Kuwatani Yoshiyuki, Yamamoto Gaku, Iyoda Masahiko
Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan.
Org Lett. 2003 Sep 18;5(19):3371-4. doi: 10.1021/ol030055g.
[reaction: see text] Three extended [4]radialenes with two tricyclic rings connected with exocyclic butatriene units have been synthesized. The compounds, possessing thioxanthene and dihydroanthracene moieties as the terminal substituents, show a fast rotation around the butatriene bonds at ambient temperatures (DeltaG() = 13.7 and 14.9 kcal/mol, respectively). In contrast, the fluorene-substituted analogue shows a much higher rotational barrier (DeltaG() = 17.8 kcal/mol) of the butatriene bonds due to the reduced steric repulsion between the two fluorene moieties at the ground state.
[反应:见正文] 已合成了三种带有两个通过环外丁三烯单元相连的三环的扩展[4]轮烯。这些化合物以噻吨和二氢蒽部分作为末端取代基,在环境温度下围绕丁三烯键表现出快速旋转(ΔG‡分别为13.7和14.9千卡/摩尔)。相比之下,芴取代的类似物由于基态下两个芴部分之间的空间排斥减小,丁三烯键的旋转势垒要高得多(ΔG‡ = 17.8千卡/摩尔)。