| Literature DB >> 29115021 |
Robert G Clevenger1, Bharat Kumar2, Elizabeth M Menuey1, Gene-Hsiang Lee3, Dustin Patterson2, Kathleen V Kilway1.
Abstract
Seven longitudinally twisted acenes (an anthracene, two tetracenes, three pentacenes, and a hexacene) have been synthesized by the addition of aryllithium reagents to the appropriate quinone precursors, followed by SnCl2 -mediated reduction of their diol intermediates, and several of these acenes have been crystallographically characterized. The new syntheses of the three previously reported twisted acenes, decaphenylanthracene (1), 9,10,11,20,21,22-hexaphenyltetrabenzo[a,c,l,n]pentacene (2), and 9,10,11,12,13,14,15,16-octaphenyldibenzo[a,c]tetracene (14), resulted in a reduction of the number of synthetic steps. As a consequence their overall yields were increased by factors of 50-, 24-, and 66-fold, respectively. All of the twisted acene syntheses reported here are suitable for the synthesis of at least gram quantities of these remarkable hydrocarbon materials.Entities:
Keywords: acenes; pentacene; quinones; reduction; tetracene
Year: 2017 PMID: 29115021 DOI: 10.1002/chem.201704501
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236