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New Insights into Acylhydrazones E/Z Isomerization: An Experimental and Theoretical Approach †

A family of acylhydrazones have been prepared and characterized with the aim of investigating their potential as information storage systems. Their well-established synthetic methodologies allowed for the preparation of seven chemically stable acylhydrazones in excellent yields that have been photop...

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Detalles Bibliográficos
Autores principales: Fernández-Palacios, Sara, Matamoros, Esther, Morato Rojas, Isabel, López Navarrete, Juan T., Ruiz Delgado, M. Carmen, Vida, Yolanda, Perez-Inestrosa, Ezequiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648745/
https://www.ncbi.nlm.nih.gov/pubmed/37834186
http://dx.doi.org/10.3390/ijms241914739
Descripción
Sumario:A family of acylhydrazones have been prepared and characterized with the aim of investigating their potential as information storage systems. Their well-established synthetic methodologies allowed for the preparation of seven chemically stable acylhydrazones in excellent yields that have been photophysically and photochemically characterized. In addition, DFT and TD-DFT calculations have been performed to gain more insights into the structural, energetic and photophysical properties of the E/Z isomers. Our results reveal that E/Z configurational isomerization upon irradiation is highly dependent on the stabilization of the E or Z isomers due to the formation of intramolecular H bonds and the electronic/steric effects intrinsically related to their structures. In addition, Raman spectroscopy is also used to confirm the molecular structural changes after the formation of hydrogen bonds in the isomers.