Kano Haruka, Hayashi Hironobu, Matsuo Kyohei, Fujiki Michiya, Yamada Hiroko, Aratani Naoki
Division of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Division of R&D, True2Materials PTE. Ltd., 8916-5 Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Sci Rep. 2021 Jun 8;11(1):12072. doi: 10.1038/s41598-021-91451-5.
Optically active fullerenes, including C and C derivatives carrying organic substituents, are used in a range of applications because of their unique spectroscopic, catalytic, and chiral recognition properties. However, their inherent photoexcited chirality is yet to be elucidated because of their very poor fluorescence quantum yield (Φ). We synthesised a new chiral C derivative, X70A, with 20% yield, by reacting bis-borylated xanthene with C in a one-step double addition reaction, followed by a successful optical resolution. The isolation of two separate X70A enantiomers was confirmed by mirror-image circular dichroism spectroscopy in the range of 300-750 nm. In toluene, the enantiomeric pair of X70A clearly revealed mirror-image circularly polarised luminescence (CPL) spectra with a high |g| value of 7.0 × 10 at 690 nm. The first fullerene-based deep-red CPL of X70A should provide a new guideline for the design of chiral nanocarbon materials.
包括带有有机取代基的C和C衍生物在内的旋光性富勒烯,因其独特的光谱、催化和手性识别特性而被应用于一系列领域。然而,由于其荧光量子产率(Φ)极低,其固有的光激发手性尚未得到阐明。我们通过双硼酸化呫吨与C在一步双加成反应中反应,然后成功进行光学拆分,以20%的产率合成了一种新的手性C衍生物X70A。通过300 - 750 nm范围内的镜像圆二色光谱证实了两种单独的X70A对映体的分离。在甲苯中,X70A对映体对在690 nm处清晰地显示出镜像圆偏振发光(CPL)光谱,|g|值高达7.0×10。X70A首个基于富勒烯的深红色CPL应为手性纳米碳材料的设计提供新的指导方针。