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排序方式: 共有244条查询结果,搜索用时 171 毫秒
1.
Research on Chemical Intermediates - A polymer-supported Brønsted acid-functionalized Zn–porphyrin complex, knotted with benzimidazolium moiety (PSBAZnPP), has been synthesized and... 相似文献
2.
We present here an efficient method for the hydroboration of aldimines (-C=N-) with pinacolborane (HBpin) using an alkali metal catalyst, potassium benzyl. The reaction was accomplished with unprecedented catalytic efficiency under mild and solvent-free conditions to afford the high yield of the corresponding N-boryl amines up to 97%. Various functionalities on aldimines were incorporated for hydroboration. The corresponding boryl amines were subjected to further hydrolysis to yield the corresponding secondary amines with good yields up to 89%. This protocol for the reaction demonstrates an atom-economic and green method with diverse imines that bears excellent functional group tolerance. Chemoselective reduction of imines was also attained, with good yields of 74–89%. We also propose the most plausible mechanism involving the formation of metal hydride as the active pre-catalyst. 相似文献
3.
Harshika Agarwal Shweta Yadav Gautam Jaiswar 《Journal of Thermal Analysis and Calorimetry》2017,129(3):1471-1479
The thermal, morphological and optical studies of BaSO4 and MMT (nanoclay) embedded in PVDF were investigated. Nanocomposites samples of PVDF–BaSO4–MMT were prepared by varying the loadings (1–4 mass%) in case of BaSO4 and MMT nanomaterials, respectively. Polyvinylidene fluoride–barium sulfate-montmorillonite (PVDF–BaSO4–MMT) nanocomposites were prepared by solvent-mixing technique. Nanoparticles were synthesized by in situ deposition technique with the help of nonionic polymeric surfactant, and the particle size of nanoparticles was recognized by scanning electron microscopy (SEM) analysis which confirms that the particle has diameter of 80–90 nm. As prepared, nanocomposites films (thickness, 25 μm) were characterized by Fourier transform infrared microscopy (FTIR), SEM and electron diffraction spectroscopy (EDS). FTIR shows that all the chemical constituents were present in the nanocomposites, whereas SEM analysis suggested that the nanofillers dispersed well in polymer matrix and EDS showed the elemental composition of nanocomposite samples. Thermal properties of nanocomposites were studied by using TG/DTA/DTG. TG/DTA studies showed decomposition temperature of pure PVDF is 473.5 °C. The decomposition temperature (T d) of nanocomposites was increased by 93 °C in case of nanocomposites with addition of both BaSO4 and MMT nanomaterials. The difference in the thermal degradation temperature was found to be 1.2% higher in case of addition of BaSO4 nanoparticle as compared to nanoclay. The obtained transparent nanocomposite films were characterized by using UV–Vis spectrophotometer which shows that transparencies of nanocomposites are maintained in visible region, the intensity of absorption band in UV region is increased with the addition of BaSO4 nanoparticles, while in case of addition of nanoclay the UV region does not show drastic changes. Addition of both nanoparticle and nanoclay shows higher absorption in comparison with the individual samples. But further, doubling the amount of nanoparticle and nanoclay shows decrease in UV absorption. Overall, the results of thermal studies show that the incorporation of BaSO4 and MMT could significantly improve the thermal properties of nanocomposites. 相似文献
4.
Somaiyeh Charoughchi Jiang Tian Liu Melissa Berteau-Rainville Hannes Hase Mohammad S. Askari Shubham Bhagat Pat Forgione Ingo Salzmann 《Angewandte Chemie (International ed. in English)》2023,62(31):e202304964
Molecular p-dopants designed to undergo electron transfer with organic semiconductors are typically planar molecules with high electron affinity. However, their planarity can promote the formation of ground-state charge transfer complexes with the semiconductor host and results in fractional instead of integer charge transfer, which is highly detrimental to doping efficiency. Here, we show this process can be readily overcome by targeted dopant design exploiting steric hindrance. To this end, we synthesize and characterize the remarkably stable p-dopant 2,2′,2′′-(cyclopropane-1,2,3-triylidene)tris(2-(perfluorophenyl)acetonitrile) comprising pendant functional groups that sterically shield its central core while retaining high electron affinity. Finally, we demonstrate it outperforms a planar dopant of identical electron affinity and increases the thin film conductivity by up to an order of magnitude. We believe exploiting steric hindrance represents a promising design strategy towards molecular dopants of enhanced doping efficiency. 相似文献
5.
