journal article·2022-04-13

Manipulation of Liquid Crystalline Properties by Dynamic Covalent Chemistry─En Route to Adaptive Materials

Meik Blanke, Leona Postulka, Isabelle Ciara, Francesco D’Acierno, Marcus Hildebrandt, Jochen S. Gutmann, Ronald Y. Dong, Carl A. Michal, Michael Giese

ACS Applied Materials & Interfaces· Volume 14· Issue 14
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Abstract

Dynamic covalent bonds bear great potential for the development of adaptive and self-healing materials. Herein, we introduce a versatile concept not only for the design of low-molecular-weight liquid crystals but also for their in situ postsynthetic modification by using the dynamic covalent nature of imine bonds. The methodology allows systematic investigations of structure–property relationships as well as the manipulation of the materials’ behavior (liquid crystallinity) and the introduction of additional properties (here, fluorescence) by a solvent-free method. For the first time, the transamination reaction is followed by variable-temperature 19F solid-state NMR in the mesophase, providing insights into the reaction dynamics in a liquid crystalline material. Finally, the application potential for the design of liquid crystalline materials with adaptive properties is demonstrated by a sequential combination of these reactions.
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Research context

OpenAlex topics: Supramolecular Chemistry and Complexes · Porphyrin and Phthalocyanine Chemistry · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Organic Chemistry, University of Duisburg-Essen, Universitätsstraße 7, 45117 Essen, Germany

Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver BC V6T 1Z1, Canada

Department of Physics and Astronomy, University of British Columbia, 6224 Agricultural Road, Vancouver BC V6T 1Z1, Canada

Physical Chemistry, University of Duisburg-Essen, Universitätsstraße 2, 45117 Essen, Germany

Funding

Natural Sciences and Engineering Research Council of Canada · Professor-Werdelmann Stiftung

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