Fluorescence quenching and electron transfer in water-soluble copolymers of methacrylic acid and vinylperylene or N-[10-(4-aminonaphthalimide)]-2-methylacrylamide

1988 ◽  
Vol 92 (23) ◽  
pp. 6625-6630 ◽  
Author(s):  
R. D. Stramel ◽  
S. E. Webber ◽  
M. A. J. Rodgers
Keyword(s):  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Methacrylic Acid ◽  
Water Soluble

The photo-initiation of the polymerization of vinyl compounds by means of cerous ions

1963 ◽  
Vol 275 (1361) ◽  
pp. 161-174 ◽  
Keyword(s):  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Methacrylic Acid ◽  
Polymerization Reaction ◽  
Hydrogen Ions ◽  
Transfer Processes ◽  
Flash Technique ◽  
Electron Transfer Processes ◽  
Kinetics Of

The kinetics of the polymerization of acrylonitrile and methacrylic acid photosensitized by cerous ions have been studied. Cerous salts have been photolyzed in different media by means of the flash technique and ceric ions were produced, accompanied by fluorescence. Quenching of the fluorescence of the excited ceric species has been investigated with and without the presence of monomer and it has been demonstrated that hydrogen ions are necessary for the polymerization reaction to proceed. The results are consistent with the following electron transfer processes: Ce 3+ . HOH + hv ^+ (Ce 4+ . HOH - )*, Ce 4+ . HOH - )* hv ^+ Ce 3+ . HOH+ hv ", Ce 4+ . HOH - )* +H + ->Ce 4+ . H 2 O+H', Ce 4+ . HOH - )* +H + + M ->Ce 4+ +H 2 M H', where M = monomer.

Using Quenching Kinetics and Thermodynamics of Amino-Fluorophores as Empirical Tools for Predicting Boronic Acid Sensors Suitable for Use in Physiological Conditions

2011 ◽  
Vol 64 (11) ◽  
pp. 1438 ◽  
Author(s):  
Nicholas McGregor ◽  
Christophe Pardin ◽  
W. G. Skene
Keyword(s):  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Boronic Acid ◽  
Sulfonic Acid ◽  
Phenylboronic Acid ◽  
Water Soluble ◽  
Time Resolved ◽  
Diffusion Limited ◽  
Phenylboronic Acids ◽  
Acid Sensors

A series of water-soluble 1-amino-naphthalenes and 2-amino-fluorenes are prepared. These serve as model fluorophores for measuring the thermodynamics and kinetics of fluorescence quenching with phenylboronic acids and aliphatic amines. Steady-state and time-resolved fluorescence quenching kinetics are investigated using the Stern–Volmer method. Diffusion limited quenching constants and exergonic thermodynamics of electron transfer are derived for the 5-amino-1-napthol and 2-aminofluorene derivatives with phenylboronic acid and/or an aliphatic imine. No quenching and endergonic thermodynamics or electron transfer are observed for 5-sulfonamide, 5-sulfonic acid, or 5-hydroxy-7-sulfonic acid aminonaphthalene derivatives. Boronic acid sensors synthesized from these aminofluorophores by reductive amination with 2-formylphenylboronic acid undergo fluorescence revival in the presence of saccharides only when the fluorophore demonstrates diffusion limited quenching kinetics and exergonic thermodynamics of electron transfer with the boronic acid or imine quenchers. Thus, these two properties are suitable empirical tools for predicting saccharide-induced fluorescence revival of boronic acid sensors.

Formation of CT complexes and electron transfer from excited molecules of anthracene derivatives to methylviologen in aqueous and micellar media

1987 ◽  
Vol 52 (7) ◽  
pp. 1658-1665
Author(s):  
Viktor Řehák ◽  
Jana Boledovičová
Keyword(s):  
Electron Transfer ◽  
Complex Formation ◽  
Fluorescence Quenching ◽  
Rate Constant ◽  
Formation Constants ◽  
Dynamic Quenching ◽  
Micellar Media ◽  
Complex Formation Constants ◽  
Anthracene Derivatives ◽  
Ct Complexes

Disodium 1,5- and 1,8-anthracenedisulphonate (ADS) and 9-acetylanthracene form coloured CT complexes with methylviologen (MV2+) in aqueous and micellar media. The complex formation constants and molar absorptivities were determined by the Benesi-Hildebrandt method. In the fluorescence quenching, its static component plays the major role. The dynamic quenching component is determined by the rate constant of electron transfer from the S1 state of ADS to MV2+.

Fluoreszenzlöschung alternierender und nicht-alternierender polycyclischer aromatischer Kohlenwasserstoffe durch Nitroverbindungen / Fluorescence Quenching of Alternant and Non-alternant Polycyclic Hydrocarbons by Nitro Compounds

1977 ◽  
Vol 32 (12) ◽  
pp. 1561-1563 ◽  
Author(s):  
M. Zander
Keyword(s):  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Excitation Energy ◽  
Reduction Potential ◽  
Nitro Compounds ◽  
Polycyclic Hydrocarbons ◽  
Electron Transfer Mechanism ◽  
Diffusion Controlled ◽  
Polycyclic Aromatic ◽  
Alternant Hydrocarbons

Abstract Fluorescence Quenching of Alternant and Non-alternant Polycyclic Hydrocarbons by Nitro Compounds Fluorescence quenching of polycyclic aromatic hydro­ carbons by nitromethane or nitrobenzene in fluid solutions is due to an electron transfer mechanism. The non diffusion controlled rate constant of quenching is very much greater for alternant than for non-alternant hydrocarbons with equal singlet excitation energy. This is explained by the known more positive reduction potential of non-alternant compared to alternant hydrocarbons.

Fluorescence quenching of aromatic molecules by SCN− in acetonitrile: effect of molecular size on electron transfer fluorescence quenching

1997 ◽  
Vol 276 (3-4) ◽  
pp. 210-216 ◽  
Author(s):  
Chika Sato ◽  
Koichi Kikuchi ◽  
Hiromi Ishikawa ◽  
Makio Iwahashi ◽  
Hiroshi Ikeda ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Molecular Size ◽  
Aromatic Molecules

Photoinduced electron transfer between quantum dots and pralidoxime: an efficient sensing strategy

2017 ◽  
Vol 41 (19) ◽  
pp. 10828-10834 ◽  
Author(s):  
A. R. Jose ◽  
A. E. Vikraman ◽  
K. Girish Kumar
Keyword(s):  
Quantum Dots ◽  
Electron Transfer ◽  
Fluorescence Quenching ◽  
Photoinduced Electron Transfer ◽  
Cds Quantum Dots

Photoinduced electron transfer (PET)-mediated fluorescence quenching of CdTe/CdS quantum dots by pralidoxime (PAM).

Sign in / Sign up

Export Citation Format

Share Document