Piekarski Ashley M, Mills Nancy S, Yousef Abraham
Department of Chemistry, Trinity University, San Antonio, Texas 78212-7200, USA.
J Am Chem Soc. 2008 Nov 5;130(44):14883-90. doi: 10.1021/ja8042323. Epub 2008 Oct 14.
The dianion, 5(2-), and dication, 5(2+), of tetrabenzo[5.7]fulvalene represent an aromaticity/antiaromaticity continuum in which the fluorenyl system changes from aromatic in 5(2-) to antiaromatic in 5(2+). Conversely, the antiaromatic dibenzotropylium system of 5(2-) becomes an aromatic system in 5(2+), allowing an examination of aromaticity/antiaromaticity within the same carbon framework. Dianion 5(2-) was prepared and characterized by (1)H NMR spectroscopy. The fluorenyl system of 5(2-) showed the downfield shifts expected for an aromatic system, while the dibenzotropylium system showed the paratropic shifts expected for an antiaromatic system. The conclusions from (1)H NMR spectroscopy were supported by NICS(1) zz calculations for each system. Comparison of the (1)H NMR spectrum and NICS(1) zz of 5(2-) with those of 5(2+) supported the assignments of aromaticity/antiaromaticity for each system. Aromaticity/antiaromaticity were further examined through comparison of the degree of bond length alternation, which showed that the bond length alternation was slightly greater for the antiaromatic ring systems than for the aromatic systems. However, when structures of 5(2-) and 5(2+) with no bond length alternation were examined, there was a dramatic increase in the degree of antiaromaticity for the antiaromatic ring systems as evaluated through NICS. This result suggests that a decrease in bond length alternation results in an increase in antiaromaticity as well as an increase in aromaticity. The magnitude of the antiaromaticity of the fluorenyl system in 5(2+) was greater than the magnitude of the aromaticity in the fluorenyl system of 5(2-), with similar effects shown by the analogous tropylium systems. This is consistent with the behavior of the antiaromatic dication of tetrabenzo[5.5]fulvalene, compared to that of its aromatic dianion, and also with the behavior of the cyclopentadienyl cation/anion and tropylium cation/anion.
四苯并[5.7]富瓦烯的双负离子5(2-)和双正离子5(2+)代表了一种芳香性/反芳香性连续统,其中芴基体系从5(2-)中的芳香性转变为5(2+)中的反芳香性。相反,5(2-)的反芳香性二苯并环庚三烯体系在5(2+)中变成芳香性体系,从而能够在同一碳骨架内考察芳香性/反芳香性。通过(1)H核磁共振光谱对双负离子5(2-)进行了制备和表征。5(2-)的芴基体系显示出芳香性体系预期的低场位移,而二苯并环庚三烯体系显示出反芳香性体系预期的抗磁环流位移。(1)H核磁共振光谱的结论得到了每个体系的NICS(1) zz计算的支持。将5(2-)的(1)H核磁共振光谱和NICS(1) zz与5(2+)的进行比较,支持了对每个体系芳香性/反芳香性的归属。通过比较键长交替程度进一步考察了芳香性/反芳香性,结果表明,反芳香性环体系的键长交替程度略大于芳香性体系。然而,当考察不存在键长交替的5(2-)和5(2+)的结构时,通过NICS评估,反芳香性环体系的反芳香性程度急剧增加。这一结果表明,键长交替的减少导致反芳香性以及芳香性的增加。5(2+)中芴基体系的反芳香性程度大于5(2-)中芴基体系的芳香性程度,类似的环庚三烯体系也表现出类似的效应。这与四苯并[5.5]富瓦烯的反芳香性双正离子与其芳香性双负离子的行为一致,也与环戊二烯基阳离子/阴离子和环庚三烯基阳离子/阴离子的行为一致。