A new tetranuclear compound containing Ru(II) and Ir(III) polypyridine subunits exhibits two independent emissions at room temperature, as a consequence of weak interchromophoric coupling; in contrast, at 77 K energy transfer from Ir-based chromophores to the Ru-based ones is quantitative.
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http://dx.doi.org/10.1039/b508063k | DOI Listing |
Commun Biol
October 2024
State Key Laboratory of Membrane Biology, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, 100084, Beijing, China.
ACS Appl Mater Interfaces
September 2024
College of Chemistry, Chemical Engineering and Environment, Fujian Provincial Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou, Fujian 363000, PR China.
Room-temperature phosphorescent carbon dots (RTP-CDs) have received increasing attention due to their excellent optical properties and potential applications. Nevertheless, the realization of RTP-CDs in aqueous solutions remains a considerable challenge due to the water-molecule- and oxygen-induced deactivation of the triplet excitons, which leads to phosphorescence quenching. In this study, ultralong phosphorescence in water was achieved by in situ self-assembly of CDs encapsulated in a rigid hydrogen-bonded organic framework (HOF).
View Article and Find Full Text PDFChem Commun (Camb)
August 2024
College of Chemistry and Chemical Engineering, Chongqing University, Chongqing, PR China.
This research presents a new approach to create two-color luminescent physically unclonable functions (PUFs) using an organic luminophore with tunable emission colors. These PUFs offer high security and stable performance, significantly enhancing anti-counterfeiting capabilities by exponentially increasing encoding capacity through dual-color integration and complex pattern formation.
View Article and Find Full Text PDFCytometry A
August 2024
Morgridge Institute for Research, Madison, Wisconsin, USA.
Autofluorescence lifetime imaging microscopy (FLIM) is sensitive to metabolic changes in single cells based on changes in the protein-binding activities of the metabolic co-enzymes NAD(P)H. However, FLIM typically relies on time-correlated single-photon counting (TCSPC) detection electronics on laser-scanning microscopes, which are expensive, low-throughput, and require substantial post-processing time for cell segmentation and analysis. Here, we present a fluorescence lifetime-sensitive flow cytometer that offers the same TCSPC temporal resolution in a flow geometry, with low-cost single-photon excitation sources, a throughput of tens of cells per second, and real-time single-cell analysis.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences (MPI-NAT), Am Fassberg 11, 37077, Göttingen, Germany.
New photostable and bright supramolecular complexes based on cucurbit[7]uril (CB7) host and diketopyrrolopyrole (DPP) guest dyes having two positively charged 4-(trimethylammonio)phenyl groups were prepared and characterized. The dye core displays large Stokes shift (in HO, abs./emission max.
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