Spontaneous Long‐Range Order and Alignment in Phase‐Separated Dynamic Covalent Networks Using Discrete Siloxanes

S Stefan J. D. Maessen (Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands) T Tymen M. L. van der Leede (Department of Chemical Engineering & Chemistry and Institute for Complex Molecular Systems Eindhoven University of Technology Eindhoven the Netherlands) A Anne B. Spoelstra (Department of Chemical Engineering & Chemistry and Center for Multiscale Electron Microscopy Eindhoven University of Technology Eindhoven the Netherlands) B Bart W. L. van den Bersselaar (Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands) B Bas F. M. de Waal (Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands) J Johan P. A. Heuts A Anja R. A. Palmans (Department of Chemistry, Johannes Gutenberg University Mainz)

Abstract

ABSTRACT For the first time, dynamic covalent networks are prepared that show spontaneous alignment and long‐range hexagonal columnar ordering. This is a consequence of the phase‐separation between the siloxane linkers and dynamic covalent acylsemicarbazide bonds that induce hydrogen bonding. The use of discrete siloxane linkers is crucial, as networks based on disperse siloxanes do not give ordered or aligned network structures. Optimization of the siloxane length is key in achieving the most pronounced effect. Interestingly, the optimized ordered networks are obtained through simple solvent evaporation, allowing to introduce near‐perfect homeotropic alignment as imaged with transmission electron microscopy and corroborated with grazing incidence small angle x‐ray scattering. The ordered network has improved (thermo)mechanical properties compared to the disordered networks. Additionally, order in the system slows down the network dynamics and improves creep resistance. We prepare actuators in a straightforward fashion by combining ordered and disordered networks, removing the need for any alignment step and simplifying the overall process significantly.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 31, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

S

Stefan J. D. Maessen

Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands

T

Tymen M. L. van der Leede

Department of Chemical Engineering & Chemistry and Institute for Complex Molecular Systems Eindhoven University of Technology Eindhoven the Netherlands

A

Anne B. Spoelstra

Department of Chemical Engineering & Chemistry and Center for Multiscale Electron Microscopy Eindhoven University of Technology Eindhoven the Netherlands

B

Bart W. L. van den Bersselaar

Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands

B

Bas F. M. de Waal

Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600MB Eindhoven, The Netherlands

J

Johan P. A. Heuts

A

Anja R. A. Palmans

Department of Chemistry, Johannes Gutenberg University Mainz