氢键
共晶体系
手性(物理)
发光
化学
手性衍生剂
酒石酸
氯化胆碱
乳酸
无机化学
有机化学
手征对称破缺
材料科学
手性柱色谱法
对映体
分子
合金
量子力学
生物
细菌
遗传学
物理
光电子学
Nambu–Jona Lasinio模型
柠檬酸
夸克
作者
Brian P. Nelson,Liam VandenElzen,Grace Whitacre,Todd A. Hopkins
出处
期刊:ChemPhotoChem
[Wiley]
日期:2021-09-07
卷期号:5 (12): 1071-1078
被引量:7
标识
DOI:10.1002/cptc.202100139
摘要
Abstract Deep eutectic solvents (DES) or eutectic mixtures prepared with a chiral component can lead to new chiral solvents with applications that include asymmetric synthesis and chiral light emitting materials. DES have low melting points, because of strong interactions, such as hydrogen bonding, between components of the mixture. Mixtures are prepared with ammonium salts, tetrabutylammonium chloride ([TBA]Cl) and choline chloride ([Ch]Cl), as hydrogen bond acceptor (HBA) and L‐lactic acid, L‐leucic acid, L‐ascorbic acid, R/S‐acetoxypropionic acid, and methyl‐(S)‐lactate as chiral hydrogen bond donors (HBD). Eight combinations of the HBAs and HBDs were prepared, and a racemic mixture of dissymmetric chiral europium complexes was dissolved in the mixtures. The circularly polarized luminescence (CPL) spectra were measured to determine the chiral discrimination by these chiral solvents. The CPL spectra show that the handedness of the chiral HBD is important to the chiral discrimination exhibited. However, the inversion of the sign of the CPL spectra in 1 : 3 [TBA]Cl:L‐lactic acid vs. 1 : 3 [Ch]Cl:L‐lactic acid, and 1 : 1.5 [Ch]Cl:L‐leucic acid vs. 1 : 1 [TBA]Cl:L‐leucic acid shows that the achiral HBA also plays a critical role in the handedness of the chiral discrimination by the chiral solvent.
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