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Fluorescent Zr(IV) Metal-Organic Frameworks Based on an Excited-State Intramolecular Proton Transfer-Type Ligand.
Trannoy, Virgile; Guillou, Nathalie; Livage, Carine; Roch-Marchal, Catherine; Haouas, Mohamed; Léaustic, Anne; Allain, Clémence; Clavier, Gilles; Yu, Pei; Devic, Thomas.
Afiliación
  • Trannoy V; ILV , Université de Versailles St Quentin, UMR CNRS 8180, Université Paris-Saclay, 78035 Versailles , France.
  • Guillou N; ICMMO , Université Paris-Sud , UMR CNRS 8182, Université Paris-Saclay, 91405 Orsay Cedex , France.
  • Livage C; PPSM , ENS Paris-Saclay, UMR CNRS 8531, Université Paris-Saclay, 94235 Cachan , France.
  • Roch-Marchal C; ILV , Université de Versailles St Quentin, UMR CNRS 8180, Université Paris-Saclay, 78035 Versailles , France.
  • Haouas M; ILV , Université de Versailles St Quentin, UMR CNRS 8180, Université Paris-Saclay, 78035 Versailles , France.
  • Léaustic A; ILV , Université de Versailles St Quentin, UMR CNRS 8180, Université Paris-Saclay, 78035 Versailles , France.
  • Allain C; ILV , Université de Versailles St Quentin, UMR CNRS 8180, Université Paris-Saclay, 78035 Versailles , France.
  • Clavier G; ICMMO , Université Paris-Sud , UMR CNRS 8182, Université Paris-Saclay, 91405 Orsay Cedex , France.
  • Yu P; PPSM , ENS Paris-Saclay, UMR CNRS 8531, Université Paris-Saclay, 94235 Cachan , France.
  • Devic T; PPSM , ENS Paris-Saclay, UMR CNRS 8531, Université Paris-Saclay, 94235 Cachan , France.
Inorg Chem ; 58(10): 6918-6926, 2019 May 20.
Article en En | MEDLINE | ID: mdl-31070359
We report here the preparation of a series of Zr(IV) metal-organic frameworks (MOFs) of the MIL-140 structure type incorporating a ligand exhibiting an intense excited-state intramolecular proton transfer (ESIPT) fluorescence. These solids were obtained by systematically varying the substitution rate of 4,4'-biphenyldicarboxylate by 2,2'-bipyridine-3,3'-diol-5,5'-dicarboxylate, and they were thoroughly characterized by complementary techniques, including high-resolution powder X-ray diffraction, solid-state NMR spectroscopy, nitrogen sorption experiments, and time-resolved fluorescence. We show that the incorporation of the ESIPT-type ligand induces an increase of the hydrophilicity, leading ultimately to a higher sensitivity toward hydrolysis, a phenomenon rarely observed in this structure type, which is considered as one of the most stable among the Zr carboxylate MOFs. Eventually, optimization of the amount of fluorescent ligand within the structure allowed combining a decent microposity ( SBET > 750 m2·g-1) and a high stability even in boiling water, together with a high fluorescence quantum yield (>30%).

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos