Photochromic coordinative cages containing dynamic CN imine bonds are assembled from a dithienylethene-based aldehyde and tris-amine precursors via metallo-component self-assembly. The resulting metal-templated cages are then reduced and demetalated into pure covalent-organic cages (COCs), which are otherwise difficult to prepare via de novo organic synthesis. Both the obtained coordinative and covalent cages can be readily interconverted between the ring-open (o-isomer) and one-lateral ring-closed (c-isomer) forms by UV/vis light irradiation, demonstrating distinct absorption, luminescence and photoisomerization dynamics. Specifically, the ring-closed c-COCs show a blue-shifted absorption band compared with analogous metal-templated cages, which can be applied in photoluminescence (PL) color-tuning of upconversion materials in different ways, showing potential for constructing multi-readout logic gate systems. This journal is
CITATION STYLE
Zhang, J. H., Wang, H. P., Zhang, L. Y., Wei, S. C., Wei, Z. W., Pan, M., & Su, C. Y. (2020). Coordinative-to-covalent transformation, isomerization dynamics, and logic gate application of dithienylethene based photochromic cages. Chemical Science, 11(33), 8885–8894. https://doi.org/10.1039/d0sc03290e
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