对映体
催化作用
色氨酸
异构化
羟醛缩合
不对称碳
化学
碳纤维
羟醛反应
手性(物理)
对映体过量
组合化学
光化学
对映选择合成
有机化学
材料科学
氨基酸
光学活性
手征对称破缺
生物化学
复合数
复合材料
物理
量子力学
Nambu–Jona Lasinio模型
夸克
作者
Mengling Zhang,Xing Fan,Xin Du,Yurong Ma,Xiting Wang,Hui Huang,Yang Liu,Youyong Li,Zhenhui Kang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-04-18
卷期号:16 (7): 8929-8936
被引量:12
标识
DOI:10.1007/s12274-023-5601-6
摘要
Chiral catalysis is one of the most direct and effective approach to obtain pure optical enantiomers. Chiral carbon dots (CDs) as carbon-based chiral catalysts show great potential in chiral catalysis. Herein, we report a facile one step base-catalyzed aldol condensation to fabricate the chiral CDs from glucose at ambient temperature and pressure. The formation of chiral CDs involves the processes of isomerization and aldol condensation. These chiral CDs have been demonstrated that they have selective capacity for electrocatalytic oxidization of tryptophan enantiomers. L type of CDs (LCDs) is more likely to catalyze L-tryptophan (Trp) than D-Trp with the selective factor (/L//D) of 1.60, whereas the D type of CDs (DCDs) tends to catalyze D-Trp (/L//D: 0.63). Theoretical calculations combined with various contrast experiments (temperature and pH) demonstrate that the selectively electrocatalytic capacity of chiral CDs toward Trp isomers is due to the different hydrogen-bond interactions between chiral CDs and Trp.
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