Donor–Acceptor Stenhouse Adduct‐Polydimethylsiloxane‐Conjugates for Enhanced Photoswitching in Bulk Polymers

Abstract: Donor–acceptor Stenhouse adducts (DASAs) are a rapidly emerging class of visible light‐activated photochromes and DASA‐functionalized polymers hold great promise as biocompatible photoresponsive materials. However, the photoswitching performance of DASAs in solid polymer matrices is often low, particularly in materials below their glass transition temperature. To overcome this limitation, DASAs are conjugated to polydimethylsiloxanes which have a glass transition temperature far below room temperature and which can create a mobile molecular environment around the DASAs for achieving more solution‐like photoswitching kinetics in bulk polymers. The dispersion of DASAs conjugated to such flexible oligomers into solid polymer matrices allows for more effective and tunable DASA photoswitching in stiff polymers, such as poly (methyl methacrylate), without requiring modifications of the matrix. The photoswitching of conjugates with varying polymer molecular weight, linker type, and architecture is characterized via time‐dependent UV–vis spectroscopy in organic solvents and blended into polymethacrylate films. In addition, DASA‐functionalized polydimethylsiloxane networks, accessible via the same synthetic route, provide an alternative solution for achieving fast and efficient DASA photoswitching in the bulk owing to their intrinsic softness and flexibility. These findings may contribute to the development of DASA‐functionalized materials with better tunable, more effective, and more reversible modulation of their optical properties.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Donor–Acceptor Stenhouse Adduct‐Polydimethylsiloxane‐Conjugates for Enhanced Photoswitching in Bulk Polymers ; day:01 ; month:05 ; year:2022 ; extent:13
Macromolecular rapid communications ; (01.05.2022) (gesamt 13)

Urheber
Clerc, Michèle
Tekin, Cem
Ulrich, Sebastian
Freire, Rafael V. M.
Salentinig, Stefan
Bruns, Nico
Boesel, Luciano F.

DOI
10.1002/marc.202200120
URN
urn:nbn:de:101:1-2022050215054568271809
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:35 MESZ

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