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

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, Fo...

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Autores principales: Wei, Yingying, Chen, Lin, Wang, Junli, Liu, Xuguang, Yang, Yongzhen, Yu, Shiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059925/
https://www.ncbi.nlm.nih.gov/pubmed/35518943
http://dx.doi.org/10.1039/c8ra09649j
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author Wei, Yingying
Chen, Lin
Wang, Junli
Liu, Xuguang
Yang, Yongzhen
Yu, Shiping
author_facet Wei, Yingying
Chen, Lin
Wang, Junli
Liu, Xuguang
Yang, Yongzhen
Yu, Shiping
author_sort Wei, Yingying
collection PubMed
description 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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spelling pubmed-90599252022-05-04 Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan Wei, Yingying Chen, Lin Wang, Junli Liu, Xuguang Yang, Yongzhen Yu, Shiping RSC Adv Chemistry 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. The Royal Society of Chemistry 2019-01-25 /pmc/articles/PMC9059925/ /pubmed/35518943 http://dx.doi.org/10.1039/c8ra09649j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wei, Yingying
Chen, Lin
Wang, Junli
Liu, Xuguang
Yang, Yongzhen
Yu, Shiping
Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title_full Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title_fullStr Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title_full_unstemmed Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title_short Investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
title_sort investigation on the chirality mechanism of chiral carbon quantum dots derived from tryptophan
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059925/
https://www.ncbi.nlm.nih.gov/pubmed/35518943
http://dx.doi.org/10.1039/c8ra09649j
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