6,079 research outputs found

    Cafeato de metilo butilado: un nuevo antioxidante

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    A novel caffeic acid derivative, butylated methyl caffeate (BMC), was synthesized via esterification between butylated caffeic acid (BCA) and methanol. Its antioxidant activity was investigated and compared to TBHQ, caffeic acid (CA), methyl caffeate (MC) and BCA through deep-frying, an oven test in oil-in-water emulsions and DPPH radical scavenging. BMC showed the strongest antioxidant activity among the five anti­oxidants in emulsions and its antioxidant activity was almost as strong as BCA in frying. Its soybean oil-water partition coefficient was 9.18 due to its ester and tert-butyl groups, far greater than those of MC (4.82), BCA (2.41), CA (0.84) and TBHQ (3.22). This meant that it was much more soluble in the lipid phase than the other four antioxidants in emulsions. The DPPH radical scavenging activity of BMC was near TBHQ, lower than the other three because of its steric hindrance and less functional phenolic hydroxyl groups compared to others when their masses were the same.Un novedoso derivado del ácido cafeico, el cafeato de metilo butilado (BMC), fue sintetizado mediante esterificación entre el ácido cafeico butilado (BCA) y el metanol. Se investigó su actividad antioxidante y se comparó con TBHQ, ácido cafeico (CA), cafeato de metilo (MC) y BCA mediante pruebas de fritura, pruebas en horno, en emulsiones de aceite en agua y mediante eliminación de radicales DPPH. BMC mostró la mayor actividad antioxidante entre los cinco antioxidantes en emulsiones y tenía una actividad antioxidante casi tan fuerte como la del BCA en fritura. Su coeficiente de partición aceite de soja-agua es de 9.18 debido a sus grupos éster y terc-butilo, mucho mayores que los de MC (4.82), BCA (2.41), CA (0.84) y TBHQ (3.22). Esto significa que es mucho más soluble en la fase lipídica que los otros cuatro antioxidantes cuando está en emulsiones. La actividad de captación de radicales DPPH de BMC fue cercana a la del TBHQ, más baja que las otras tres debido a su impedimento estérico y grupos hidroxilo fenólicos, menos funcionales en comparación con los otros cuando sus masas son iguales

    Un nuevo antioxidante: 6,6'-(butano-1,1-diil)bis(4-metil-benceno-1,2-diol)

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    A novel compound, 6,6'-(butane-1,1-diyl)bis(4-methylbenzene-1,2-diol) (BMB), was synthesized through an acid-catalyzed condensation reaction between 4-methylcatechol (HPC) and butyraldehyde. When evaluated by the Rancimat and deep frying methods, BMB exhibited a stronger antioxidant activity than TBHQ. Its DPPH radical scavenging activity was also fairly higher than TBHQ, but lower compared to its mother phenol, HPC, due to its relative ease of binding DPPH•. BMB had the strongest scavenging ability of the 4-methylcatechol analogues reported to date. It could be used effectively to retard lipid peroxidation in both moderate and high temperature food preparations.Un nuevo compuesto, 6,6'-(butano-1,1-diil)bis(4-metilbenceno-1,2-diol) (BMB) fue sintetizado mediante una reacción de condensación catalizada por ácido entre el 4-metilcatecol (HPC) y el butiraldehído. Cuando se evaluó mediante los métodos Rancimat y de fritura, el BMB mostró una actividad antioxidante más fuerte que el TBHQ. Su actividad de eliminación de radicales DPPH también fue bastante mayor que la del TBHQ, pero menor en comparación con el fenol de partida, HPC, debido a su relativa facilidad para unirse a DPPH•. BMB tiene una actividad de eliminación más fuerte que los análogos de 4-metilcatecol reportados hasta la fecha. Podría usarse eficazmente para retardar la peroxidación de lípidos en la preparación de alimentos a temperatura moderada y alta

