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Stetsiuk, O., Bolle, P., Cordier, M., Boixel, J. & Dessapt, R. (2022) Structure-property relationships in normal and mixed dithienylethenes - polyoxometalates supramolecular assemblies with fast solid-state photochromic properties. J. Mater. Chem. C, 10 899–907. 
Added by: Richard Baschera (2021-12-16 10:28:52)   Last edited by: Richard Baschera (2022-07-22 08:18:56)
Type de référence: Article
DOI: 10.1039/D1TC04561J
Numéro d'identification (ISBN etc.): 2050-7534
Clé BibTeX: Stetsiuk2022
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Catégories: MIOPS
Créateurs: Boixel, Bolle, Cordier, Dessapt, Stetsiuk
Collection: J. Mater. Chem. C
Consultations : 17/350
Indice de consultation : 8%
Indice de popularité : 2%
Liens URLs     https://pubs.rsc.o ... 2022/tc/d1tc04561j
Résumé     
Five new highly photochromic hybrid organic–inorganic materials were successfully prepared by supramolecular assembly of normal (1+) and mixed (2+) cationic dithienylethenes (DTEs) and polyoxometalates (POMs) units. Single-crystal X-ray diffraction studies reveal that (1)3[PM12O40]·5ACN (M = W, Mo) (1-PW12 and 1-PMo12) and (2)3[PM12O40]·5ACN (M = W, Mo) (2-PW12 and 2-PMo12) are isostructural, while (2)4[Mo8O26]·4DMF (2-Mo8) is an isotype of (1)4[Mo8O26]·4DMF (1-Mo8) i.e., the first POM–DTE ionic assembly, recently reported. The solid-state photochromic properties of these materials at room temperature are highly tunable with the nature of the DTEs and POMs used, which has been interpreted taking into account steric and electronic factors. Especially, while 1-PMo12 and 2-PMo12 exhibit negligible photoresponses which have not been considered herein, thorough investigations of the photocoloration and fading kinetics in ambient conditions have highlighted the precise impact of both organic and inorganic components on the photoswitching abilities of 1-Mo8, 2-Mo8, 1-PW12 and 2-PW12. Upon UV-light irradiation, the absorption of the normal and mixed DTEs in their closed-ring form exhibits a hypsochromic shift which is more pronounced in hybrid systems integrating β-[Mo8O26]4− rather than α-[PW12O40]3−, due to the higher negative charge density of the octamolybdate unit. The photocyclization rates of DTEs are also systematically increased when combined with the β-[Mo8O26]4− unit, while in contrast, their back cycloreversion rates are not affected whatever the nature of the POMs used. In addition, within isostructural series, hybrids integrating mixed DTEs exhibit faster fading processes than their normal DTE counterparts when exposed to visible light. Finally, among this new series, 2-Mo8 shows the best photochromic performances with a fast photocoloration rate associated with a high coloration contrast, a fast and complete fading process and a high cyclability.
  
Notes     
Publisher: The Royal Society of Chemistry
  
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