Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan

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Abstract

Chiral carbon quantum dots (CQDs) with chirality, fluorescence and biocompatibility were synthesized by a one-step method with l-/d-tryptophan (l-/d-Trp), as both carbon source and chiral source. Levogyration-/dextrorotation-CQDs (l-/d-CQDs) were characterized by transmission electron microscopy, Fourier transform infrared spectrometry, ultraviolet-visible absorption, excitation and emission spectrometry and circular dichroism (CD) spectrometry. Results show that l-CQDs and d-CQDs present similar spherical morphology, functional groups and optical properties. The CD signal, around 220, 240 and 290 nm are opposite and symmetric, which conclusively demonstrates that l-CQDs and d-CQDs are enantiomers. Besides the CD signal around 220 nm from the inheritance of l-/d-Trp, two new chiral signals around 240 and 290 nm were induced by chiral environment.

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Wei, Y., Chen, L., Wang, J., Liu, X., Yang, Y., & Yu, S. (2019). Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan. RSC Advances, 9(6), 3208–3214. https://doi.org/10.1039/c8ra09649j

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