对映体药物
对映体
手性拆分
化学
分辨率(逻辑)
结晶
对映体过量
诱导剂
乳酸
绝对构型
立体化学
对映选择合成
有机化学
催化作用
计算机科学
生物
基因
人工智能
生物化学
遗传学
细菌
作者
Man-Ting Chen,Zuo‐Chang Chen,Huijun Chen,Li Xu,Xiang‐Jian Kong,Long Liu,Lan‐Sun Zheng
标识
DOI:10.1007/s11426-021-1065-9
摘要
The asymmetric assembly and spontaneous resolution of chiral heterometal-organic frameworks from achiral precursors remain a great challenge. Herein, we report the formation and spontaneous resolution of three-dimensional (3D) chiral 3d–4f heterometal-organic frameworks from achiral ligands in the presence of lactic acid enantiomers as chiral inducers. In the absence of a chiral inducer, the reactants randomly generated both enantiopure crystals in equal measure. However, enantiopure lactic acid induced asymmetric resolution to achieve single chiral crystallization. DFT theoretical calculations showed that the absolute chiral resolution of the enantiomers is due to the difference in the interactions between the two enantiomeric Λ/Δ-[FeL3]3− units and the chiral inducer.
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