TDDFT prediction of UV-vis absorption and emission spectra of tocopherols in different media

Verfasser / Beitragende:
[Kahina Bakhouche, Zoubeida Dhaouadi, Souad Lahmar, Dalila Hammoutène]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Modeling, 21/6(2015-06-01), 1-13
Format:
Artikel (online)
ID: 605511020
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024 7 0 |a 10.1007/s00894-015-2706-1  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00894-015-2706-1 
245 0 0 |a TDDFT prediction of UV-vis absorption and emission spectra of tocopherols in different media  |h [Elektronische Daten]  |c [Kahina Bakhouche, Zoubeida Dhaouadi, Souad Lahmar, Dalila Hammoutène] 
520 3 |a We use the TDDFT/PBE0/6-31+G* method to determine the electronic absorption and emission energies, in different media, of the four forms of tocopherol, which differ by the number and the position of methyl groups on the chromanol. Geometries of the ground state S0 and the first singlet excited state S1 were optimized in the gas phase, and various solvents. The solvent effect is evaluated using an implicit solvation model (IEF-PCM). Our results are compared to the experimental ones obtained for the vitamin E content in several vegetable oils. For all forms of tocopherols, the HOMO-LUMO first vertical excitation is a π-π* transition. Gas phase and non-polar solvents (benzene and toluene) give higher absorption wavelengths than polar solvents (acetone, ethanol, methanol, DMSO, and water); this can be interpreted by a coplanarity between the O-H group and the chroman, allowing a better electronic resonance of the oxygen lone pairs and the aromatic ring, and therefore giving an important absorption wavelength, whereas the polar solvents give high emission wavelengths comparatively to gas phase and non-polar solvents. Fluorescence spectra permit the determination, the separation, and the identification of the four forms of tocopherols by a large difference in emission wavelength values. Graphical Abstract Scheme from process methodological to obtain the absorption and emission spectra for tocopherols 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Absorption and emission wavelength  |2 nationallicence 
690 7 |a Solvent effect  |2 nationallicence 
690 7 |a TDDFT  |2 nationallicence 
690 7 |a Tocopherols  |2 nationallicence 
690 7 |a π→π* transition  |2 nationallicence 
700 1 |a Bakhouche  |D Kahina  |u Laboratoire de Thermodynamique et Modélisation Moléculaire (LTMM), Faculté de Chimie, USTHB BP 32, El Alia, 16111, Bab Ezzouar, Alger, Algeria  |4 aut 
700 1 |a Dhaouadi  |D Zoubeida  |u Laboratoire de Spectroscopie Atomique Moléculaire et Applications (LSAMA), Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, 1060, Tunis, Tunisia  |4 aut 
700 1 |a Lahmar  |D Souad  |u Laboratoire de Spectroscopie Atomique Moléculaire et Applications (LSAMA), Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, 1060, Tunis, Tunisia  |4 aut 
700 1 |a Hammoutène  |D Dalila  |u Laboratoire de Thermodynamique et Modélisation Moléculaire (LTMM), Faculté de Chimie, USTHB BP 32, El Alia, 16111, Bab Ezzouar, Alger, Algeria  |4 aut 
773 0 |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/6(2015-06-01), 1-13  |x 1610-2940  |q 21:6<1  |1 2015  |2 21  |o 894 
856 4 0 |u https://doi.org/10.1007/s00894-015-2706-1  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00894-015-2706-1  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Bakhouche  |D Kahina  |u Laboratoire de Thermodynamique et Modélisation Moléculaire (LTMM), Faculté de Chimie, USTHB BP 32, El Alia, 16111, Bab Ezzouar, Alger, Algeria  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Dhaouadi  |D Zoubeida  |u Laboratoire de Spectroscopie Atomique Moléculaire et Applications (LSAMA), Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, 1060, Tunis, Tunisia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lahmar  |D Souad  |u Laboratoire de Spectroscopie Atomique Moléculaire et Applications (LSAMA), Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, 1060, Tunis, Tunisia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hammoutène  |D Dalila  |u Laboratoire de Thermodynamique et Modélisation Moléculaire (LTMM), Faculté de Chimie, USTHB BP 32, El Alia, 16111, Bab Ezzouar, Alger, Algeria  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/6(2015-06-01), 1-13  |x 1610-2940  |q 21:6<1  |1 2015  |2 21  |o 894