Construction of Multi‐Stimuli Responsive Highly Porous Switchable Frameworks by In Situ Solid‐State Generation of Spiropyran Switches

Author:

Sheng Jinyu1ORCID,Perego Jacopo2ORCID,Bracco Silvia2ORCID,Czepa Włodzimierz34,Danowski Wojciech15ORCID,Krause Simon16ORCID,Sozzani Piero2ORCID,Ciesielski Artur45ORCID,Comotti Angiolina2ORCID,Feringa Ben L.1ORCID

Affiliation:

1. Stratingh Institute for Chemistry University of Groningen Groningen, the Netherlands. Nijenborgh 4 Groningen AG 9747 The Netherlands

2. Department of Materials Science University of Milano Bicocca Milan, Italy. Via R. Cozzi 55 Milan 20125 Italy

3. Faculty of Chemistry Adam Mickiewicz University Uniwersytetu Poznańskiego 8 Poznań 61614 Poland

4. Center for Advanced Technologies Adam Mickiewicz University Uniwersytetu Poznańskiego 10 Poznań 61614 Poland

5. Université de Strasbourg CNRS ISIS 8 allée Gaspard Monge Strasbourg 67000 France

6. Nanochemistry Department Max Planck Institute for Solid State Research Heisenbergstr. 1 70569 Stuttgart Germany

Abstract

AbstractStimuli‐responsive molecular systems support within permanently porous materials offer the opportunity to host dynamic functions in multifunctional smart materials. However, the construction of highly porous frameworks featuring external‐stimuli responsiveness, for example by light excitation, is still in its infancy. Here a general strategy is presented to construct spiropyran‐functionalized highly porous switchable aromatic frameworks by modular and high‐precision anchoring of molecular hooks and an innovative in situ solid‐state grafting approach. Three spiropyran‐grafted frameworks bearing distinct functional groups exhibiting various stimuli‐responsiveness are generated by two‐step post‐solid‐state synthesis of a parent indole‐based material. The quantitative transformation and preservation of high porosity are demonstrated by spectroscopic and gas adsorption techniques. For the first time, a highly efficient strategy is provided to construct multi‐stimuli‐responsive, yet structurally robust, spiropyran materials with high pore capacity which is proved essential for the reversible and quantitative isomerization in the bulk as demonstrated by solid‐state NMR spectroscopy. The overall strategy allows to construct dynamic materials that undergoes reversible transformation of spiropyran to zwitterionic merocyanine, by chemical and physical stimulation, showing potential for pH active control, responsive gas uptake and release, contaminant removal, and water harvesting.

Funder

China Scholarship Council

European Research Council

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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