Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/11000/31038

Influence of substituents of Perylenebisimides on the surface energy and wettability: A systematic structure–property relationship analysis


no-thumbnailVer/Abrir:

 Influence of substituents of Perylenebisimides on the surface energy and.pdf



2,54 MB
Adobe PDF
Compartir:

Este recurso está restringido

Título :
Influence of substituents of Perylenebisimides on the surface energy and wettability: A systematic structure–property relationship analysis
Autor :
Pérez-Ojeda, M.Eugenia
Zink Lorre, Nathalie
Pla, Sara
Sastre-Santos, Ángela
Fernández Lázaro, Fernando
Hirsch, Andreas  
Editor :
Elsevier
Departamento:
Departamentos de la UMH::Farmacología, Pediatría y Química Orgánica
Fecha de publicación:
2022
URI :
https://hdl.handle.net/11000/31038
Resumen :
This paper seeks to elucidate the influence on the surface wettability of a variety of substituents located in different positions of the perylene bisimide (PBI) core (ortho versus imide) with distinct electron-donor or -withdrawing character and diverse steric demand, using for this more than 20 planar PBIs. The correlation between the polarity of the individual functional group on the PBI and the surface wettability has been addressed by means of substituent descriptors in terms of Hansch-Fujita π parameter, Hammett σmeta and σpara constants, and steric parameters (Taft-Dubois Es’ and Charton υ). With these parameters, a quantitative structure–property relationship (QSPR) analysis has been performed using multivariable linear regression (MLR) fittings. The relationship of Surface Energy, determined by the static contact angle method with three different solvents, to structural properties of PBIs is described. As well, the polar and dispersive contributions have been determined. For planar PBIs, a predominant influence of the substituents in the imide position on the surface wettability has been found despite of the electronic nature and steric hindrance of the substituents simultaneously located in ortho positions. This effect is more pronounced with the longer alkyl substituents at the imide position. This study paves the way for a rational chromophore design considering the on surface behavior, which will ultimately condition the contact and thus their performance in optoelectronic devices.
Palabras clave/Materias:
Perylene bisimide
Contact angle
Wettability
Surface energy
Substituents descriptors
QSPR quantitative structure-property
relationship
Área de conocimiento :
CDU: Ciencias aplicadas: Medicina: Farmacología. Terapéutica. Toxicología. Radiología
Tipo documento :
application/pdf
Derechos de acceso:
info:eu-repo/semantics/closedAccess
DOI :
https://doi.org/10.1016/j.dyepig.2021.110044
Aparece en las colecciones:
Artículos Farmacología, Pediatría y Química Orgánica



Creative Commons La licencia se describe como: Atribución-NonComercial-NoDerivada 4.0 Internacional.