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Furanyl chalcone derivatives as efficient singlet oxygen quenchers. An experimental and DFT/MRCI study

dc.contributor.authorDiaz-Uribe C.
dc.contributor.authorVallejo W.
dc.contributor.authorFlórez J.
dc.contributor.authorTrilleras J.
dc.contributor.authorGutierrez M.
dc.contributor.authorRodriguez-Serrano A.
dc.contributor.authorSchott E.
dc.contributor.authorZarate X.
dc.date.accessioned2020-09-02T22:16:51Z
dc.date.available2020-09-02T22:16:51Z
dc.date.issued2020
dc.identifier10.1016/j.tet.2020.131248
dc.identifier.citation76, 24, -
dc.identifier.issn00404020
dc.identifier.urihttps://hdl.handle.net/20.500.12728/4359
dc.descriptionThis study reports the antioxidant activity against singlet oxygen (1O2) of five newly synthesized furanyl chalcones (FCs) (E)-3-(5-(4-chlorophenyl)furan-2-yl)-1-arylprop-2-en-1-ones (3a-e). Their structural difference is based on the aryl substituent as follows (Ar): 3a = –C6H4–OCH3, 3b = –C6H3-(1,2-OCH3), 3c = –C6H4OC6H4, 3d = –C10H6-(OCH3) and 3e = –C4H3O. We used a Claisen-Schmidt condensation involving a 5-(4-chlorophenyl)furan-2-carbaldehyde and the corresponding ketones under ultrasonic irradiation. Their property to 1O2 quenching was analyzed in terms of the rate constant for the process (kQ at 25 °C) determined by the Stern–Volmer model in ethanol. For the compounds 3c, 3d and 3e, the kQ values are slightly larger respect to 3a and 3b. The FCs 3c behaves as the best quencher (kQ of 8.44 (±0.09) x 107 M−1s−1). Geometry analysis and electronic structure calculations have been performed in the framework of Density Functional Theory (DFT) and DFT/Multi-Reference Configuration Interaction (DFT/MRCI) methods. According to DFT/MRCI, a physical quenching of 1O2 from the ground states of the FCs may not likely induce a spontaneous energy transfer processes but a chemical quenching mechanism may dominate the kinetics. © 2020 Elsevier Ltd
dc.language.isoen
dc.publisherElsevier Ltd
dc.subjectDFT/MRCI
dc.subjectFuranyl chalcones
dc.subjectSinglet oxygen quenching
dc.subject3 [5 (4 chlorophenyl)furan 2 yl] 1 (3,4 dimethoxyphenyl)prop 2 en 1 one
dc.subject3 [5 (4 chlorophenyl)furan 2 yl] 1 (4 methoxyphenyl)prop 2 en 1 one
dc.subject3 [5 (4 chlorophenyl)furan 2 yl] 1 (4 phenoxyphenyl)prop 2 en 1 one
dc.subject3 [5 (4 chlorophenyl)furan 2 yl] 1 (6 methoxynaphthalen 2 yl)prop 2 en 1 one
dc.subject3 [5 (4 chlorophenyl)furan 2 yl] 1 (furan 2 yl)prop 2 en 1 one
dc.subjectchalcone derivative
dc.subjectsinglet oxygen
dc.subjectunclassified drug
dc.subjectanalytic method
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectClaisen rearrangement
dc.subjectdensity functional theory
dc.subjectdrug structure
dc.subjectdrug synthesis
dc.subjectenergy transfer
dc.subjectFourier transform infrared spectroscopy
dc.subjectkinetics
dc.subjectmultireference configuration interaction
dc.subjectpriority journal
dc.subjectproton nuclear magnetic resonance
dc.subjectrate constant
dc.subjectultrasound
dc.titleFuranyl chalcone derivatives as efficient singlet oxygen quenchers. An experimental and DFT/MRCI study
dc.typeArticle


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