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Plasticization of a Semicrystalline Metallosupramolecular Polymer Network
[Image: see text] The assembly of ligand-functionalized (macro)monomers with suitable metal ions affords metallosupramolecular polymers (MSPs). On account of the reversible and dynamic nature of the metal–ligand complexes, these materials can be temporarily (dis-)assembled upon exposure to a suitabl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912337/ https://www.ncbi.nlm.nih.gov/pubmed/36785838 http://dx.doi.org/10.1021/acspolymersau.2c00044 |
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author | Marx, Franziska Pal, Subhajit Sautaux, Julien Pallab, Nazim Stoclet, Grégory Weder, Christoph Schrettl, Stephen |
author_facet | Marx, Franziska Pal, Subhajit Sautaux, Julien Pallab, Nazim Stoclet, Grégory Weder, Christoph Schrettl, Stephen |
author_sort | Marx, Franziska |
collection | PubMed |
description | [Image: see text] The assembly of ligand-functionalized (macro)monomers with suitable metal ions affords metallosupramolecular polymers (MSPs). On account of the reversible and dynamic nature of the metal–ligand complexes, these materials can be temporarily (dis-)assembled upon exposure to a suitable stimulus, and this effect can be exploited to heal damaged samples, to facilitate processing and recycling, or to enable reversible adhesion. We here report on the plasticization of a semicrystalline, stimuli-responsive MSP network that was assembled by combining a low-molecular-weight building block carrying three 2,6-bis(1′-methylbenzimidazolyl) pyridine (Mebip) ligands and zinc bis(trifluoromethylsulfonyl)imide (Zn(NTf(2))(2)). The pristine material exhibits high melting (T(m) = 230 °C) and glass transition (T(g) ≈ 157 °C) temperatures and offers robust mechanical properties between these temperatures. We show that this regime can be substantially extended through plasticization. To achieve this, the MSP network was blended with diisodecyl phthalate. The weight fraction of this plasticizer was systematically varied, and the thermal and mechanical properties of the resulting materials were investigated. We show that the T(g) can be lowered by more than 60 °C and the toughness above the T(g) is considerably increased. |
format | Online Article Text |
id | pubmed-9912337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99123372023-02-11 Plasticization of a Semicrystalline Metallosupramolecular Polymer Network Marx, Franziska Pal, Subhajit Sautaux, Julien Pallab, Nazim Stoclet, Grégory Weder, Christoph Schrettl, Stephen ACS Polym Au [Image: see text] The assembly of ligand-functionalized (macro)monomers with suitable metal ions affords metallosupramolecular polymers (MSPs). On account of the reversible and dynamic nature of the metal–ligand complexes, these materials can be temporarily (dis-)assembled upon exposure to a suitable stimulus, and this effect can be exploited to heal damaged samples, to facilitate processing and recycling, or to enable reversible adhesion. We here report on the plasticization of a semicrystalline, stimuli-responsive MSP network that was assembled by combining a low-molecular-weight building block carrying three 2,6-bis(1′-methylbenzimidazolyl) pyridine (Mebip) ligands and zinc bis(trifluoromethylsulfonyl)imide (Zn(NTf(2))(2)). The pristine material exhibits high melting (T(m) = 230 °C) and glass transition (T(g) ≈ 157 °C) temperatures and offers robust mechanical properties between these temperatures. We show that this regime can be substantially extended through plasticization. To achieve this, the MSP network was blended with diisodecyl phthalate. The weight fraction of this plasticizer was systematically varied, and the thermal and mechanical properties of the resulting materials were investigated. We show that the T(g) can be lowered by more than 60 °C and the toughness above the T(g) is considerably increased. American Chemical Society 2022-11-10 /pmc/articles/PMC9912337/ /pubmed/36785838 http://dx.doi.org/10.1021/acspolymersau.2c00044 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Marx, Franziska Pal, Subhajit Sautaux, Julien Pallab, Nazim Stoclet, Grégory Weder, Christoph Schrettl, Stephen Plasticization of a Semicrystalline Metallosupramolecular Polymer Network |
title | Plasticization
of a Semicrystalline Metallosupramolecular
Polymer Network |
title_full | Plasticization
of a Semicrystalline Metallosupramolecular
Polymer Network |
title_fullStr | Plasticization
of a Semicrystalline Metallosupramolecular
Polymer Network |
title_full_unstemmed | Plasticization
of a Semicrystalline Metallosupramolecular
Polymer Network |
title_short | Plasticization
of a Semicrystalline Metallosupramolecular
Polymer Network |
title_sort | plasticization
of a semicrystalline metallosupramolecular
polymer network |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912337/ https://www.ncbi.nlm.nih.gov/pubmed/36785838 http://dx.doi.org/10.1021/acspolymersau.2c00044 |
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