Lanthanide luminescence, while ideal for in vivo applications owing to sharp emission bands within the optical window, requires high-intensity, short-wavelength excitation of small organic "antenna" chromophores in the vicinity of the lanthanide complex to access excited f-orbital states through intersystem crossing. Herein, we explored Cherenkov radiation of the radioisotopes F and Zr as an in situ source of antenna excitation. The effective inter- and intramolecular excitation of the terbium(III) complexes of a macrocylic polyaminocarboxylate ligand (hydration number (q)=0, quantum yield (φ)=47 %) as well as its analogue functionalized to append an intramolecular Cherenkov excitation source (q=0.07, φ=63 %) was achieved. Using conventional small-animal fluorescence imaging equipment, we have determined a detection limit of 2.5 nmol of Tb(III) complex in presence of 10 μCi of F or Zr. Our system is the first demonstration of the optical imaging of discrete luminescent lanthanide complexes without external short-wave excitation.
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http://dx.doi.org/10.1002/anie.201809783 | DOI Listing |
J Am Chem Soc
December 2024
Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
Discrete molecular organometallic europium(II) complexes are promising functional materials due to their ability to behave as highly sensitive band-shift luminescence thermometers. Furthering our understanding of the design principles salient to the emission behavior of such systems is important for developing them in this emerging application. To this end, a series of pseudo--symmetric organometallic europium(II) complexes bearing systematically varying ligand sets were synthesized and characterized to probe the influence of subtle structural modification on their optical properties.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Univ Brest, UMR CNRS 6521-, Laboratoire CEMCA, F 29200, Brest, France.
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.
View Article and Find Full Text PDFACS Nano
December 2024
MOE Key Laboratory for Analytical Science of Food Safety and Biology, College of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, China.
Gold nanoclusters (AuNCs) are emerging as promising functional probes for bioapplications. However, because of rapid renal clearance, it is a challenge to tailor their biofate and improve their disease-targeting ability in vivo. Herein, we report an efficient strategy to tailor their organotropic actions by rationally designing AuNC assemblies.
View Article and Find Full Text PDFNanoscale
December 2024
Translational Pharmaceutical Laboratory, Jining First People's Hospital, Shandong First Medical University, Jining 272000, China.
Au(SG) (SG: glutathione) nanoclusters, characterized by their atomically precise structures, exhibit near-infrared II (NIR-II) fluorescence emission and excellent biocompatibility, making them highly promising for imaging applications. However, their comparatively low photoluminescence quantum yield (QY) in aqueous solutions limits their further development. In this study, taking advantage of the molecular-like properties of Au(SG) nanoclusters, we employ a Schiff base reaction to improve their NIR-II emission for the first time.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, CAS-HKU Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry, School of Future Technology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, 100190, China.
The bottom-up synthesis of discrete tubular molecules that mimic the structural features of carbon nanotubes has been a long-standing pursuit for synthetic chemists. As the shortest segments of armchair-type carbon nanotubes, cycloparaphenylenes are regarded as ideal macrocyclic building blocks for achieving this goal. Here we report the synthesis of a helical tubular molecule featuring three diyne linkers between two site-specifically functionalized [9]cycloparaphenylenes.
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