Fujimura Koki, Ueda Yoshihiro, Yamaoka Yousuke, Takasu Kiyosei, Kawabata Takeo
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Current address: Interdisciplinary Research Center for Catalytic Chemistry, National Institute of Advanced Industrial Science and Technology, Tsukuba Central 5-2, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8565, Japan.
Angew Chem Int Ed Engl. 2023 Jul 24;62(30):e202303078. doi: 10.1002/anie.202303078. Epub 2023 Jun 20.
A method for rotaxane synthesis by enlargement of the size of the terminal phenol group of the axle component by aromatic bromination has been developed. This method may be regarded as an end-capping strategy involving the swelling of the phenol group at the axle terminal. The advantages of the present strategy include: ready availability of axle components with a variety of swelling precursors, wide product scope (19 examples given including a [3]rotaxane), mild conditions for the swelling process, rich potential for the derivatization of the brominated rotaxanes, and possible release of the axle component by degradative dethreading of the thermally stable brominated rotaxanes under the basic conditions.
已开发出一种通过芳基溴化增大轴组件末端酚基团大小来合成轮烷的方法。该方法可被视为一种封端策略,涉及轴末端酚基团的膨胀。本策略的优点包括:可方便地获得带有各种膨胀前体的轴组件,产品范围广(给出了19个例子,包括一个[3]轮烷),膨胀过程条件温和,溴化轮烷的衍生化潜力大,以及在碱性条件下热稳定的溴化轮烷可通过降解脱线释放轴组件。