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- W4246202785 endingPage "6306" @default.
- W4246202785 startingPage "6295" @default.
- W4246202785 abstract "Abstract Polymethine cyanine dyes have been widely recognized as promising chemical tools for a range of life science and biomedical applications, such as fluorescent staining of DNA and proteins in gel electrophoresis, fluorescence guided surgery, or as ratiometric probes for probing biochemical pathways. The photophysical properties of such dyes can be tuned through the synthetic modification of the conjugated backbone, for example, by altering aromatic cores or by varying the length of the conjugated polymethine chain. Alternative routes to shaping the absorption, emission, and photostability of dyes of this family are centered around the chemical modifications on the polymethine chain. This Minireview aims to discuss strategies for the introduction of substituents in the meso‐position, their effect on the photophysical properties of these dyes and some structure–activity correlations which could help overcome common limitations in the state of the art in the synthesis." @default.
- W4246202785 created "2022-05-12" @default.
- W4246202785 creator A5018800747 @default.
- W4246202785 creator A5065729610 @default.
- W4246202785 creator A5086142941 @default.
- W4246202785 date "2020-12-28" @default.
- W4246202785 modified "2023-10-14" @default.
- W4246202785 title "Explorations into the Effect of <i>meso</i> ‐Substituents in Tricarbocyanine Dyes: A Path to Diverse Biomolecular Probes and Materials" @default.
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