Electrochromic Modulation of Excited-State Intramolecular Proton Transfer:  The New Principle in Design of Fluorescence Sensors

• Published in: Journal of the American Chemical Society 2002-10, Vol.124 (41), p.12372-12379
• Main Authors: Klymchenko, Andrey S, Demchenko, Alexander P
• Format: Article
• Language: English
• Subjects: Atomic and molecular physics; Electrochemistry; Exact sciences and technology; Flavonoids - chemical synthesis; Flavonoids - chemistry; Fluorescence and phosphorescence spectra; Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion); Fluorescent Dyes - chemical synthesis; Fluorescent Dyes - chemistry; Molecular properties and interactions with photons; Photochemistry; Physics; Protons; Spectrometry, Fluorescence; Static Electricity
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja027669l

Internal Stark effect (or internal electrochromy) consists of the shift of light absorption and emission bands under the influence of electric field produced by proximal charges. In the studies of 3-hydroxyflavone (3HF) derivatives exhibiting the excited-state intramolecular proton transfer (ESIPT), we describe a new phenomenon − a very strong internal electrochromic modulation of this reaction. Fluorescence spectra of 3HF derivatives with charged groups attached to the chromophore from the opposite sides without π-electronic conjugation, N-[(4‘-diethylamino)-3-hydroxy-6-flavonyl]methyl-N,N-dimethyloctylammonium bromide and 4-{4-[4‘-(3-hydroxyflavonyl)]piperazino}-1-(3-sulfopropyl)pyridinium, were compared with those of their neutral analogues in a series of representative solvents. The introduction of the proximal charge results in shifts of absorption spectrum and of both normal (N*) and tautomer (T*) emission bands, which correspond to initial and phototautomer states of the ESIPT reaction. The observed shifts are in accordance with the Stark effect theory. The direction of the shift depends on the position of the proximal charge with respect to the chromophore. The magnitude of the shift depends strongly on the solvent dielectric constant and on screening or unscreening produced by addition of the hydrophobic salts. In all of these cases, the spectral shifts are accompanied by extremely strong variations of relative intensities of N* and T* emission bands. This signifies a strong influence of internal electric field on the ESIPT reaction, which produces a dramatic change of emission color. Thus, the coupling of the initial electrochromic sensory signal with the ESIPT reaction allows for the breaking of the limit in magnitude of response inherent to common electrochromic dyes. This suggests a new principle of designing the ultrasensitive electrochromic two-wavelength fluorescence sensors and probes for analytical chemistry, macromolecular science, and cellular biology.