11 research outputs found

    Hydrogen Abstraction from the C15 Position of the Cholesterol Skeleton

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    [EN] Cholesterol (Ch) is an integral part of cell membrane, where it is prone to oxidation. In humans, oxidation of Ch is commonly linked to various pathologies like Alzheimer's disease, atherosclerosis, and even cancer, which proceed via mechanisms involving enzymatic and free radical pathways. The latter begin with hydrogen abstraction (HA) from Ch by a reactive free radical. It has been established that the most efficient HA from Ch occurs at C7, although HA from C4 by peroxyl radicals has recently been observed. Conversely, HA from Ch positions other than the thermodynamically preferred C7 or C4 has never been reported. We have designed a Ch derivative where a benzophenone moiety is linked to C7 by a covalent bond. This mirrors a specific orientation of Ch within a confined environment. Product analysis and time-resolved spectroscopic studies reveal an unprecedented HA from C15, which is a thermodynamically unfavorable position. This indicates that a specific topology of reactants is crucial for the reactivity of Ch. The relative orientation of the reactants can also be relevant in biological membranes, where Ch, polyunsaturated fatty acids, and numerous oxidizing species are confined in highly restricted and anisotropic environments.This work was supported by the Carlos III Institute of Health (Grants No. PII6/01877, "Miguel Servet fellowship" CPII16/00052 to I.A.), and by the Generalitat Valenciana (Prometeo 2017/075). We would like to thank Dr Fedora Grande for sending an exchange student (M.B.). D.N. and G.G. thank NAWI Graz for support.Palumbo, F.; Andreu Ros, MI.; Brunetti, M.; Schmallegger, M.; Gescheidt, G.; Neshchadin, D.; Miranda Alonso, MÁ. (2019). Hydrogen Abstraction from the C15 Position of the Cholesterol Skeleton. The Journal of Organic Chemistry. 84(23):15184-15191. https://doi.org/10.1021/acs.joc.9b02181S15184151918423Zerbinati, C., & Iuliano, L. (2017). Cholesterol and related sterols autoxidation. Free Radical Biology and Medicine, 111, 151-155. doi:10.1016/j.freeradbiomed.2017.04.013Schroepfer, G. J. (2000). Oxysterols: Modulators of Cholesterol Metabolism and Other Processes. Physiological Reviews, 80(1), 361-554. doi:10.1152/physrev.2000.80.1.361Girotti, A. W., & Korytowski, W. (2017). Cholesterol Hydroperoxide Generation, Translocation, and Reductive Turnover in Biological Systems. Cell Biochemistry and Biophysics, 75(3-4), 413-419. doi:10.1007/s12013-017-0799-0Poli, G., Biasi, F., & Leonarduzzi, G. (2013). Oxysterols in the pathogenesis of major chronic diseases. Redox Biology, 1(1), 125-130. doi:10.1016/j.redox.2012.12.001Buttari, B., Segoni, L., Profumo, E., D’Arcangelo, D., Rossi, S., Facchiano, F., 
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    Proton-Coupled Electron Transfer from Hydrogen-Bonded Phenols to Benzophenone Triplets

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    Phenols with intramolecular hydrogen bond between a pendant base and the phenolic OH group react differently in polar and non-polar environments with electron/proton acceptors. This was demonstrated by using time resolved chemically induced dynamic nuclear polarization (TR CIDNP) and theoretical calculations. In benzene, those phenols undergo a concerted electron–proton transfer (EPT) that yields neutral ketyl and phenoxyl radicals. In polar acetonitrile, the reaction mechanism turns into an electron transfer from the phenol to the triplet ketone, accompanied by the shift of a proton from the phenolic OH group to the nitrogen atom of the pendant base to form a distonic radical cation. This behavior is similar to that of tyrosine H-bonded to basic residues in some radical enzymes. This solvent-induced mechanism switch in proton-coupled electron transfers is important in different biological systems, in which the same metabolites and intermediates can react differently depending on the specific local environments

    Transition Metal Azahemiporphycenes as Singlet Oxygen Sensitizers

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    Using free-base tris(p-X-phenyl)corrole (X = H, Me, OMe) as starting materials and 4-aminotriazole as the nitrogen source, we used a DDQ-mediated, room-temperature strategy for generating isocorrole synthesis to obtain the corresponding 6-azahemiporphycenes, H2[X-AHP], one of which was structurally characterized with single-crystal X-ray diffraction analysis. The free-base ligands were readily derivatized to their Pd(II), Pt(II), and Mn(II) complexes; of these, one Pd(II) complex was structurally characterized. Three of the complexes, M[Me-AHP] (M = Pd, Pt, Mn), were singled out for photophysical and singlet oxygen sensitization studies. Although none of the new complexes proved luminescent, Pd[Me-AHP] was found to be an excellent singlet oxygen sensitizer, with a singlet oxygen quantum yield of 84% in 9:1 v/v ethanol:tetrahydrofuran at room temperature. The corresponding value for Pt[Me-AHP] was found to be only 11% and that for Mn[Me-AHP] essentially 0%. These singlet oxygen quantum yields were consonant with triplet lifetimes accessed via transition absorption spectroscopy. Combined with their strong absorption in the red, these findings suggest that palladium 6-azahemiporphycenes are worthy of exploration as a new class of triplet photosensitizers for photodynamic therapy of cancer and other diseases

    Unprecedented bifunctional chemistry of bis(acyl)phosphane oxides in aqueous and alcoholic media

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    Tailor-made photoinitiators play an important role for efficient radical polymerisations in aqueous media, especially in hydrogel manufacturing. Bis(acyl)phosphane oxides (BAPOs) are among the most active initiators. Herein, we show that they display a remarkable photochemistry in aqueous and alcoholic media: Photolysis of BAPOs in the presence of water or alcohols provides a new delocalized π-radical, which does not participate in the polymerization. It either converts into a monoacylphosphane oxide acting as a secondary photoactive species or it works as a one-electron reducing agent. Upon the electron-transfer process, it again produces a dormant photoinitiator. We have established the structure and the chemistry of this π radical using steady-state and time-resolved (CIDEP) EPR together with ESI-MS, NMR spectroscopy, and DFT calculations. Our results show that bis(acyl)phosphane oxides act as bifunctional reagents when applied in aqueous and alcoholic media

    CCDC 1991959: Experimental Crystal Structure Determination

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    PADREV : 4,4'-dimethoxy[1,1'-biphenyl]-2,2',5,5'-tetrol Space Group: C 2 (5), Cell: a 24.488(16)Å b 5.981(4)Å c 3.911(3)Å, α 90° ÎČ 91.47(3)° Îł 90

    2‐Methoxyhydroquinone from Vanillin for Aqueous Redox‐Flow Batteries

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    We show the synthesis of a redox‐active quinone, 2‐methoxy‐1,4‐hydroquinone (MHQ), from a bio‐based feedstock and its suitability as electrolyte in aqueous redox flow batteries. We identified semiquinone intermediates at insufficiently low pH and quinoid radicals as responsible for decomposition of MHQ under electrochemical conditions. Both can be avoided and/or stabilized, respectively, using H 3 PO 4 electrolyte, allowing for reversible cycling in a redox flow battery for hundreds of cycles
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