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• W2904433239 endingPage "989" @default.
• W2904433239 startingPage "981" @default.
• W2904433239 abstract "Spectral stability of small-molecule fluorescent probes is required for correct interpretation and reproducibility of multicolor fluorescence imaging data, in particular under high (de)excitation light intensities of super-resolution imaging or in single-molecule applications. We propose a synthetic approach to a series of spectrally stable rhodamine fluorophores based on sequential Ru- and Cu-catalyzed transformations, evaluate their stability against photobleaching and photoconversion in the context of other fluorophores using chemometric analysis, and demonstrate chemical reactivity of fluorophore photoproducts. The substitution patterns providing the photoconversion-resistant triarylmethane fluorophores have been identified, and the applicability of nonbluing labels in live-cell STED nanoscopy is demonstrated." @default.
• W2904433239 created "2018-12-22" @default.
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• W2904433239 date "2018-12-18" @default.
• W2904433239 modified "2023-10-17" @default.
• W2904433239 title "Triarylmethane Fluorophores Resistant to Oxidative Photobluing" @default.
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• W2904433239 doi "https://doi.org/10.1021/jacs.8b11036" @default.
• W2904433239 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6728092" @default.
• W2904433239 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30562459" @default.
• W2904433239 hasPublicationYear "2018" @default.
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