Aromatic fluorine atom-induced highly amine-sensitive trimethine cyanine dye showing colorimetric and ratiometric fluorescence change.
Ryunosuke KaniYasuhiro KubotaToshiyasu InuzukaKazumasa FunabikiPublished in: RSC advances (2022)
Herein, introducing multiple fluorine atoms into aromatic rings of trimethine cyanine dyes is proposed as a powerful method for dramatically increasing sensitivity to amines. The highly sensitive ratiometric fluorescence properties previously available only by intramolecular addition can be exploited in reactions with intermolecular amines or other nucleophiles.
Keyphrases
- energy transfer
- fluorescent probe
- living cells
- quantum dots
- positron emission tomography
- single molecule
- aqueous solution
- sensitive detection
- amino acid
- pet imaging
- gold nanoparticles
- high glucose
- diabetic rats
- hydrogen peroxide
- computed tomography
- molecular dynamics
- drug induced
- endothelial cells
- nitric oxide
- pet ct
- electron transfer
- high resolution
- tandem mass spectrometry