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Near-infrared (NIR) emissive probes are becoming increasingly popular in biological sensing and imaging due to the advantages of non-invasiveness and deep tissue-penetrating ability. Herein, a series of complexes of trivalent lanthanide ions (Ln = Yb, Er, and Gd) with the commercially available azo dye chromophore 2R (NaHC2R) as ligand and featuring respectively HO and dimethylsulfoxide (DMSO) as ancillary ligands have been prepared. Formulated as [Ln(HC2R)(HO)]·8HO (1-3, Ln = Yb, Er, Gd) and [Ln(HC2R)(DMSO)]·2DMSO (4-6, Ln = Yb, Er, Gd), their structures have been determined by single-crystal X-ray diffraction studies. Photophysical property studies revealed NIR emissions of the DMSO complexes characteristic of Yb(III) and Er(III), effectively sensitized by the dye ligand arising mainly from the π-π* transition of the chromophore. The long-wavelength excitation of the complexes, covering the whole visible-light range and extending into the NIR region, portends the potential applications of such complexes for flexible bioimaging and sensing.
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http://dx.doi.org/10.1039/d4dt00577e | DOI Listing |
Dalton Trans
September 2025
University of Cologne, Faculty for Mathematics and Natural Sciences, Department of Chemistry and Biochemistry, Institute for Inorganic and Materials Chemistry, Greinstrasse 6, D-50939 Köln, Germany.
In the frame of our research aiming to develop efficient triplet-emitting materials, we are exploring the role of the second coordination sphere in enhancing the rigidity of structures and its controlling aspect over the extents of excited state distortions. We thus synthesised three N^C^N cyclometalated complexes [M(L)Cl] (M = Pt, Pd, and Ni), where the two -positions of the pyridyl moieties in 1,3-di(2-pyridyl)-benzene are benzyl substituted (Bn) forming a tight binding pocket for the metal and the Cl ancillary ligand. The molecular structures from single-crystal X-ray diffraction show a markedly distorted square planar M(II) coordination with values of around 0.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
School of Chemistry and Chemical Engineering, International School for Optoelectronic Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.
Organic donor-acceptor-donor (D-A-D) fluorophores with emission in the second near-infrared (NIR-II) window have attracted growing attention for bioimaging applications. While incorporating strong electron donor and acceptor units into the molecular framework enables long-wavelength emission, it inevitably leads to a decrease in the fluorescence quantum efficiency (FQE). Herein, we investigated the microscopic mechanism underlying luminescent efficiency enhancement in NIR-II chromophores featuring asymmetric D-A-D' molecular architectures.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Tianjin Key Laboratory of Chemical Process Safety, Hebei Key Laboratory of Functional Polymers, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin, 300401, P. R. China.
Achieving multi-color tunable time-dependent afterglow color (TDAC) in pure organic materials under visible light excitation remains a significant challenge. Herein, TDAC composites (CDs/U) are prepared with multi-color tunability upon visible-light excitation. Furthermore, the TDAC mechanism is the coexistence of shorter-lived afterglow and longer-lived afterglow.
View Article and Find Full Text PDFPhys Rev E
July 2025
Institute for Basic Science, Center for Theoretical Physics of Complex Systems, (IBS), Daejeon 34126, Korea.
The observation of the Fermi-Pasta-Ulam-Tsingou (FPUT) paradox, namely the lack of equipartition in the evolution of a normal mode in a nonlinear chain on unexpectedly long times, is arguably the most famous numerical experiment in the history of physics. Seventy years after the original publication, most studies in FPUT chains still focus on long wavelength initial states similar to the original paper. It is shown here that all characteristic features of the FPUT paradox are rendered even more striking if modes with short(er) wavelengths are evolved instead.
View Article and Find Full Text PDFBroadband near-infrared (NIR) phosphors have emerged as essential components for next-generation portable and intelligent NIR lights. Nevertheless, the concurrent realization of long-wavelength emission (LWE), wide bandwidth, and high performance remains challenging. Herein, a combined strategy of engineering crystal field and assembling Cr ion pairs within ZnMgAlO spinel solid solutions synergistically induces the evolution of Cr emission from sharp red ( = 709 nm, bandwidth = 24 nm) to broadband NIR region ( = 890 nm, bandwidth = 283 nm).
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