Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamada-oka, Suita, Osaka 565-0871, Japan.
Chem Commun (Camb). 2011 Oct 14;47(38):10524-35. doi: 10.1039/c1cc12532j. Epub 2011 Jul 8.
Nonplanar polyaromatic carbon molecules including fullerenes and carbon nanotubes have been attracting great interest due to their potential as materials, catalysts, etc. In this context, bowl-shaped polyaromatic hydrocarbons (π bowls) are considered to be key materials in the science of nonplanar π-conjugated carbon systems. Among π bowls, we focused on a molecular bowl "sumanene (C(21)H(12))" featuring a C(3v) symmetric structural motif present in fullerenes or carbon nanotube molecules. In this article, we present the research on sumanenes to date, including their synthesis, structural characterization, derivatization, complexation, and their potential uses as electrical materials. The characteristic structural feature of a sumanene depends on three sp(3) hybridized carbon atoms at the benzylic positions. Facile functionalization via selective formation of benzylic anions gives stereoselective substituted compounds, the π-extended derivatives, and the deeper π bowls. Furthermore, the dynamically flexible aspect based on bowl-to-bowl inversion is also described. The crystal with a columnar bowl-in-bowl stacking exhibits a high electron transport ability with anisotropy. Complexation with a cyclopentadienyl iron cation results in the first selective formation of the concave-bound complex as a π-bowl complex.
非平面多环芳烃分子,包括富勒烯和碳纳米管,由于它们作为材料、催化剂等的潜力而引起了极大的兴趣。在这种情况下,碗状多环芳烃(π碗)被认为是非平面π共轭碳体系科学中的关键材料。在π碗中,我们关注的是一种分子碗“sumanene(C(21)H(12))”,它具有富勒烯或碳纳米管分子中存在的 C(3v)对称结构基序。在本文中,我们介绍了迄今为止对 sumanene 的研究,包括它们的合成、结构表征、衍生化、络合以及作为电材料的潜在用途。sumanene 的特征结构特征取决于苄位的三个 sp(3)杂化碳原子。通过选择性形成苄基阴离子进行的简便官能化给出了立体选择性取代化合物、π扩展衍生物和更深的 π 碗。此外,还描述了基于碗到碗反转的动态灵活方面。具有柱状碗对碗堆积的晶体表现出具有各向异性的高电子传输能力。与环戊二烯基铁阳离子的络合导致作为 π 碗络合物的第一个凹面结合络合物的选择性形成。