Kajiyama Kazuki, Tsurumaki Eiji, Wakamatsu Kan, Fukuhara Gaku, Toyota Shinji
Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.
Department of Chemistry, Faculty of Science, Okayama University of Science, 1-1 Ridaicho, Kita-ku, Okayama, 700-0005, Japan.
Chempluschem. 2021 May;86(5):716-722. doi: 10.1002/cplu.202000816. Epub 2021 Feb 23.
A bicyclic anthracene macrocycle containing two triptycene units at the bridgehead positions was synthesized by Ni-mediated coupling of the corresponding precursor as a cage-shaped aromatic hydrocarbon host. This cage host formed an inclusion complex with C or C guest in 1 : 1 ratio in solution. The association constants (K ) determined by the fluorescence titration method were 1.3×10 and 3.3×10 L mol for the C and C complexes, respectively, at 298 K in toluene. DFT calculations revealed that the guest molecules were included in the middle of the cavity with several CH⋅⋅⋅π contacts. The strong affinity of the cage host for the fullerene guests and the high selectivity toward C are discussed on the basis of spectroscopic and structural data.
通过镍介导的相应前体的偶联反应,合成了一种在桥头位置含有两个三蝶烯单元的双环蒽大环化合物,作为一种笼状芳烃主体。在溶液中,这种笼状主体与C或C客体以1:1的比例形成包合物。在298K的甲苯中,通过荧光滴定法测定的C和C配合物的缔合常数(K)分别为1.3×10和3.3×10 L mol。密度泛函理论计算表明,客体分子通过几个CH⋅⋅⋅π接触被包含在空腔中间。基于光谱和结构数据,讨论了笼状主体对富勒烯客体的强亲和力和对C的高选择性。