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PubMed Publications| Keyword search (4,164 papers available) |  |
"Richezzi M" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Photoluminescent Properties of Tb-UiO-66 Metal-Organic Framework Analogues | Canales Gálvez XA; Richezzi M; Bicalho HA; Labadie N; Pellegrinet SC; Titi HM; Howarth AJ; | 39849977 CNSR |
| 2 | Rare-earth acetates as alternative precursors for rare-earth cluster-based metal-organic frameworks | Richezzi M; Donnarumma PR; Copeman C; Howarth AJ; | 38646995 CNSR |
| Title: | Photoluminescent Properties of Tb-UiO-66 Metal-Organic Framework Analogues | ||||
| Authors: | Canales Gálvez XA, Richezzi M, Bicalho HA, Labadie N, Pellegrinet SC, Titi HM, Howarth AJ | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/39849977/ | ||||
| DOI: | 10.1021/acs.inorgchem.4c04523 | ||||
| Publication: | Inorganic chemistry | ||||
| Keywords: | |||||
| PMID: | 39849977 | Category: | Date Added: | 2025-01-24 | |
| Dept Affiliation: |
CNSR
1 Department of Chemistry and Biochemistry and Centre for NanoScience Research, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec H4B 1R6, Canada. 2 Instituto de Química Rosario (CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, Rosario, Santa Fe 2000, Argentina. 3 Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec H3A 0B8, Canada. |
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Description: |
Three new analogues of Tb-UiO-66 with various functional groups (-F, -Br, -NH2) on the terephthalic acid linker of the metal-organic framework (MOF) are synthesized and characterized. The photoluminescent properties of these analogues, as well as Tb-UiO-66 and Tb-UiO-66-(OH)2, are studied and correlated to the calculated energies for the triplet (T1) states of each linker. The results show that the addition of electron withdrawing groups, such as -F and -Br, lead to higher T1 energies, resulting in quantum yields in the range of 6-31%. The addition of electron donating groups, on the other hand, lowers the T1 energy of the organic linker and inhibits energy transfer such that emission is not observed. |
