手性(物理)
发光
圆极化
反演(地质)
配体(生物化学)
立体化学
化学
材料科学
结晶学
物理
光学
生物化学
光电子学
生物
手征微扰理论
受体
量子力学
古生物学
π介子
构造盆地
Nambu–Jona Lasinio模型
微带线
作者
Hong‐Ru Fu,Dan‐Dan Ren,Kun Zhang,Ruoyu Zhang,Xiaoyan Lu,Ya‐Pan Wu,Francisco Aznárez,Qing-Rong Ding,Lu‐Fang Ma,Dong‐Sheng Li
标识
DOI:10.1021/acsmaterialslett.4c00619
摘要
Chirality inversion modulation is of great importance in the preparation of chiroptical materials. The rational use of the stoichiometry of mixed ligands in chiral metal–organic frameworks (MOFs) to induce chiral inversion of the enantiomeric space groups is a crucial topic in structural chemistry. However, no remarkable results have been reported yet. In this work, we synthesized chiral MOFs through the assembly of chiral camphoric acid ( d / l -cam) and achiral tetradentate ligands. Interestingly, the visible single-crystal structures confirmed that chirality inversion of the enantiomeric space groups can be achieved via stoichiometric modulation of mixed ligands. Significantly, the switches of circularly polarized luminescence (CPL) along with the inversion of enantiomeric space groups can be observed clearly. Moreover, the encapsulated guest emitters exhibit the inverted CPL, revealing the helical-channel-dependent chirality transfer. The obtained results constitute a milestone in the field of chiral crystal engineering of MOFs.
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