Thermoresponsive polymers and host-guest ...
Document type :
Autre communication scientifique (congrès sans actes - poster - séminaire...): Communication dans un congrès sans actes
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Title :
Thermoresponsive polymers and host-guest chemistry: a win-win combination
Author(s) :
Ribeiro, Cedric [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
guo, hui [Auteur]
Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris [ESPCI Paris]
De Smet, Lieselot [Auteur]
Universiteit Gent = Ghent University [UGENT]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Belal, Khaled [Auteur]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Ingénierie des Systèmes Polymères
Vebr, Aurelien [Auteur]
1002334|||Unité Matériaux et Transformations - UMR 8207 [UMET]
Universiteit Gent = Ghent University [UGENT]
Malfait, aurélie [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Le Fer, Gaëlle [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Lyskawa, Joel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Potier, Jonathan [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Hourdet, Dominique [Auteur]
Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris [ESPCI Paris]
Stoffelbach, François [Auteur]
1140|||Chimie des polymères [LCP]
Marcellan, Alba [Auteur]
Chimie des polymères [LCP]
Hoogenboom, Richard [Auteur]
Universiteit Gent = Ghent University [UGENT]
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Ingénierie des Systèmes Polymères
Unité Matériaux et Transformations (UMET) - UMR 8207
guo, hui [Auteur]
Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris [ESPCI Paris]
De Smet, Lieselot [Auteur]
Universiteit Gent = Ghent University [UGENT]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Belal, Khaled [Auteur]
Unité Matériaux et Transformations - UMR 8207 [UMET]
Ingénierie des Systèmes Polymères
Vebr, Aurelien [Auteur]
1002334|||Unité Matériaux et Transformations - UMR 8207 [UMET]
Universiteit Gent = Ghent University [UGENT]
Malfait, aurélie [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Le Fer, Gaëlle [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Lyskawa, Joel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Potier, Jonathan [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Hourdet, Dominique [Auteur]
Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris [ESPCI Paris]
Stoffelbach, François [Auteur]
1140|||Chimie des polymères [LCP]
Marcellan, Alba [Auteur]
Chimie des polymères [LCP]
Hoogenboom, Richard [Auteur]
Universiteit Gent = Ghent University [UGENT]
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Ingénierie des Systèmes Polymères
Conference title :
51ème Edition du Colloque National du Groupe Français des Polymères (GFP)
City :
Bordeaux - Talence
Country :
France
Start date of the conference :
2023-11-20
English keyword(s) :
Thermoresponsive polymers
Host-guest complexation
memory function
synergistic control of the host reactivity
Host-guest complexation
memory function
synergistic control of the host reactivity
HAL domain(s) :
Chimie/Matériaux
Chimie/Polymères
Chimie/Polymères
English abstract : [en]
The combination of heat-sensitivepolymers and supramolecular chemistry has recently led to the development of fascinating adaptive materials. In this context, most studies have focused on exploiting host-guest interactions ...
Show more >The combination of heat-sensitivepolymers and supramolecular chemistry has recently led to the development of fascinating adaptive materials. In this context, most studies have focused on exploiting host-guest interactions to control the physicochemical properties of polymeric materials.1 This approach has notably enabled the creation of materials with programmable thermosensitivity and sensor properties.2 In contrast, the exploitation of polymer thermoresponsiveness to control the recognition properties of host-guest systems at the molecular level is much less developed, and a perfect understanding of the mechanisms triggering thermo-induced decomplexation or complexation is still elusive. In this communication, we will illustrate through three studies how the host-guest chemistry and the thermo-induced phase separation mechanisms can “talk together” to synergistically tune the coil↔globule transition and the complexation state of polymeric systems. The first example3 concerns a comparative analysis of the behaviour of complexes formed from different naphthalene end-functionalized LCST or UCST polymers and the electron-deficient cyclobis(paraquat-p-phenylene) tetrachloride (CBPQT4+, 4Cl-)3 host when subjected to heat treatment. This study provided an understanding of the mechanisms triggering the thermo-induced (de)complexation of such complexes. The second study reports a supramolecular approach for developing an intelligent thermoresponsive polymeric hydrogel featuring a dual temperature and time memory function based on a kinetic control of the material's (de)complexation and (re) swelling behaviours. The last study illustrates how a thermo-induced phase separation mechanism can regulate on demand the Diels-alder reactivity of a synthetic self-complexing host-guest molecular switch CBPQT4+-Fu, consisting of an electron-rich furan unit covalently attached to the electron-deficient CBPQT4+host, with maleimide in water. Thanks to a supramolecular control over the topology of CBPQT4+-Fu combined with a thermoresponsive supramolecular regulator, we reported a rare example of decreased reactivity upon increasing temperature.Show less >
Show more >The combination of heat-sensitivepolymers and supramolecular chemistry has recently led to the development of fascinating adaptive materials. In this context, most studies have focused on exploiting host-guest interactions to control the physicochemical properties of polymeric materials.1 This approach has notably enabled the creation of materials with programmable thermosensitivity and sensor properties.2 In contrast, the exploitation of polymer thermoresponsiveness to control the recognition properties of host-guest systems at the molecular level is much less developed, and a perfect understanding of the mechanisms triggering thermo-induced decomplexation or complexation is still elusive. In this communication, we will illustrate through three studies how the host-guest chemistry and the thermo-induced phase separation mechanisms can “talk together” to synergistically tune the coil↔globule transition and the complexation state of polymeric systems. The first example3 concerns a comparative analysis of the behaviour of complexes formed from different naphthalene end-functionalized LCST or UCST polymers and the electron-deficient cyclobis(paraquat-p-phenylene) tetrachloride (CBPQT4+, 4Cl-)3 host when subjected to heat treatment. This study provided an understanding of the mechanisms triggering the thermo-induced (de)complexation of such complexes. The second study reports a supramolecular approach for developing an intelligent thermoresponsive polymeric hydrogel featuring a dual temperature and time memory function based on a kinetic control of the material's (de)complexation and (re) swelling behaviours. The last study illustrates how a thermo-induced phase separation mechanism can regulate on demand the Diels-alder reactivity of a synthetic self-complexing host-guest molecular switch CBPQT4+-Fu, consisting of an electron-rich furan unit covalently attached to the electron-deficient CBPQT4+host, with maleimide in water. Thanks to a supramolecular control over the topology of CBPQT4+-Fu combined with a thermoresponsive supramolecular regulator, we reported a rare example of decreased reactivity upon increasing temperature.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Related reference(s) :
Administrative institution(s) :
Université de Lille
CNRS
INRAE
ENSCL
CNRS
INRAE
ENSCL
Collections :
Research team(s) :
Ingénierie des Systèmes Polymères
Submission date :
2023-12-19T08:10:28Z
2023-12-20T13:52:33Z
2023-12-20T13:52:33Z
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