Cargando…

Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly

This joint experimental-theoretical work focuses on molecular and photophysical properties of the spiropyran-containing amphiphilic molecule in organic and aqueous solutions. Being dissolved in tested organic solvents, the system demonstrates positive photochromism, i.e., upon UV stimulus the colorl...

Descripción completa

Detalles Bibliográficos
Autores principales: Savchenko, Vladyslav, Lomadze, Nino, Santer, Svetlana, Guskova, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569490/
https://www.ncbi.nlm.nih.gov/pubmed/36232836
http://dx.doi.org/10.3390/ijms231911535
_version_ 1784809866669326336
author Savchenko, Vladyslav
Lomadze, Nino
Santer, Svetlana
Guskova, Olga
author_facet Savchenko, Vladyslav
Lomadze, Nino
Santer, Svetlana
Guskova, Olga
author_sort Savchenko, Vladyslav
collection PubMed
description This joint experimental-theoretical work focuses on molecular and photophysical properties of the spiropyran-containing amphiphilic molecule in organic and aqueous solutions. Being dissolved in tested organic solvents, the system demonstrates positive photochromism, i.e., upon UV stimulus the colorless spiropyran form is transformed into colorful merocyanine isomer. However, the aqueous solution of the amphiphile possesses a negative photochromism: the orange-red merocyanine form becomes thermodynamically more stable in water, and both UV and vis stimuli lead to the partial or complete photobleaching of the solution. The explanation of this phenomenon is given on the basis of density functional theory calculations and classical modeling including thermodynamic integration. The simulations reveal that stabilization of merocyanine in water proceeds with the energy of ca. 70 kJ mol [Formula: see text] , and that the Helmholtz free energy of hydration of merocyanine form is 100 kJ mol [Formula: see text] lower as compared to the behavior of SP isomer in water. The explanation of such a difference lies in the molecular properties of the merocyanine: after ring-opening reaction this molecule transforms into a zwitterionic form, as evidenced by the electrostatic potential plotted around the opened form. The presence of three charged groups on the periphery of a flat conjugated backbone stimulates the self-assembly of merocyanine molecules in water, ending up with the formation of elongated associates with stack-like building blocks, as shown in molecular dynamics simulations of the aqueous solution with the concentration above critical micelle concentration. Our quantitative evaluation of the hydrophilicity switching in spiropyran/merocyanine containing surfactants may prompt the search for new systems, including colloidal and polymeric ones, aiming at remote tuning of their morphology, which could give new promising shapes and patterns for the needs of modern nanotechnology.
format Online
Article
Text
id pubmed-9569490
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95694902022-10-17 Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly Savchenko, Vladyslav Lomadze, Nino Santer, Svetlana Guskova, Olga Int J Mol Sci Article This joint experimental-theoretical work focuses on molecular and photophysical properties of the spiropyran-containing amphiphilic molecule in organic and aqueous solutions. Being dissolved in tested organic solvents, the system demonstrates positive photochromism, i.e., upon UV stimulus the colorless spiropyran form is transformed into colorful merocyanine isomer. However, the aqueous solution of the amphiphile possesses a negative photochromism: the orange-red merocyanine form becomes thermodynamically more stable in water, and both UV and vis stimuli lead to the partial or complete photobleaching of the solution. The explanation of this phenomenon is given on the basis of density functional theory calculations and classical modeling including thermodynamic integration. The simulations reveal that stabilization of merocyanine in water proceeds with the energy of ca. 70 kJ mol [Formula: see text] , and that the Helmholtz free energy of hydration of merocyanine form is 100 kJ mol [Formula: see text] lower as compared to the behavior of SP isomer in water. The explanation of such a difference lies in the molecular properties of the merocyanine: after ring-opening reaction this molecule transforms into a zwitterionic form, as evidenced by the electrostatic potential plotted around the opened form. The presence of three charged groups on the periphery of a flat conjugated backbone stimulates the self-assembly of merocyanine molecules in water, ending up with the formation of elongated associates with stack-like building blocks, as shown in molecular dynamics simulations of the aqueous solution with the concentration above critical micelle concentration. Our quantitative evaluation of the hydrophilicity switching in spiropyran/merocyanine containing surfactants may prompt the search for new systems, including colloidal and polymeric ones, aiming at remote tuning of their morphology, which could give new promising shapes and patterns for the needs of modern nanotechnology. MDPI 2022-09-29 /pmc/articles/PMC9569490/ /pubmed/36232836 http://dx.doi.org/10.3390/ijms231911535 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Savchenko, Vladyslav
Lomadze, Nino
Santer, Svetlana
Guskova, Olga
Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title_full Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title_fullStr Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title_full_unstemmed Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title_short Spiropyran/Merocyanine Amphiphile in Various Solvents: A Joint Experimental–Theoretical Approach to Photophysical Properties and Self-Assembly
title_sort spiropyran/merocyanine amphiphile in various solvents: a joint experimental–theoretical approach to photophysical properties and self-assembly
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569490/
https://www.ncbi.nlm.nih.gov/pubmed/36232836
http://dx.doi.org/10.3390/ijms231911535
work_keys_str_mv AT savchenkovladyslav spiropyranmerocyanineamphiphileinvarioussolventsajointexperimentaltheoreticalapproachtophotophysicalpropertiesandselfassembly
AT lomadzenino spiropyranmerocyanineamphiphileinvarioussolventsajointexperimentaltheoreticalapproachtophotophysicalpropertiesandselfassembly
AT santersvetlana spiropyranmerocyanineamphiphileinvarioussolventsajointexperimentaltheoreticalapproachtophotophysicalpropertiesandselfassembly
AT guskovaolga spiropyranmerocyanineamphiphileinvarioussolventsajointexperimentaltheoreticalapproachtophotophysicalpropertiesandselfassembly