Literature DB >> 14872232

Quenching of the fluorescence of pterin derivatives by anions.

Carolina Lorente1, Alberto L Capparelli, Andrés H Thomas, André M Braun, Esther Oliveros.   

Abstract

Steady-state and time-resolved studies of the fluorescence of pterins in aqueous solutions in the presence of different anions have been performed using the single-photon counting technique. In the pH range between 3 and 13, most pterins exist in a protonated and a deprotonated form. Results obtained for both acid and basic forms of five compounds belonging to the pterin family (pterin, 6-carboxypterin, 6-formylpterin, biopterin and neopterin) show that the fluorescence of the acid forms is dynamically quenched by phosphate and acetate, and the corresponding bimolecular rate constants of fluorescence quenching (k(q)) are reported. These results are of importance from the technical and analytical points of view because measurements of the fluorescence of pterin derivatives for a variety of purposes are often performed in the presence of salts, especially buffers, and significant quenching of the pterin fluorescence by the buffer might lead to errors in interpretation and erroneous conclusions. No quenching of the fluorescence of the acid forms by chloride, sulfate or nitrate was detected. The fluorescence of the basic forms was either not quenched by anions or any such quenching was negligible in comparison with that observed for the acid forms.

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Year:  2003        PMID: 14872232     DOI: 10.1039/b313076b

Source DB:  PubMed          Journal:  Photochem Photobiol Sci        ISSN: 1474-905X            Impact factor:   3.982


  4 in total

1.  Molecular fluorescence, phosphorescence, and chemiluminescence spectrometry.

Authors:  Kristin A Fletcher; Sayo O Fakayode; Mark Lowry; Sheryl A Tucker; Sharon L Neal; Irene W Kimaru; Matthew E McCarroll; Gabor Patonay; Philip B Oldham; Oleksandr Rusin; Robert M Strongin; Isiah M Warner
Journal:  Anal Chem       Date:  2006-06-15       Impact factor: 6.986

2.  Dissociative photoelectron capture as a model for low-energy electron accepting in biochemical reactions.

Authors:  O N Brzhevskaya; E N Degtyarev; T S Zhuravleva; A S Zubkov; I V Klimenko; E M Sheksheev; O S Nedelina
Journal:  Dokl Biochem Biophys       Date:  2008 May-Jun       Impact factor: 0.788

Review 3.  Synthesis, Redox and Spectroscopic Properties of Pterin of Molybdenum Cofactors.

Authors:  Kyle J Colston; Partha Basu
Journal:  Molecules       Date:  2022-05-22       Impact factor: 4.927

4.  Flower-like supramolecular self-assembly of phosphonic acid appended naphthalene diimide and melamine.

Authors:  Rajesh S Bhosale; Mohammad Al Kobaisi; Sidhanath V Bhosale; Suresh Bhargava; Sheshanath V Bhosale
Journal:  Sci Rep       Date:  2015-09-29       Impact factor: 4.379

  4 in total

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