    Mean-Field Description of Phase String Effect in the tJt-J Model

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    A mean-field treatment of the phase string effect in the tJt-J model is presented. Such a theory is able to unite the antiferromagnetic (AF) phase at half-filling and metallic phase at finite doping within a single theoretical framework. We find that the low-temperature occurrence of the AF long range ordering (AFLRO) at half-filling and superconducting condensation in metallic phase are all due to Bose condensations of spinons and holons, respectively, on the top of a spin background described by bosonic resonating-valence-bond (RVB) pairing. The fact that both spinon and holon here are bosonic objects, as the result of the phase string effect, represents a crucial difference from the conventional slave-boson and slave-fermion approaches. This theory also allows an underdoped metallic regime where the Bose condensation of spinons can still exist. Even though the AFLRO is gone here, such a regime corresponds to a microscopic charge inhomogeneity with short-ranged spin ordering. We discuss some characteristic experimental consequences for those different metallic regimes. A perspective on broader issues based on the phase string theory is also discussed.Comment: 18 pages, five figure

    Observation of momentum-confined in-gap impurity state in Ba0.6_{0.6}K0.4_{0.4}Fe2_2As2_2: evidence for anti-phase s±s_{\pm} pairing

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    We report the observation by angle-resolved photoemission spectroscopy of an impurity state located inside the superconducting gap of Ba0.6_{0.6}K0.4_{0.4}Fe2_2As2_2 and vanishing above the superconducting critical temperature, for which the spectral weight is confined in momentum space near the Fermi wave vector positions. We demonstrate, supported by theoretical simulations, that this in-gap state originates from weak non-magnetic scattering between bands with opposite sign of the superconducting gap phase. This weak scattering, likely due to off-plane Ba/K disorders, occurs mostly among neighboring Fermi surfaces, suggesting that the superconducting gap phase changes sign within holelike (and electronlike) bands. Our results impose severe restrictions on the models promoted to explain high-temperature superconductivity in these materials.Comment: 8 pages, 5 figures. Accepted for publication in Physical Review

    Relación estructura-actividad antioxidante de compuestos fenólicos impedidos estéricamente

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    The relationship between the structure and the antioxidant activity of 21 hindered phenolic compounds was investigated by Rancimat and DPPH· tests. 3-tert-butyl-5-methylbenzene-1,2-diol is the strongest antioxidant in the Rancimat test but not in the DPPH· test because its two hydroxyl groups have very strong steric synergy. 2,6-Ditert-butyl-4-hydroxy-methylphenol exhibits a strong antioxidant activity as 2,6-ditertbutyl- 4-methoxyphenol does in lard. 2,6-Ditert-butyl-4- hydroxy-methylphenol also exhibits stronger activity than 2-tert-butyl-4- methoxyphenol. The methylene of 2,6-ditert-butyl-4-hydroxy-methylphenol can provide a hydrogen atom to active free radicals like a phenolic hydroxyl group does because it is greatly activated by both the aromatic ring and hydroxyl group. Five factors affect the antioxidant activities of the phenolic compounds: how stable the phenolic compound free radicals are after providing hydrogen atoms; how many hy drogen atoms each of the phenolic compounds can provide; how fast the phenolic compounds provide hydrogen atoms; how easily the phenolic compound free radicals can combine with more active free radicals, and whether or not a new antioxidant can form after the phenolic compound provides hydrogen atoms.La relación entre estructura y la actividad antioxidante de 21 compuestos fenólicos con impedimentos estéricos fue investigado mediante ensayos con Rancimat y DPPH·. El 3-terc-butil-5-metilbenceno-1,2-diol es el antioxidante más potente en los ensayos mediante Rancimat pero no mediante ensayos con DPPH·, porque sus dos grupos hidroxilo tienen una fuerte sinergia estérica. El 2,6-Di-terc-butil-4-hidroxi-metil-fenol mostró una actividad antioxidante tan fuerte como el 2,6-di-ter-butil-4-metoxifenol en ensayos con manteca de cerdo. El 2,6-di-terc-butil-4-hidroxi-metilfenol también mostró una actividad más fuerte que el 2-terc-butil-4-metoxifenol. El grupo metileno del 2,6-di-ter-butil-4-hidroxi-metilfenol puede suministrar átomos de hidrógeno y activar radicales libres como lo hace un grupo hidroxilo fenólico porque se activa en gran medida tanto por anillo aromático como por el grupo hidroxilo. Cinco factores afectan a la actividad antioxidante de los compuestos fenólicos: cómo de estable son los radicales libres de los compuestos fenólicos después de suministrar átomos de hidrógeno; cuántos átomos de hidrógeno pueden proporcionar cada uno de los compuestos fenólicos; la rapidez con la que los compuestos fenólicos donen átomos de hidrógeno; la facilidad con la que los radicales libres de los compuestos fenólicos pueden combinarse con los radicales libres más activos, y si es o no un nuevo antioxidante el que se puede formar después de que el compuesto fenólico done los átomos de hidrógeno

