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31.
New coumarin derivatives, namely 7-[(5-amino-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one, 5-[(2-oxo-2H-chromen-7-yloxy)methyl]-1,3,4-thiadiazol-2(3H)-one, 2-[2-(2-oxo-2H-chromen-7-yloxy)acetyl]-N-phenylhydrazinecarbothioamide, 7-[(5-(phenylamino)-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one and 7-[(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)methoxy]-2H-chromen-2-one were prepared starting from the natural compound umbelliferone. The newly synthesized compounds were characterized by elemental analysis and spectral studies (IR, 1H-NMR and 13C-NMR). 相似文献
32.
Sabri S. Mahmoud Mohammed A. Hassan Fayez H. El-Khatib Ayman A. Obaidat Mutaz Sheikh-Salem 《Reaction Kinetics and Catalysis Letters》2000,70(1):119-124
Photodegradation of tenoxicam was investigated under different reaction conditions. After 60 min of exposure to UV light, the photodegradation was extensive, and the maximum and minimum in the UV-visible spectrum were shifted to shorter and longer wavelengths, respectively. Ethanol exerted a photostabilizing effect on tenoxicam. Tenoxicam is more stable in acidic and basic media than in neutral solution. Increasing light intensity or temperature causes an increase in the rate of photodegradation. The photodegradation of tenoxicam was found to follow first-order kinetics under all these conditions. 相似文献
33.
Mohamad Rafi Lee Wah Lim Toyohide Takeuchi Latifah Kosim Darusman 《Analytical and bioanalytical chemistry》2013,405(20):6599-6603
Fingerprint analysis using capillary liquid chromatography (CLC) has been developed for discrimination of Zingiber montanum (ZM) from related species, for example Z. americans (ZA) and Z. zerumbet (ZZ). By comparing the fingerprint chromatograms of ZM, ZA, and ZZ we could identify ZM samples and discriminate them from ZA and ZZ by using their marker peaks. We also combined CLC fingerprint with multivariate analysis, including principal-component analysis (PCA) and canonical variate analysis (CVA); all three species were discriminated successfully. This result indicates that CLC fingerprint analysis in combination with PCA and CVA can be used for discrimination of ZM samples from samples of related species. Figure
? 相似文献
34.
Bhan A Allian AD Sunley GJ Law DJ Iglesia E 《Journal of the American Chemical Society》2007,129(16):4919-4924
The acid-catalyzed formation of carbon-carbon bonds from C1 precursors via CO insertion into chemisorbed methyl groups occurs selectively within eight-membered ring (8-MR) zeolite channels. This elementary step controls catalytic carbonylation rates of dimethyl ether (DME) to methyl acetate. The number of O-H groups within 8-MR channels was measured by rigorous deconvolution of the infrared bands for O-H groups in cation-exchanged and acid forms of mordenite (M,H-MOR) and ferrierite (H-FER) after adsorption of basic probe molecules of varying size. DME carbonylation rates are proportional to the number of O-H groups within 8-MR channels. Na+ cations selectively replaced protons within 8-MR channels and led to a disproportionate decrease in carbonylation turnover rates (per total H+). These conclusions are consistent with the low or undetectable rates of carbonylation on zeolites without 8-MR channels (H-BEA, H-FAU, H-MFI). Such specificity of methyl reactivity upon confinement within small channels appears to be unprecedented in catalysis by microporous solids, which typically select reactions by size exclusion of bulkier transition states. 相似文献
35.
The present research work describes the productive synthesis of novel bisbenzopyronopyran derivatives 4(a-h) and 5(a-h) via the photocyclization reactions of bischromones 3(a-h) under the inert conditions. The latter compounds have been realized efficiently through the O-alkylation reactions of the 3-hydroxychromone 2 with suitable dihalogenated aliphatic/aromatic/heteroaromatic reagents in the presence of dry acetone/anhydrous K2CO3/Bu4N+I− (PTC). The cyclization reaction of chalcone 1 under the Algar-Flynn-Oyamada reaction conditions (KOH/H2O2) could results in the formation of compound 2 in the good yield. The structural scaffolds of the newly prepared bischromones and resultant bisbenzopyronopyrans have been certified from the meticulous analysis of their various spectroscopic parameters such as UV-Vis, IR, 1H/13C-NMR, and ESI-MS. It was found that o/m/p-xylene and pyridine-linked final symmetrical bistetracycles exhibited higher antimicrobial potencies as compared to alkyl chain-linked cyclized products. The bischromones 3(a-h) could be able to endow modest level of antimicrobial behavior. 相似文献
36.
Samsul Rizal N. I. Saharudin N. G. Olaiya H. P. S. Abdul Khalil M. K. Mohamad Haafiz Ikramullah Ikramullah Umar Muksin Funmilayo G. Olaiya C. K. Abdullah Esam Bashir Yahya 《Molecules (Basel, Switzerland)》2021,26(7)
The degradation and mechanical properties of potential polymeric materials used for green manufacturing are significant determinants. In this study, cellulose nanofibre was prepared from Schizostachyum brachycladum bamboo and used as reinforcement in the PLA/chitosan matrix using melt extrusion and compression moulding method. The cellulose nanofibre(CNF) was isolated using supercritical carbon dioxide and high-pressure homogenisation. The isolated CNF was characterised with transmission electron microscopy (TEM), FT-IR, zeta potential and particle size analysis. The mechanical, physical, and degradation properties of the resulting biocomposite were studied with moisture content, density, thickness swelling, tensile, flexural, scanning electron microscopy, thermogravimetry, and biodegradability analysis. The TEM, FT-IR, and particle size results showed successful isolation of cellulose nanofibre using this method. The result showed that the physical, mechanical, and degradation properties of PLA/chitosan/CNF biocomposite were significantly enhanced with cellulose nanofibre. The density, thickness swelling, and moisture content increased with the addition of CNF. Also, tensile strength and modulus; flexural strength and modulus increased; while the elongation reduced. The carbon residue from the thermal degradation and the glass transition temperature of the PLA/chitosan/CNF biocomposite was observed to increase with the addition of CNF. The result showed that the biocomposite has potential for green and sustainable industrial application. 相似文献
37.
Ayman H. Kamel Nashwa H. Ashmawy Teraze A. Youssef Mostafa Elnakib Heba Abd El-Naby Hisham S. M. Abd-Rabboh 《Electroanalysis》2023,35(7):e202200436
Herein, two electrochemical methods based on potentiometric and impedimetric transductions were presented for albumin targeting, employing screen-printed platforms (SPEs) to make easy and cost-effective sensors with good detection merits. The SPEs incorporated ion-to-electron multi-walled carbon nanotubes (MWCNTs) transducer. Sensors were constructed using either tridodecyl methyl-ammonium chloride (TDMACl) (sensor I) or aliquate 336S (sensor II) in plasticized polymeric matrices of carboxylated poly (vinyl chloride) (PVC-COOH). Analytical performances of the sensors were evaluated using the above-mentioned electrochemical techniques. For potentiometric assay, constructed sensors responded to albumin with −81.7 ± 1.7 (r2 = 0.9986) and −146.2 ± 2.3 mV/decade (r2 = 0.9991) slopes over the linearity range 1.5 μM–1.5 mM with 0.8 and 1.0 μM detection limits for respective TDMAC- and aliquate-based sensors. Interference study showed apparent selectivity for both sensors. Impedimetric assays were performed at pH = 7.5 in 10 mM PBS buffer solution with a 0.02 M [Fe(CN)6]−3/−4 redox-active electrolyte. Sensors achieved detection limits of 4.3 × 10−8 and 1.8 × 10−7 M over the linear ranges of 5.2×10−8–1.0×10−4 M and 1.4×10−6–1.4×10−3 M, with 0.09 ± 0.004 and 0.168 ± 0.009 log Ω/decade slopes for sensors based on TDMAC and aliquate, respectively. These sensors are characterized with simple construction, high sensitivity and selectivity, fast response time, single-use, and cost-effectiveness. The methods were successfully applied to albumin assessment in different biological fluids. 相似文献
38.
39.
On the Synthesis,Characterization and Reactivity of N‐Heteroaryl–Boryl Radicals,a New Radical Class Based on Five‐Membered Ring Ligands 下载免费PDF全文
Dr. Mohamad‐Ali Tehfe Dr. Stéphane Schweizer Dr. Anne‐Caroline Chany Dr. Cédric Ysacco Dr. Jean‐Louis Clément Dr. Didier Gigmes Dr. Fabrice Morlet‐Savary Prof. Jean‐Pierre Fouassier Dr. Markus Neuburger Dr. Théophile Tschamber Dr. Nicolas Blanchard Prof. Jacques Lalevée 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(17):5054-5063
The synthesis and physical characterization of a new class of N‐heterocycle–boryl radicals is presented, based on five membered ring ligands with a N(sp2) complexation site. These pyrazole–boranes and pyrazaboles exhibit a low bond dissociation energy (BDE; B?H) and accordingly excellent hydrogen transfer properties. Most importantly, a high modulation of the BDE(B?H) by the fine tuning of the N‐heterocyclic ligand was obtained in this series and could be correlated with the spin density on the boron atom of the corresponding radical. The reactivity of the latter for small molecule chemistry has been studied through the determination of several reaction rate constants corresponding to addition to alkenes and alkynes, addition to O2, oxidation by iodonium salts and halogen abstraction from alkyl halides. Two selected applications of N‐heterocycle–boryl radicals are also proposed herein, for radical polymerization and for radical dehalogenation reactions. 相似文献
40.
Ayman Nafady Ylias Mohammad Sabri Ahmad Esmaielzadeh Kandjani Ali M. Alsalme Alan M. Bond Suresh Bhargava 《Journal of Solid State Electrochemistry》2016,20(12):3303-3314
Facile synthesis and characterization of the highly conducting, thermodynamically favored, Tl(TCNQ) phase II microrods/nanorods onto conducting (glassy carbon (GC)) and semiconducting (indium tin oxide (ITO)) surfaces have been accomplished via redox-based transformation of 7,7,8,8-tetracynoquinodimethane (TCNQ) microcrystals. This electrochemically irreversible process involves the one-electron reduction of surface-confined solid TCNQ into TCNQ·? with concomitant incorporation of the Tl+ (aq) cation, from the bulk solution, at the triple-phase boundary, GC or ITO│(TCNQ(s)/TCNQ·? (s))│Tl+ (aq), through a nucleation/growth mechanism. Consistent with the conceptually related M(TCNQ) systems (M+ = Li+, Na+, K+, Ag+, and Cu+), the TCNQ/Tl(TCNQ) interconversion is strongly dependent upon scan rate, Tl+ (aq) electrolyte concentration, and the method of attaching solid TCNQ onto the electrode surface. Spectroscopic (infrared (IR) and Raman), microscopic (scanning electron microscopy (SEM)), and surface science (X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray (EDX), and X-ray diffraction (XRD)) characterization of the electrochemically synthesized material revealed formation of pure Tl(TCNQ) phase II. Importantly, the generic solid-state electrochemical approach used in this study not only offers facile protocol for controllable and preferential synthesis of Tl(TCNQ) phase II but also provides access to fabricate and tune the morphology to yield microrod/nanorod networks. 相似文献