Publications by authors named "L Charbonniere"

Lanthanide nanoparticles (LnNPs) feature sharp emission lines together with millisecond emission lifetimes which make them promising luminescent probes for biosensing and bioimaging. Although LnNPs are attracting much interest, their photoluminescence properties at the single nanoparticle level remain largely unexplored. Here, we employ fluorescence correlation spectroscopy (FCS) and photoluminescence burst analysis to investigate the photodynamics of Sm- and Eu-based LnNPs with single nanoparticle sensitivity and microsecond resolution.

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Ligands combining two lateral bis-pyridyl-phosphonated-pyclens were synthesized, using a flexible linear pegylated linker (L2) or a bulkier K22 crown-ether (L3). A functionalized pyridyl-phosphonated-pyclen (L1) was also prepared as a mononuclear analogue. Coordination behavior of lanthanide cations was studied via NMR titration with Lu for L1, and UV/Vis and luminescence spectroscopy with Yb for L2/L3.

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Article Synopsis
  • Bispidine chelators are effective for creating stable metal complexes, and this study focuses on developing new terbium(III) complexes for medical imaging using bispidine-based ligands.
  • The two synthesized complexes, differentiated by pyridine-phosphonate and picolinate subunits, exhibit distinct conformations and protonation schemes, affecting their stability and behavior.
  • Notably, one complex shows remarkable kinetic inertness in various environments, retaining stability over extended periods, while also displaying bright luminescence, which is promising for imaging applications.
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The conventional energy transfer pathway in organic lanthanide complexes is purported to be from the excited singlet state of the chromophore to the triplet state and subsequently directly to the emitting state of the trivalent lanthanide ion. In this work, we found that the energy transfer occurs from the triplet state to the nearest energy level, instead of directly to the emitting state of the lanthanide ion. The triplet decay rate for different lanthanide ions follows an energy gap law from the triplet level to the receiving level of the lanthanide ion.

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A series of Tb-doped LaF nanoparticles (NPs) was prepared by systematically varying the Tb doping rate from 0 to 100%. The elemental composition was confirmed by inductively coupled plasma atomic emission spectroscopy (ICP-AES) analysis, and the size, morphology, and crystal structure were determined in the solid state by transmission electron microscopy and X-ray diffractometry, while the size and ζ-potential of the NPs in solution were studied by dynamic light scattering, Taylor dispersion analysis, and laser Doppler electrophoresis. While the crystal structure appears to be hexagonal for a doping rate of up to 70%, an admixture of hexagonal and orthorhombic phases is observed for 80 and 90% Tb contents with a pure orthorhombic phase being obtained for TbF.

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