Please use this identifier to cite or link to this item: https://repository.usc.edu.co/handle/20.500.12421/312
Title: Structural, spectroscopic, and theoretical analysis of a molecular system based on 2-((2-(4- chlorophenylhydrazone)methyl)quinolone
Other Titles: Análise estrutural, espectroscópico, e teórico de um sistema molecular com base na 2-((2-(4-Clorofenilhidrazona)metil)quinolina
Análisis estructural, espectroscópico y teórico de un sistema molecular basado en la 2-((2-(4-clorofenilhidrazono)metil)quinolina
Authors: Romero, Elkin L.
Soto-Monsalve, Mónica
Gutiérrez, Gustavo
Zuluaga, Fabio
D'Vries, Richard F.
Chaur, Manuel N.
Keywords: Configurational dynamic;DFT calculations;Electrochemistry;Hydrazone derivatives;Single XRD
Issue Date: 2-Dec-2018
Publisher: Universidad Nacional de Colombia
Abstract: A novel molecular system based on 2-((2-(4-chlorophenylhydrazone)methyl)quinoline (1-E) was synthesized. Interconversion of 1-E to its configurational isomer 1-Z was achieved using UV radiation (250 W Hg lamp). Such isomerization was monitored by1H-NMR. The results suggest that the hydrazone derivative can act as a chemical brake in solution. This molecular system was structurally (Single Crystal X-Ray diffraction and DFT calculations) and spectroscopically (NMR, UV, and IR) characterized. Electrochemical measurements showed that configurational changes induce differential redox behavior. In this regard, the reported quinoline system exhibits different dynamic absorption and electrochemical properties that are modulated by UV-light. Therefore, 1-E can be regarded as a potential photo-electrochemical switch. © 2018, Universidad Nacional de Colombia. All rights reserved.
URI: https://repository.usc.edu.co/handle/20.500.12421/312
ISSN: 01202804
Appears in Collections:Artículos Científicos



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