| Literature DB >> 23400907 |
Christian B Nielsen1, Theis Brock-Nannestad, Peter Hammershøj, Theis K Reenberg, Magnus Schau-Magnussen, Denis Trpcevski, Thomas Hensel, Roberto Salcedo, Gleb V Baryshnikov, Boris F Minaev, Michael Pittelkow.
Abstract
We describe herein the first synthesis of a new class of anti-aromatic planar cyclooctatetraenes: the azatrioxa[8]circulenes. This was achieved by treating a suitably functionalised 3,6-dihydroxycarbazole with 1,4-benzoquinones or a 1,4-naphthoquinone. We fully characterised the azatrioxa[8]circulenes by using optical, electrochemical and computational techniques as well as by single-crystal X-ray crystallography. The results of a computational study (NICS) suggest that the central planar cyclooctatetraene is anti-aromatic when the molecules are in neutral or oxidised states (2+), and that the corresponding dianions are aromatic. We discuss the aromatic/anti-aromatic nature of the planar cyclooctatetraenes and compare them with the isoelectronic tetraoxa[8]circulenes.Entities:
Year: 2013 PMID: 23400907 DOI: 10.1002/chem.201203113
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236