Publications by authors named "C Latouche"

We report the synthesis and characterization of two chiral binuclear iridium(III) complexes ( and ) prepared from enantiopure building blocks [μ-Cl(Δ-Ir(C^N))] and [μ-Cl(Λ-Ir(C^N))]. These building blocks have been obtained by chiral preparative high-performance liquid chromatography of the neutral iridium(III) complex (piv = 2,2,6,6-tetramethylheptane-3,5-dionate) followed by selective degradation of the ancillary ligand. For comparison purposes, we also synthesized a monomer () and a dimer (, mixture).

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Hybrid copper(I) halide materials are currently attracting significant attention due to their exceptional luminescence properties, offering great potential for the development of multifunctional emissive materials with, in addition, eco-friendly features. A binuclear copper iodide complex, based on the [CuIL] motif with phosphite derivatives as ligands, has been synthesized and structurally characterized. Photophysical investigations indicate that this complex displays luminescence thermochromic properties, which are characterized by a temperature-dependent change in the relative intensity of two emission bands.

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Article Synopsis
  • A copper(I) complex in a supercooled liquid state changes into a crystalline phase when mechanically stimulated.
  • This transformation results in a significant color change in its emission from red to green.
  • The photoluminescence quantum yield increases 20 times to 87%, and this phase change is reversible due to the complex's ability to create a supercooled metastable state.
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We report the synthesis and characterization of ten neutral bisheteroleptic iridium(III) complexes with 2-phenylbenzimidazole cyclometallating ligand and picolinate as ancillary ligand. The 2-phenylbenzimidazole has been modified by selected substituents introduced on the cyclometallating ring and/or on the benzimidazole moiety. The integrity of the complexes has been assessed by NMR spectroscopy, by high-resolution mass spectrometry and by elemental analysis.

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Article Synopsis
  • Sodium dependent multivitamin transporter (SMVT) deficiency is a rare genetic disorder that causes health issues due to a lack of certain vitamins, affecting around 10 known families.
  • This study introduced 4 new patients from Algeria, all sharing a specific genetic mutation related to SMVT, confirming its harmful effects through RNA analysis.
  • The patients exhibited similar symptoms, including optic atrophy, severe vomiting, and rapid neurological decline, suggesting a common genetic background due to a "founder effect."
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