手性(物理)
对映体
纳米材料
色氨酸
量子点
超分子手性
荧光
超分子化学
对映选择合成
化学
纳米技术
光化学
物理
材料科学
分子
立体化学
有机化学
手征对称破缺
催化作用
生物化学
量子力学
氨基酸
Nambu–Jona Lasinio模型
夸克
作者
Nafiseh Fahimi-Kashani,Zahra Jafar-Nezhad Ivrigh,Arafeh Bigdeli,Mohammad Reza Hormozi-Nezhad
标识
DOI:10.1021/acsanm.1c02928
摘要
Discrimination of chiral targets is generally achieved with chiral nanomaterials. However, the limited number of intrinsic chiral nanostructures as well as their complex synthesis procedure has led to the production of chirality-induced nanomaterials as alternatives. Chirality can be induced in nanomaterials by either chirality transfer or the formation of chiral assemblies. Using the latter approach, in this work, we have provided chiral supramolecular assemblies of CdTe quantum dots (QDs) from achiral starting materials. CTAB-QD assemblies showed chiroptical activities, and their orange emission in combination with the blue emission of carbon dots was utilized as a ratiometric chiral recognition platform for enantioselective detection of tryptophan (Trp). Entirely distinct fluorescence response patterns were obtained in the presence of L- and D-Trp. While D-Trp suppressed the fluorescence emission of CTAB-QDs, which was also accompanied by a substantial alteration in the emission color from peach to purple, only slight spectral changes were observed in the presence of L-Trp. The distinct response patterns of the ratiometric assay were further manipulated for the construction of a logic gate system mimicking NOT and OR functions. The applicability of the supramolecular chiral assembly toward enantiomeric excess determination of L-Trp in food supplements was also investigated. The acquired wide range color tonalities enable simple visual tracking of D- and L-Trp with a handheld device such as a smartphone.
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