Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, Denmark.
Chemistry. 2013 Mar 18;19(12):3898-904. doi: 10.1002/chem.201203113. Epub 2013 Feb 10.
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.
氮杂三氧杂[8]轮烯。这是通过用 1,4-苯醌或 1,4-萘醌处理适当官能化的 3,6-二羟基咔唑来实现的。我们通过使用光学、电化学和计算技术以及单晶 X 射线晶体学对氮杂三氧杂[8]轮烯进行了全面表征。计算研究(NICS)的结果表明,当分子处于中性或氧化态(2+)时,中心平面环辛四烯是反芳香的,相应的二阴离子是芳香的。我们讨论了平面环辛四烯的芳香/反芳香性质,并将其与等电子的四氧杂[8]轮烯进行了比较。