Two-Photon Antenna Sensitization of Curium: Evidencing Metal-Driven Effects on Absorption Cross Section in f-Element Complexes.
Catecholamines
/ chemistry
Coordination Complexes
/ chemistry
Curium
/ chemistry
Electron Transport
Enterobactin
/ chemistry
Europium
/ chemistry
Fluorescein
/ chemistry
Fluorescent Dyes
/ chemistry
Ligands
Molecular Structure
Photons
Pyridones
/ chemistry
Spectrometry, Fluorescence
Terbium
/ chemistry
Journal
The journal of physical chemistry letters
ISSN: 1948-7185
Titre abrégé: J Phys Chem Lett
Pays: United States
ID NLM: 101526034
Informations de publication
Date de publication:
06 Aug 2020
06 Aug 2020
Historique:
pubmed:
9
7
2020
medline:
20
4
2021
entrez:
9
7
2020
Statut:
ppublish
Résumé
Two-photon-excited fluorescence spectroscopy is a powerful tool to study the structural and electronic properties of optically active complexes and molecules. Although numerous lanthanide complexes have been characterized by two-photon-excited fluorescence in solution, this report is the first to apply such a technique to actinide compounds. Contrasting with previous observations in lanthanides, we demonstrate that the two-photon absorption properties of the complexes significantly depend on the metal (4f vs 5f), with Cm(III) complexes showing significantly higher two-photon absorption cross sections than lanthanide analogues and up to 200-fold stronger emission intensities. These results are consistent with electronic and structural differences between the lanthanide and actinide systems studied. Hence, the described methodology can provide valuable insights into the interactions between f-elements and ligands, along with promising prospects on the characterization of scarce compounds.
Identifiants
pubmed: 32635727
doi: 10.1021/acs.jpclett.0c01888
doi:
Substances chimiques
Catecholamines
0
Coordination Complexes
0
Fluorescent Dyes
0
Ligands
0
Pyridones
0
Terbium
06SSF7P179
Enterobactin
28384-96-5
Europium
444W947O8O
Curium
M5LL84MZ2W
Fluorescein
TPY09G7XIR
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM