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991.
Oana-Viorela Nistor Carmen Alina Bolea Doina-Georgeta Andronoiu Mihaela Cotrle Nicoleta Stnciuc 《Molecules (Basel, Switzerland)》2021,26(11)
Sea buckthorn (Hippophaė rhamnoides L.) is recognized as a valuable source of vitamin C and antioxidants, frequently used as nutraceuticals and cosmeceuticals. In the present study, attempts are made to produce and characterize a novel type of marmalade using sea buckthorn berries processed at 102 °C into marmalade in two combinations, with whole cane or stevia sugar. Changes in the phytochemical profile, antioxidant activity, color, shelf-life, texture, microbiological, and sensorial characteristics were determined. The total carotenoids content in the marmalades were significantly different, with values of 0.91 ± 0.03 mg/g dry weight (DW) in the sample with whole sugar cane (Cz) and 2.69 ± 0.14 mg/g DW in the sample with Stevia sugar (Cs). Significant values of polyphenols were found, of 59.41 ± 1.13 mg GAE/g DW in Cz and 72.44 ± 2.31 mg GAE/g DW in Cs, leading to an antioxidant activity of 45.12 ± 0.001 μMol Trolox/g DW and 118.07 ± 0.01 μMol Trolox/g DW, respectively. Accelerated storage study showed a decrease in all the phytochemicals, however no significant changes were found in antioxidant activity. Values of <100 CFU/g for yeasts and molds and <5 CFU/g for Enterobacteriaceae after 21 days of storage at the room temperature of the marmalades were determined. The sensorial and color results were more than acceptable. Overall, the results highlighted the potential of using sea buckthorn as a potential rich source of bioactive compounds to be used in the sugar-based products manufacturing. 相似文献
992.
Xiao-Qian Xu Dr. Li-Hui Cao Yan Yang Xiang-Tian Bai Fang Zhao Dr. Zhen-Hong He Dr. Zheng Yin Prof. Dr. Yang-Min Ma 《化学:亚洲杂志》2021,16(2):142-146
Over the past two decades, progress in chemistry has generated various types of porous materials for removing iodine (129I or 131I) that can be formed during nuclear energy generation or nuclear waste storage. However, most studies for iodine capture are based on the weak host-guest interactions of the porous materials. Here, we present two cationic nonporous macrocyclic organic compounds, namely, MOC-1 and MOC-2 , in which 6I- and 8I− were as counter anions, for highly efficient iodine capture. MOC-1 and MOC-2 were formed by reacting 1,1′-diamino-4,4′-bipyridylium di-iodide with 1,2-diformylbenzene or 1,3-diformylbenzene, respectively. The presence of a large number of I− anions results in high I2 affinity with uptake capacities up to 2.15 g ⋅ g−1 for MOC-1 and 2.25 g ⋅ g−1 for MOC-2 . 相似文献
993.
Synthesis and characterization of a family of layered trichalcogenides for assisted hydrogen photogeneration
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Three layered trisulfides (TiS3, ZrS3, HfS3) have been synthesized by solid–gas reaction between metal and sulfur in a vacuum sealed ampoule at 550 °C during 60 h. The samples used in this work were prepared from a colloidal suspension of powder of each one of the metal trisulfides (MS3, M = Ti, Zr, Hf) in ethanol and deposited on titanium disks and quartz substrates by ”drop coating” technique. These samples have been characterized by X‐ray diffraction, energy dispersive analysis of X‐ray and scanning electron microscopy. The obtained direct optical band gaps are 1.0 ± 0.1 eV, 2.0 ± 0.1 eV and 2.2 ± 0.1 eV for TiS3, ZrS3 and HfS3, respectively. Photoelectrochemical measurements in 0.5 M Na2SO3 have been carried out to characterize the MS3/electrolyte interface. The flat‐band potentials (Vfb) vs. Ag/AgCl measured by electrochemical impedance spectroscopy (EIS) are –0.84 ± 0.02 V (TiS3), –0.93 ± 0.02 V (ZrS3) and –0.92 ± 0.02 V (HfS3). Hydrogen generation was investigated in a photoelectrochemical cell (PEC) with MS3 as photoanodes under white light illumination of 200 ± 20 mW/cm2 at external bias potentials of 0.3 V vs. Ag/AgCl. Hydrogen evolution flows have been quantified by quadrupole mass spectrometry (QMS) reaching instantaneous values up to 19 ± 2 nmol H2/min cm2 with TiS3 as photoanode. 相似文献
994.
Laredo E Prutsky N Bello A Grimau M Castillo RV Müller AJ Dubois P 《The European physical journal. E, Soft matter》2007,23(3):295-303
Thermally stimulated depolarization currents, TSDC, wide-angle X-ray scattering, WAXS, differential scanning calorimetry,
DSC, and polarized light optical microscopy, PLOM, have been used to examine poly(L-lactide)-b -poly(
-caprolactone) diblock copolymers in a wide composition range. Both components are crystallizable and the miscibility in
the amorphous phase has been determined from the behavior of the primary relaxations which are the dielectric manifestation
of the glass transition, and also from the superstructural morphology revealed by PLOM and the compositional dependence of
the melting points as determined by DSC. Distinct segmental mobilities in the amorphous phase which can be well resolved by
TSDC are present; the
mode of the slower component shifts to lower temperatures as the PCL content increases while the glass transition of neat
PCL is present for all compositions. A relaxation times bimodal distribution is apparent for PCL-rich copolymers. The composition
dependence of the multiple glass transitions detected in these weakly segregated copolymers are predicted by the self-concentration
model for a miscible blend made of components with a large Tg contrast. 相似文献
995.
D. Vignolles A. Audouard V. N. Laukhin J. Béard E. Canadell N. G. Spitsina E. B. Yagubskii 《The European Physical Journal B - Condensed Matter and Complex Systems》2007,55(4):383-388
The oscillatory magnetoresistance spectrum of the
organic metal (BEDO)5Ni(CN)4. 3C2H4(OH)2 has
been studied up to 50 T, in the temperature range from 1.5 K to
4.2 K. In high magnetic field, its Fermi surface corresponds to a
linear chain of quasi-two-dimensional orbits coupled by magnetic
breakdown (MB). The scattering rate consistently deduced from the
data relevant to the basic α and the MB-induced β
orbits is very large which points to a significant reduction of
the chemical potential oscillation. Despite of this feature, the
oscillations spectrum exhibits many frequency combinations. Their
effective masses and (or) Dingle temperature are not in agreement
with either the predictions of the quantum interference model or
the semiclassical model of Falicov and Stachowiak. 相似文献
996.
Bumhee Lim Yangyang Cheng Takehiro Kato Anh-Tuan Pham Eliott Le Du Abhaya Kumar Mishra Elija Grinhagena Dimitri Moreau Naomi Sakai Jerome Waser Stefan Matile 《Helvetica chimica acta》2021,104(8):e2100085
Thiol-mediated uptake is emerging as method of choice to penetrate cells. This study focuses on irreversible covalent inhibitors of thiol-mediated uptake. High-content high-throughput screening of the so far largest collection of hypervalent iodine reagents affords inhibitors that are more than 250 times more active than Ellman’s reagent and rival the best dynamic covalent inhibitors. Comparison with other irreversible reagents reveals that inhibition within one series follows reactivity, whereas inhibition across series deviates from reactivity. These trends support that molecular recognition, besides dynamic covalent exchange, contributes significantly to thiol-mediated uptake. The most powerful inhibitors besides the best hypervalent iodine reagents were Fukuyama’s nosyl protecting group and super-cinnamaldehydes that have been introduced as irreversible activators of the pain receptor TRPA1. Considering that several viruses use different forms of thiol-mediated uptake to enter cells, the identification of new irreversible inhibitors of thiol-mediated uptake is of general interest for the discovery of new antivirals. 相似文献
997.
Gabriella Kervefors Kumar Bhaskar Pal Gergely L. Tolnai Mukul Mahanti Hakon Leffler Ulf J. Nilsson Berit Olofsson 《Helvetica chimica acta》2021,104(2):e2000220
β-Galactose derivatives have recently been reported to selectively inhibit galectin-3, and a library of O3-arylated galactosides with varying substitution patterns was designed to study such inhibitions further. The O3-arylated galactosides were synthesized using diaryliodonium salts under mild and transition metal free conditions, providing the target products in moderate to good yields. An O3-trifluoroethylated galactoside was also synthesized using iodonium salt chemistry. Azido-substituted products were subsequently transformed into the corresponding triazoles. After deprotection, a selection of galactoside derivatives were evaluated for inhibitory potencies against galectins-1, 3, 4 N (N-terminal domain), 4 C (C-terminal domain), 7, 8 N, 8 C, 9 N, and 9 C and one compound with promising affinity and selectivity for both the N- and C-terminal domain of galectin-9 was discovered. 相似文献
998.
