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

机译:色氨酸手性碳量子点的手性机理研究

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摘要

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.
机译:通过L - / D- -Typtophan(L - / D -TRP)的一步法合成手性,荧光和生物相容性的手性碳量子点(CQDS),作为碳源和手性源。通过透射电子显微镜,傅里叶变换红外光谱法,紫外线可见吸收,激发和发射光谱和圆形二色性(CD)光谱法,表征左旋转移率 - /右旋调节 - CQDS(L - / D -CQDS)。结果表明,L -CQDS和D -CQDS存在类似的球形形态,官能团和光学性质。 CD信号,约220,240和290?nm相反且对称,其结论性地证明L -CQDS和D -CQD是对映体。除了从L - / D -TRP的继承中围绕220nm左右的CD信号,手性环境引起了两个新的手表信号。240和290nm。

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