Hybrid nanostructures with switchable and reversible “blue-red-green” emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions. The complexes were characterized by UV-Vis and fluorescence spectroscopy and their stoichiometry was also confirmed by 1H NMR spectroscopy. In the presence of the Eu(III) ions, the octafunctionalized nanocages self-assemble to form 3D architectures that display an intense red-emission, especially in the solid state. The presence of an alkenyl group bridging the inorganic core to the organic moiety was employed to tune the emission properties by trans-cis isomerization of the double bond. In the case of the octafunctionalized nanocages (O-POSS), this isomerization was monitored in the presence of Eu(III) cations and was accompanied by an evident colour change from blue (trans-O-POSS) to red (Eu@trans-O-POSS) and finally to green (cis-O-POSS) as consequence of the release of the metal cations. This behaviour, together with the easy dispersion of the dry powder and the possibility of coating as a film in presence of small amounts of solvent, makes the emissive solid promising for applications in materials science.

Cina V., Carbonell E., Fusaro L., Garcia H., Gruttadauria M., Giacalone F., et al. (2020). Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible trans-to-cis Isomerization. CHEMPLUSCHEM, 85(3), 391-398 [10.1002/cplu.201900575].

Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible trans-to-cis Isomerization

Cina V.
Investigation
;
Gruttadauria M.
Conceptualization
;
Giacalone F.
Conceptualization
;
2020-01-01

Abstract

Hybrid nanostructures with switchable and reversible “blue-red-green” emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions. The complexes were characterized by UV-Vis and fluorescence spectroscopy and their stoichiometry was also confirmed by 1H NMR spectroscopy. In the presence of the Eu(III) ions, the octafunctionalized nanocages self-assemble to form 3D architectures that display an intense red-emission, especially in the solid state. The presence of an alkenyl group bridging the inorganic core to the organic moiety was employed to tune the emission properties by trans-cis isomerization of the double bond. In the case of the octafunctionalized nanocages (O-POSS), this isomerization was monitored in the presence of Eu(III) cations and was accompanied by an evident colour change from blue (trans-O-POSS) to red (Eu@trans-O-POSS) and finally to green (cis-O-POSS) as consequence of the release of the metal cations. This behaviour, together with the easy dispersion of the dry powder and the possibility of coating as a film in presence of small amounts of solvent, makes the emissive solid promising for applications in materials science.
2020
Cina V., Carbonell E., Fusaro L., Garcia H., Gruttadauria M., Giacalone F., et al. (2020). Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible trans-to-cis Isomerization. CHEMPLUSCHEM, 85(3), 391-398 [10.1002/cplu.201900575].
File in questo prodotto:
File Dimensione Formato  
79. ChemPlusChem2020,85, 391–39 POSS-Tpy-Eu asap.pdf

Solo gestori archvio

Descrizione: articolo principale
Tipologia: Versione Editoriale
Dimensione 1.32 MB
Formato Adobe PDF
1.32 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
ChemPlusChem-POSS_IRIS.pdf

accesso aperto

Tipologia: Pre-print
Dimensione 924.48 kB
Formato Adobe PDF
924.48 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/426650
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 4
social impact