对映体
发光
超分子化学
对映体过量
材料科学
离子
结晶学
配体(生物化学)
分子
立体化学
化学
晶体结构
对映选择合成
有机化学
光电子学
催化作用
受体
生物化学
作者
Wenwen Li,Yanyan Zhou,Ting Gao,Jingya Li,Sen Yin,Wenru Huang,Yuying Li,Qing Ma,Zhiwei Yao,Peng‐Fei Yan,Hongfeng Li
标识
DOI:10.1021/acsami.2c17967
摘要
Undoubtably, it is challenging to simultaneously determine the identity, enantiomeric excess (ee), and total concentration of an enantiomer by just one optical measurement. Herein, we design a chiral tetrahedron Eu4(LR)4 with circularly polarized luminescence (CPL), which presents highly selective/stereoselective, rapid, and "turn-on" CPL response to chiral diamines, rather than the monoamino compounds, such as monoamines or amino alcohols. By recording the left- and right-CPL intensities of the Eu3+ ion at 591 nm, the enantiomeric composition and concentration of chiral diamines can be simultaneously determined by monitoring the glum value and total emission intensity (IL + IR), respectively. Spectroscopy analyses demonstrate that the variations of glum depend on the inversion and maintenance of configuration around the Eu3+ ion (Δ ↔ Λ), while the "turn-on" response arises from the raising of the T1 state of the ligand. The molecule/electron structural variations are proposed from the synergetic supramolecular interactions of NH2 groups with pendant diols and trifluoroacetyl groups.
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