Issue 34, 2021

Cochineal quinone carbon dot synthesis via a keto–enol tautomerism strategy and their intermolecular photo-induced cross-redox interactions with tetracycline

Abstract

Natural product-originated carbon dots represent a charming and valuable platform for bio-fluorescence probes; however, the application scope of these probes is seriously restricted, due to the indistinct molecular structures of these bio-probes and the inaccurate interactions between the probe and detected guest molecule. Herein, a novel strategy of keto–enol tautomerism-mediated quinone aromatization has been achieved for Cochineal bio-based quinone carbon dot synthesis. Then, a photo-induced intermolecular cross-redox reaction was accomplished with tetracycline for quinone carbon dot molecule transformation and fluorescence change. This work represents a pioneer for intermolecular interaction simulation and bonding energy evaluation of carbon dots for trace organics detection.

Graphical abstract: Cochineal quinone carbon dot synthesis via a keto–enol tautomerism strategy and their intermolecular photo-induced cross-redox interactions with tetracycline

Supplementary files

Article information

Article type
Paper
Submitted
02 Jun 2021
Accepted
23 Jul 2021
First published
24 Jul 2021

New J. Chem., 2021,45, 15336-15343

Cochineal quinone carbon dot synthesis via a keto–enol tautomerism strategy and their intermolecular photo-induced cross-redox interactions with tetracycline

Y. Tao, Y. He, J. Ye, X. Yang, Y. Yang, G. Xie, L. Liu, G. Du, H. Zhang and B. Zhou, New J. Chem., 2021, 45, 15336 DOI: 10.1039/D1NJ02701H

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