    Observation of Weyl nodes in TaAs

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    In 1929, H. Weyl proposed that the massless solution of Dirac equation represents a pair of new type particles, the so-called Weyl fermions [1]. However the existence of them in particle physics remains elusive for more than eight decades. Recently, significant advances in both topological insulators and topological semimetals have provided an alternative way to realize Weyl fermions in condensed matter as an emergent phenomenon: when two non-degenerate bands in the three-dimensional momentum space cross in the vicinity of Fermi energy (called as Weyl nodes), the low energy excitation behaves exactly the same as Weyl fermions. Here, by performing soft x-ray angle-resolved photoemission spectroscopy measurements which mainly probe bulk band structure, we directly observe the long-sought-after Weyl nodes for the first time in TaAs, whose projected locations on the (001) surface match well to the Fermi arcs, providing undisputable experimental evidence of existence of Weyl fermion quasiparticles in TaAs.Comment: 10 pages, 4 figures, see also related papers on TaAs arXiv:1501.00060, arXiv:1502.0468

    Effect of allicin on THP-1, MT-2 and WISH cell apoptosis induced by vesicular stomatitis virus (VSV) and the molecular mechanism involved

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    Vesicular stomatitis virus (VSV) has been reported to induce apoptosis and the onset of apoptosis may play an important role in virus-associated diseases. This study was conducted in order to investigate the protective effect of the herbal constituent allicin on VSV-induced apoptosis in the human monocyte line THP-1, human T lymphocytic leukemia cell line MT-2 and human amniotic cell line WISH and to determine the possible molecular mechanism involved. The THP-1, MT-2 and WISH cells were incubated with VSV in the absence or presence of different doses of allicin (10, 25 and 50 μg/ml). To study apoptosis, the cells were assessed by MTT and annexin V-propidium iodide double-staining flow cytometry. To investigate the molecular mechanism by which allicin regulates VSV-induced THP-1, MT-2 and WISH cell apoptosis, the expression of active cleavage products of caspases 3, 6, 7 and 9 and NF-κB was analyzed by western blotting. Our results indicated that allicin did not affect the adhesion and entry of VSV into THP-1, MT-2 or WISH cells. Using different concentrations of allicin, a dose-dependent protective effect on  cell apoptosis was observed. In addition, the VSV-induced expression of active cleavage products of caspases 3, 6, 7 and 9 and NF-κB in THP-1, MT-2 and WISH cells was also significantly reduced by allicin at the protein level. We concluded that allicin protects THP-1, MT-2 and WISH cells from VSV-induced apoptosis by inhibiting the activation of caspases 3, 6, 7 and 9 and NF-κB, thereby suggesting a potential protective effect for allicin against virus-associated diseases.Key words: Allicin, vesicular stomatitis virus (VSV), apoptosis, caspases, NF-κB

    Deep Learning Enabled Semantic Communications with Speech Recognition and Synthesis

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    In this paper, we develop a deep learning based semantic communication system for speech transmission, named DeepSC-ST. We take the speech recognition and speech synthesis as the transmission tasks of the communication system, respectively. First, the speech recognition-related semantic features are extracted for transmission by a joint semantic-channel encoder and the text is recovered at the receiver based on the received semantic features, which significantly reduces the required amount of data transmission without performance degradation. Then, we perform speech synthesis at the receiver, which dedicates to re-generate the speech signals by feeding the recognized text and the speaker information into a neural network module. To enable the DeepSC-ST adaptive to dynamic channel environments, we identify a robust model to cope with different channel conditions. According to the simulation results, the proposed DeepSC-ST significantly outperforms conventional communication systems and existing DL-enabled communication systems, especially in the low signal-to-noise ratio (SNR) regime. A software demonstration is further developed as a proof-of-concept of the DeepSC-ST
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