期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 72, 期 26, 页码 10096-10107出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo701939c
关键词
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The dications 6, 7, and 8 and dianions 9, 10, and 11 of the bistricyclic aromatic enes bifluorenylidene (1), 1,1'-biphenalenylidene (2), and 9-(9H-fluoren-9-ylidene)-1H-phenalene (4), as well as monocations 12a and 13a and monoanions 14a and 15a of phenalene (3) and, fluorene (5), were subjected to a systematic DFT and ab initio study. B3LYP and MP2 methods were employed to estimate the relative aromaticity/antiaromaticity of these ions, using energetic, magnetic, and structural criteria. The couplings of monoions 12a-15a to give the respective diions 6-11 result in a similar destabilization in both the fluorene and phenalene series. The interactions between the C13H8 units in diions 6-11 are weak and are not expected to result in a significant loss of aromaticity/gain of antiaromaticity, as compared with the respective monoions. The antiaromaticity of bifluorenylidene dication (6), relative to that of two fluorenyl cations (12a), is only slightly enhanced as compared with the aromaticity of biphenalenylidene dication ((E)-7)) relative to that of two phenalenyl cations (13a). In particular, the homodesmotic reaction 6 + 2 center dot 13a = (E)-7 + 2 center dot 12a is only slightly exothermic, Delta E-Tot = -6.0 kJ/mol. The energetic effect of the analogous reaction involving anions 9 + 2 center dot 15a = (E)-10 + 2 center dot 14a is even smaller, Delta E-Tot = -3.4 kJ/mol. Bifluorenylidene dianion (9) and 1,1'-biphenalenylidene dianion ((E)-10) are aromatic, but the employed criteria disagree about their relative aromaticity. The electronic and structural properties of heteromerous dication 8 and dianion 11 lie between those of the homomerous diions. Thus, dications 6-8 and dianions 9-11 form a continuum of aromaticitylantiaromaticity.
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