2021
DOI: 10.1016/j.ccr.2020.213712
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Design strategy and recent progress of fluorescent probe for noble metal ions (Ag, Au, Pd, and Pt)

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Cited by 60 publications
(21 citation statements)
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“…The palladium could subsequently bind with thiol-containing proteins, nucleic acids and other biomacromolecules to disturb their normal physiological function and endanger human health. 161–163 Therefore, the residual palladium concentration in the environment needs to be detected in real time. Lin's group synthesized a propargyl ether decorated hemicyanine fluorophore NIR-Pd-1 for monitoring palladium (Fig.…”
Section: Nir Fluorescent Probes For Ionic Speciesmentioning
confidence: 99%
“…The palladium could subsequently bind with thiol-containing proteins, nucleic acids and other biomacromolecules to disturb their normal physiological function and endanger human health. 161–163 Therefore, the residual palladium concentration in the environment needs to be detected in real time. Lin's group synthesized a propargyl ether decorated hemicyanine fluorophore NIR-Pd-1 for monitoring palladium (Fig.…”
Section: Nir Fluorescent Probes For Ionic Speciesmentioning
confidence: 99%
“…by virtue of their strong coordinating abilities with electronegative heteroatoms (N, O, S, etc. ). ,, Common principles available for this purpose are based on (1) suitable ring/cavity size for a prescribed ions, such as crown ethers with various ring sizes for alkali and alkaline earth metal ions; (2) applicable ligands for easily generation of five- or six-membered ring complexes with metal ions, such as ethylene glycol tetraacetic acid moiety for Ca 2+ ; and (3) soft/hard acid base theory, such as the soft sulfur-containing receptors with high affinity for soft metal ions (e.g., Hg 2+ ). On the other hand, for design of such probes, a photophysical process, like PET, and ICT should be incorporated to translate analytes binding into a spectroscopic signal change.…”
Section: Activatable Pa Probes For Molecular Detectionmentioning
confidence: 99%
“…Inspired by the pioneering work of Alexander L. Antaris et al, certain building blocks have created NIR-II fluorophores. [17] One of the most common methods include exploiting benzo[1,2-c:4,5-c']bis( [1,2,5]thiadiazole) (BBTD) as an electron acceptor core attached to thiophene, triphenylamine, and their derivatives. In addition, upon binding with the aryl group, the cyano group could induce intermolecular electron transfer to ensure the emission of NIR-II fluorescence.…”
Section: D-a Systemmentioning
confidence: 99%
“…[1][2][3] Among numerous imaging methods, fluorescence-based imaging methods enable scientists to uniquely visualize and interpret biological events, which act as a direct, easy-operative, and noninvasive approach for studying life sciences. [4][5][6] Conventional fluorescence imaging methods exploit fluorescence in the visible (400-650 nm) and the first near-infrared window (NIR-I) regions (650−950 nm), which exhibit defects of relatively low tissue penetration, unavoidable tissue absorption and scattering, and undesired autofluorescence that deteriorate the imaging efficacy. [7][8][9] Thus, to reduce these adverse factors, fluorescence imaging in the second near-infrared (NIR-II) region (1000-1700 nm)…”
Section: Introductionmentioning
confidence: 99%