have attracted. Only unsubstituted acenes up to heptacene have been isolated in bulk, with nonacene being the largest acene detected to date. Herein we use on-surface assisted reduction of tetraepoxy decacene precursors on Au(111) as the key step to generate unprecedented decacene which is visualized and its electronic resonances studied by scanning tunneling microscopy (STM) and spectroscopy (STS).Entities:
Keywords: acenes; decacene; deoxygenation; molecular resonance imaging; on-surface chemistry
Year: 2017 PMID: 28771920 DOI: 10.1002/anie.201706156
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336