| Literature DB >> 30474286 |
Narcisse Ukwitegetse1, Patrick J G Saris1, Jonathan R Sommer1, Ralf M Haiges1, Peter I Djurovich1, Mark E Thompson1.
Abstract
Tetra-aza-pentacenes are attractive n-type small molecules for optoelectronic device applications, yet their syntheses are often laborious. Disclosed here is a one-pot Friedländer synthesis of 1,7,8,14-tetraazapentacece (tAP) derivatives (linear and/or bent), fully aromatized in situ despite the absence of an exogenous oxidant. The photophysics of linear tAPs resembles that of regular pentacene though their crystal structures differ. A LUMO energy of -3.71 eV for di-tert-butylanisole-substituted linear tAP is similar to that of the well-known acceptor, C60 .Entities:
Keywords: Friedländer reaction; acenes; n-type molecules; one-pot synthesis; tetra-aza-pentacene
Year: 2018 PMID: 30474286 DOI: 10.1002/chem.201805655
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236