Lucien Eisenburger Prof. Dr. Oliver Oeckler Prof. Dr. Wolfgang Schnick 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(13):4461-4465
Tetrahedra-based nitrides with network structures have emerged as versatile materials with a broad spectrum of properties and applications. Both nitridosilicates and nitridophosphates are well-known examples of such nitrides that upon doping with Eu2+ exhibit intriguing luminescence properties, which makes them attractive for applications. Nitridosilicates and nitridophosphates show manifold structural variability; however, no mixed nitridosilicatephosphates except SiPN3 and SiP2N4NH have been described so far. The compounds AESiP3N7 (AE=Sr, Ba) were synthesized by a high-pressure high-temperature approach using the multianvil technique (8 GPa, 1400–1700 °C) starting from the respective alkaline earth azides and the binary nitrides P3N5 and Si3N4. The latter were activated by NH4F, probably acting as a mineralizing agent. SrSiP3N7 and BaSiP3N7 were obtained as single crystals. They crystallized in the barylite-1O (M=Sr) and barylite-2O structure types (M=Ba), respectively, with P and Si being occupationally disordered. Cation disorder was further supported by solid-state NMR spectroscopy and energy-dispersive X-ray spectroscopy (EDX) mapping of BaSiP3N7 with atomic resolution. Upon doping with Eu2+, both compounds showed blue emission under UV excitation. 相似文献
999.
Dr. Christian M. Hoidn Dr. Daniel J. Scott Prof. Dr. Robert Wolf 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(6):1886-1902
Recently there has been great interest in the reactivity of transition-metal (TM) centers towards white phosphorus (P4). This has ultimately been motivated by a desire to find TM-mediated alternatives to the current industrial routes used to transform P4 into myriad useful P-containing products, which are typically indirect, wasteful, and highly hazardous. Such a TM-mediated process can be divided into two steps: activation of P4 to generate a polyphosphorus complex TM-Pn, and subsequent functionalization of this complex to release the desired phosphorus-containing product. The former step has by now become well established, allowing the isolation of many different TM-Pn products. In contrast, productive functionalization of these complexes has proven extremely challenging and has been achieved only in a relative handful of cases. In this review we provide a comprehensive summary of successful TM-Pn functionalization reactions, where TM-Pn must be accessible by reaction of a TM precursor with P4. We hope that this will provide a useful resource for continuing efforts that are working towards this highly challenging goal of modern synthetic chemistry. 相似文献
1000.
Dr. Lewis C. H. Maddock Rebekka Morton Dr. Alan R. Kennedy Prof. Dr. Eva Hevia 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(61):15181-15187
Alkali-metal ferrates containing amide groups have emerged as regioselective bases capable of promoting Fe−H exchanges of aromatic substrates. Advancing this area of heterobimetallic chemistry, a new series of sodium ferrates is introduced incorporating the bulky arylsilyl amido ligand N(SiMe3)(Dipp) (Dipp=2,6-iPr2-C6H3). Influenced by the large steric demands imposed by this amide, transamination of [NaFe(HMDS)3] (HMDS=N(SiMe3)2) with an excess of HN(SiMe3)(Dipp) led to the isolation of heteroleptic [Na(HMDS)2Fe{N(SiMe3)Dipp}]∞ ( 1 ) resulting from the exchange of just one HMDS group. An alternative co-complexation approach, combining the homometallic metal amides [NaN(SiMe3)Dipp] and [Fe{N(SiMe3)Dipp}2] induces lateral metallation of one Me arm from the SiMe3 group in the iron amide furnishing tetrameric [NaFe{N(SiCH2Me2)Dipp}{N(SiMe3)Dipp}]4 ( 2 ). Reactivity studies support that this deprotonation is driven by the steric incompatibility of the single metal amides rather than the basic capability of the sodium reagent. Displaying synergistic reactivity, heteroleptic sodium ferrate 1 can selectively promote ferration of pentafluorobenzene using one of its HMDS arms to give heterotrileptic [Na{N(SiMe3)Dipp}(HMDS)Fe(C6F5)]∞ ( 4 ). Attempts to deprotonate less activated pyridine led to the isolation of NaHMDS and heteroleptic Fe(II) amide [(py)Fe{N(SiMe3)Dipp}(HMDS)] ( 5 ), resulting from an alternative redistribution process which is favoured by the Lewis donor ability of this substrate. 相似文献