Fluorescence quenching of the N-methylquinolinium cation by pairs of water or alcohol molecules
| Autor: | Carlos Costa Corbelle, M. Carmen Ríos Rodríguez, Berta Fernández, Manuel Mosquera, Flor Rodríguez-Prieto, Jorge A. Pedro |
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| Přispěvatelé: | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares, Universidade de Santiago de Compostela. Departamento de Química Física |
| Rok vydání: | 2017 |
| Předmět: |
Quenching (fluorescence)
Chemistry General Physics and Astronomy 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology Photochemistry 01 natural sciences Fluorescence 0104 chemical sciences Electron transfer Excited state Molecule Photosensitizer Singlet state Physical and Theoretical Chemistry Ionization energy 0210 nano-technology |
| Zdroj: | Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela instname |
| ISSN: | 1463-9084 |
| Popis: | This is the peer-reviewed version of the following article: Physical Chemistry Chemical Physics 2018, 20, 307–316. DOI: 10.1039/C7CP07057H, which has been published in final form at http://pubs.rsc.org/en/content/articlelanding/2017/cp/c7cp07057h. This article may be used for non-commercial purposes only N-Methylquinolinium cation (MQ+) in its first-excited singlet state is a strong oxidant commonly used as a photosensitizer, whose fluorescence is therefore quenched by electron donors. Interestingly, the fluorescence of MQ+ is also quenched by hydroxy compounds such as water and alcohols, more difficult to oxidize. We investigated the quenching mechanism of MQ+ fluorescence by small amounts of water and alcohols in acetonitrile solution. The fluorescence intensities and lifetimes exhibited a nonlinear dependence on the quencher concentration. We found evidence that emissive exciplexes MQ+*-ROH are formed between the excited quinolinium and the hydroxy compounds. An accurate quantitative description of the results was obtained with a model in which the exciplex reacts with a second molecule of the hydroxy compound, which quenches the fluorescence. The rate constant of this process increased as the quencher ionization energy decreased. We showed also that a low basicity of the hydroxy compound inhibits the quenching process. These results are consistent with the existence of a concerted photoinduced proton-coupled electron transfer (PCET) involving an intermediate complex of the excited quinolinium with a H-bonded molecular pair of the hydroxy compounds. In these pairs, a water or an alcohol molecule is able to donate an electron to the photoexcited quinolinium cation and a proton to the second H-bonded hydroxy molecule, showing an enhanced reducing power in comparison with the isolated molecule. The structure of the intermediate complex was investigated using high-level quantum mechanical calculations. At high water concentrations in acetonitrile/water mixtures, the quenching process is slowed down, indicating that higher water aggregates are less effective for a PCET process. The results obtained may be relevant to the study of water oxidation and electron transfer in biological systems This work has received financial support from Gobierno de España, Ministerio de Economía y Competitividad (Grant CTQ2014‐59020‐R), Xunta de Galicia (Grants ED431B 2016/024, ED431D R2016/007, ED431C 2017/17 and Centro Singular de Investigación de Galicia Accreditation 2016‐2019, ED431G/09), and the European Union (European Regional Development Fund ‐ ERDF). Fellowships from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brasil (J.A.P.) and Xunta de Galicia, Spain (C.C.C.) are gratefully acknowledged SI |
| Databáze: | OpenAIRE |
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