Tunable UCST behaviour of a hydrophobic ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Tunable UCST behaviour of a hydrophobic dialkoxynaphthalene-functionalized homopolymer based on reversible supramolecular recognition
Auteur(s) :
Guan, Xinran [Auteur]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Vebr, Aurelien [Auteur]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Hoogenboom, Richard [Auteur]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Vebr, Aurelien [Auteur]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Hoogenboom, Richard [Auteur]
Universiteit Gent = Ghent University = Université de Gand [UGENT]
Titre de la revue :
European Polymer Journal
Nom court de la revue :
European Polymer Journal
Pagination :
112549
Éditeur :
Elsevier BV
Date de publication :
2023-12-11
ISSN :
0014-3057
Discipline(s) HAL :
Chimie/Matériaux
Chimie/Polymères
Chimie/Polymères
Résumé en anglais : [en]
Thermoresponsive polymers with reversible phase transition are appealing to various applications. Herein, we designed and synthesized a thermosensitive homopolymer bearing hydrophobic dialkoxynaphthalene moieties as polymer ...
Lire la suite >Thermoresponsive polymers with reversible phase transition are appealing to various applications. Herein, we designed and synthesized a thermosensitive homopolymer bearing hydrophobic dialkoxynaphthalene moieties as polymer side chains that revealed UCST behaviour in pure ethanol and ethanol/water mixtures. It is reported that the complexation with the tetracationic macrocycle cyclobis(paraquat-p-phenylene) (CBPQT4+) host is strongly dependent on the degree of complexation due to steric hindrance and charge repulsion. Moreover, it was found that the cloud-point temperatures (TCP) of the homopolymer could be modulated by host–guest complexation with CBPQT4+ in alcohol-water solvent mixtures up to 6 equivalents of the host. When heated above the clearance-point temperatures, the homopolymer dissolves, but the host–guest interactions become unstable and are disrupted due to the effect of the solvent and the higher temperature. Subsequent cooling led to the collapse of the homopolymer, together with the reformation of the host–guest complexes resulting in a purple opaque solution. The tunable UCST approach may enable practical applications in the biomedical field or interactive smart materials.Lire moins >
Lire la suite >Thermoresponsive polymers with reversible phase transition are appealing to various applications. Herein, we designed and synthesized a thermosensitive homopolymer bearing hydrophobic dialkoxynaphthalene moieties as polymer side chains that revealed UCST behaviour in pure ethanol and ethanol/water mixtures. It is reported that the complexation with the tetracationic macrocycle cyclobis(paraquat-p-phenylene) (CBPQT4+) host is strongly dependent on the degree of complexation due to steric hindrance and charge repulsion. Moreover, it was found that the cloud-point temperatures (TCP) of the homopolymer could be modulated by host–guest complexation with CBPQT4+ in alcohol-water solvent mixtures up to 6 equivalents of the host. When heated above the clearance-point temperatures, the homopolymer dissolves, but the host–guest interactions become unstable and are disrupted due to the effect of the solvent and the higher temperature. Subsequent cooling led to the collapse of the homopolymer, together with the reformation of the host–guest complexes resulting in a purple opaque solution. The tunable UCST approach may enable practical applications in the biomedical field or interactive smart materials.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
INRAE
ENSCL
CNRS
INRAE
ENSCL
Collections :
Équipe(s) de recherche :
Ingénierie des Systèmes Polymères
Date de dépôt :
2023-12-19T06:39:24Z
2023-12-20T13:31:09Z
2023-12-20T13:32:19Z
2023-12-20T13:31:09Z
2023-12-20T13:32:19Z