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Luminescent lanthanide complexes can exhibit temperature-sensitive metal-centered emission due to energy transfer quenching from the lanthanide to the ligand triplet states, which have been promising application in emission lifetime-based thermometers. However, the long-lived ligand triplet state limits the temperature sensitivity of lanthanide emission. This study demonstrates an enhancement in the temperature sensitivity of Tb(III) emission by introducing an energy escape pathway from the ligand triplet state. A dinuclear Tb(III)-Nd(III) complex containing hexafluoroacetylacetonate (hfa) and triphenylene bridging ligands was prepared, which exhibits temperature-dependent energy transfer from the Tb(III)-emitting state to the hfa triplet state. The triplet level of the hfa ligand is similar to that of the triphenylene ligand, inducing effective energy transfer from hfa to Nd(III) via the triphenylene ligands. This energy transfer pathway provides a short-lived excited state of hfa ligands, resulting in the highest temperature sensitivity (4.4% K) among emission lifetime-based thermometers of lanthanide complexes.
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http://dx.doi.org/10.1038/s42004-025-01673-1 | DOI Listing |
Anal Sens
January 2025
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390 United States.
At present, two competing hyperpolarization (HP) techniques, dissolution dynamic nuclear polarization (DNP) and parahydrogen (para-H) induced polarization (PHIP), can generate sufficiently high liquid state C signal enhancement for in vivo studies. PHIP utilizes the singlet spin state of para-H to create non-equilibrium spin populations. In hydrogenative PHIP, para-H is irreversibly added to unsaturated precursors, typically in the presence of a homogeneous catalyst.
View Article and Find Full Text PDFChem Sci
August 2025
Inorganic and Organometallic Chemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg Egerlandstraße 1 91058 Erlangen Germany
Mechanochemical reduction of β-diketiminate (BDI) barium iodide precursors with K/KI resulted in the first barium inverse sandwich complexes containing the benzene dianion in yields of up to 54%. This most challenging isolation of highly reactive (BDI)Ba-(CH)-Ba(BDI) complexes, completes the family of heavier benzene inverse sandwich complexes and allows for a comparison of trends in the series from Mg, Ca, Sr to Ba. Syntheses, stabilities, structures, electronic states and reactivities of the full range are compared.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, United States.
We report the first paramagnetic boron tetraradical, comprising four boraphenanthrene-type units with boryl radical centers bridged by a central tetraphenylethene (TPE) linker. With strongly π-accepting and sterically demanding cyclic(alkyl)(amino) carbene ligands (), spin densities localize on the boron-carbene fragments (92%), consistent with a true boron-centered tetraradical. Magnetic measurements of reveal minimal spin-spin coupling, consistent with four noninteracting = 1/2 centers.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, Yunnan 650500, China; Southwest United Graduate School, Kunming 650092, China.
Microbial-derived extracellular polymeric substances (EPS) and iron minerals are ubiquitous in aquatic environments, and they can influence the fate of organic micropollutants such as 17α-ethinylestradiol (EE2). However, the interactions between EPS and iron minerals, and their influence on EE2 photodegradation, are seldom addressed in the literature. This study explored the effects of EPS derived from different aerobic or anaerobic microbials on the reductive dissolution of ferrihydrite (Fhy) and subsequent EE2 photodegradation, with emphasis on the impact of Fe-EPS complexes formation.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Applied Chemistry for Environment, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen-Uegahara, Sanda, Hyogo, 669-1330, Japan.
A series of mixed metal crystals comprising square-planar platinum(II) and palladium(II) complexes, K[M(CN)(dFppy)]·HO (M = Pt, Pd; dFppy = 2-(4,6-difluorophenyl)pyridinate), were prepared, and their unique luminescence properties-emerging upon mixing-were revealed. Seven mixed crystals with Pt/Pd ratios of 1:0.5, 1:1, 1:1.
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