3D‐Printable Shape‐Memory Polymers Based on Halogen Bond Interactions

GND
1214891268
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Meurer, Josefine;
GND
1298463238
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Kampes, Robin H.;
GND
1278269916
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Bätz, Thomas;
GND
1214890598
Zugehörigkeit
Institute of Physical Chemistry (IPC) Friedrich Schiller University Jena Helmholtzweg 4 07743 Jena Germany
Hniopek, Julian;
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Müschke, Oswald;
GND
1220243884
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Kimmig, Julian;
GND
1103575945
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Zechel, Stefan;
GND
120748193
Zugehörigkeit
Institute of Physical Chemistry (IPC) Friedrich Schiller University Jena Helmholtzweg 4 07743 Jena Germany
Schmitt, Michael;
GND
131701819
Zugehörigkeit
Jena Center for Soft Matter (JCSM) Friedrich Schiller University Jena Philosophenweg 7 07743 Jena Germany
Popp, Jürgen;
GND
134002695
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Hager, Martin D.;
GND
113792077
ORCID
0000-0003-4978-4670
Zugehörigkeit
Laboratory of Organic and Macromolecular Chemistry (IOMC) Friedrich Schiller University Jena Humboldstr 10 07743 Jena Germany
Schubert, Ulrich S.

The supramolecular halogen bonding (XB) is utilized for the first time for the preparation of shape‐memory polymers. For this purpose, an iodotriazole‐based bidentate XB donor featuring a methacrylamide is synthesized. Free radical polymerization of the XB donor monomer together with butyl methacrylate, triethylene glycole dimethacrylate, and methacrylic acid results in covalently cross‐linked polymer networks bearing both, halogen bond acceptors and donors, in their side chains. While the reversible halogen bond interactions can act as switching unit, the required stable phase of the shape‐memory polymers is formed by covalent cross‐links. The successful formation of the supramolecular cross‐links is proven via Fourier‐transform Raman spectroscopy. Furthermore, the thermal properties are investigated via differential scanning calorimetry and thermo gravimetric analysis. Thermo‐mechanical analysis reveals excellent shape‐memory abilities with fixity rates above 95% and recovery rates up to 99%. Moreover, it is possible to 3D‐print this kind of material exhibiting the ability to recover its shape within a few seconds at 130 °C.

Zitieren

Zitierform:
Zitierform konnte nicht geladen werden.

Rechte

Rechteinhaber: © 2022 Wiley‐VCH GmbH

Nutzung und Vervielfältigung: