Preparation of water-insoluble inorganic-organic photochromic hybrid compound [Ni(1,10-phen)3]3(PMo12O40)2 by simple chemical co-precipitation method
Xu, Hang; Chi, Xi; Li, Feng; Li, Taohai (2025-08-26)
Xu, Hang
Chi, Xi
Li, Feng
Li, Taohai
Elsevier
26.08.2025
Xu, H., Chi, X., Li, F., & Li, T. (2025). Preparation of water-insoluble inorganic-organic photochromic hybrid compound [Ni(1,10-phen)3]3(Pmo12o40)2 by simple chemical co-precipitation method. Results in Chemistry, 17, 102637. https://doi.org/10.1016/j.rechem.2025.102637
https://creativecommons.org/licenses/by/4.0/
© 2025 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
© 2025 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202509035723
https://urn.fi/URN:NBN:fi:oulu-202509035723
Tiivistelmä
Abstract
The conventional polyoxometalate utilized in inorganic photochromic materials are noted for their exceptional stability; however, they exhibit certain deficiencies, such as difficulties during processing and elevated solubility, which hinder their application in practical scenarios. In contrast, the distinctive structural features of polypyridine ligands, coupled with their remarkable photosensitivity, serve to effectively mitigate the shortcomings encountered with polymetallic oxides. In this study, we successfully synthesized inorganic-organic photochromic hybrid compounds, specifically [Ni(1,10-phen)3]3(PMo12O40)2, utilizing a straightforward chemical co-precipitation methodology. The resultant samples were characterized in three distinct physical forms: powder, film, and solution. Notably, upon exposure to UV light, these compounds exhibited a rapid chromatic transition from bright yellow to deep green within a mere ten minutes. The swift colorimetric response properties of these hybrids indicate their substantial potential for diverse industrial applications, particularly in dynamic optical devices and smart materials.
The conventional polyoxometalate utilized in inorganic photochromic materials are noted for their exceptional stability; however, they exhibit certain deficiencies, such as difficulties during processing and elevated solubility, which hinder their application in practical scenarios. In contrast, the distinctive structural features of polypyridine ligands, coupled with their remarkable photosensitivity, serve to effectively mitigate the shortcomings encountered with polymetallic oxides. In this study, we successfully synthesized inorganic-organic photochromic hybrid compounds, specifically [Ni(1,10-phen)3]3(PMo12O40)2, utilizing a straightforward chemical co-precipitation methodology. The resultant samples were characterized in three distinct physical forms: powder, film, and solution. Notably, upon exposure to UV light, these compounds exhibited a rapid chromatic transition from bright yellow to deep green within a mere ten minutes. The swift colorimetric response properties of these hybrids indicate their substantial potential for diverse industrial applications, particularly in dynamic optical devices and smart materials.
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