圆二色性
发光
对映体
不对称碳
质子化
手性(物理)
结晶学
化学
发色团
光化学
超分子手性
脱质子化
材料科学
线性二色性
立体化学
共价键
圆极化
组氨酸
配体(生物化学)
咪唑
磁圆二色性
作者
Lin Cai,Jiancheng Liu,Jiayi Liu,Zhongzheng Guo,Yulu He,Yatao Pan,Xia Ran,Renming Liu,Lijun Guo,Songnan Qu
摘要
Carbon dots (CDs) have garnered significant attention for developing stimuli-responsive chiroptical nanomaterials. However, CDs featuring simultaneously reversible electronic circular dichroism (ECD) and intrinsic circularly polarized luminescence (CPL) have not yet been reported. Herein, we developed a novel kind of dual-mode chiroptical switches based on achiral CDs through post-modification with L-/D-histidine (L-/D-His). Through a mild amidation reaction, L-/D-His is not only covalently linked to the surface of CDs, but also closely attached to the luminescent centers via non-covalent hydrogen-bonding and π-π interactions, which facilitate efficient chiral transfer from L-/D-His to the luminescent centers of the CDs. Consequently, the chiral His-modified achiral CDs (L-/D-His-CDs) exhibit attractive chiroptical properties with both elegant ECD and intrinsic CPL across the entire visible spectrum. Intriguingly, the ECD and CPL signals of L-/D-His-CDs can be reversibly switched to those of their enantiomers by alternating pH values between neutral and basic conditions. Our results indicate that the pH-modulated protonation and deprotonation of imidazole directly modulate the surface non-covalent interactions, triggering chiral conformational inversion and thereby enabling reversible ECD and CPL signals. This study establishes a facile strategy for the construction of stimuli-responsive chiroptical switches from achiral CDs by rational chiral ligand modifications.
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