Your browser doesn't support javascript.
loading
Near Infrared Light-Driven Photothermal Effect on Homochiral Au/TiO2 Nanotube Arrays for Enantioselective Desorption.
Qu, Kuanzhi; Xu, Jing; Xue, Yuanfei; Guo, Junli; Gao, Zhida; Song, Yan-Yan; Mei, Ye.
Afiliação
  • Qu K; College of Sciences, Northeastern University, Shenyang 110819, China.
  • Xu J; College of Sciences, Northeastern University, Shenyang 110819, China.
  • Xue Y; State Key Laboratory of Precision Spectroscopy, School of Physics and Electronic Science, East China Normal University, Shanghai 200062, China.
  • Guo J; NYU-ECNU Center for Computational Chemistry at NYU Shanghai, Shanghai 200062, China.
  • Gao Z; Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan, Shanxi 030006, China.
  • Song YY; College of Sciences, Northeastern University, Shenyang 110819, China.
  • Mei Y; College of Sciences, Northeastern University, Shenyang 110819, China.
Anal Chem ; 94(2): 588-592, 2022 01 18.
Article em En | MEDLINE | ID: mdl-34931801
ABSTRACT
Chiral enantiomers have different effects on biological processes. Enantiomer separation is significant and necessary. Herein, a photothermal (PT) effect-derived enantioselective desorption strategy based on homochiral Au/TiO2 nanotubes (NTs) is developed. Using 3,4-dihydroxyphenylalanine (DOPA) as the model enantiomer, an obvious selective desorption of L/D-DOPA can be achieved by the NIR light-triggered local temperature enhancement. Molecular docking simulation further verifies that the distinct affinity precipitated by the different hydrogen bonds between homochiral sorbent and target enantiomers is the origin of enantioselective desorption. This desorption strategy provides a green and alternative approach for the selective separation of chiral molecules.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanotubos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanotubos Idioma: En Ano de publicação: 2022 Tipo de documento: Article