Haritha Rajaram N. Harshitha Shweta A. Ram Swarna M. Patra Vidya Niranjan K.A. Vishnumurthy 《印度化学会志》2022,99(6):100488
In the present study, the main protease 3CLpro and non-structural protein (NSP-12 with co-factors 7 and 8) trimer complex are used to study the protein-drug interactions with the phytochemicals from Ocimum Sanctum, Tinospora Cordifolia, Glycyrrhiza Glabra, and Azadirachta Indica. Which can give insight to be used as potent antiviral drugs against SARS-CoV-2. Twenty phytochemicals, five from each plant species, known for their wide range of biological activities were chosen from the literature. The in-silico study was carried out using virtual screening tools and the top five, which showed the least binding energies, were selected. Molecular docking tools revealed that gedunin and epoxy azadiradione proved to be excellent inhibitors for 3CLpro and so did Tinosporide for non-structural-protein complex. Further, the best-hit phytochemicals with respect to structure similarities with FDA drugs and investigatory drugs, were considered for comparative study. Molecular docking was done to check the drug-protein interactions and to check the inhibitory responses of these drugs against the viral protein. The analyses showed that the phytochemicals had similar responses on the protein complex but with exceptionally higher inhibitory responses hence which may be taken for further clinical study. 相似文献
6.
Ghoderao Karuna P. Jamble Shweta N. Kale Rohidas B. 《Journal of Solid State Electrochemistry》2019,23(6):1685-1695
Journal of Solid State Electrochemistry - Dye-sensitized solar cells (DSSCs) based on TiO2 nanostructures have attracted much attention due to their high photoconversion efficiency. Here, we report... 相似文献
7.
Shweta Bhagat Minhajul Arfeen Gourav Das Neha Patel Prasad V. Bharatam 《Journal of computational chemistry》2019,40(5):726-733
Carbocyclic carbenes (CCCs) are a class of nucleophilic carbenes which are very similar to N-heterocyclic carbenes (NHCs) in terms of their reactivity, but they do not contain a stabilizing heteroatom in their cyclic ring system. In this study, 17 representative known CCCs and 34 newly designed CCCs are evaluated using quantum chemical methods, and the results are compared in terms of their stability, nucleophilicity, and proton affinity (PA) parameters. The results are divided on the basis of ring size of the known and reported CCCs. The stability, nucleophilicity, PA, complexation energy, and bond strength–related parameters were estimated using M06/6-311++G(d,p) method. The results indicated that the CCCs known in the literature are strong σ-electron donating species and have considerable π-accepting properties. This study led to the design and identification of a few new CCCs with dimethylamine and diaminomethynyl substituents which can be singlet stable and are substantially nucleophilic. © 2018 Wiley Periodicals, Inc. 相似文献
8.
9.
Shweta J. Malode Jyothi C. Abbar Sharanappa T. Nandibewoor 《Monatshefte für Chemie / Chemical Monthly》2011,34(6):469-479
Abstract
The kinetics of the oxidation of ruthenium(III)-catalyzed oxidation of pentoxifylline (PTX) by diperiodatocuprate(III) (DPC) in aqueous alkaline medium at a constant ionic strength of 0.30 mol dm−3 was studied spectrophotometrically. The reaction between PTX and DPC in alkaline medium in the presence of Ru(III) exhibits 1:2 stoichiometry (PTX:DPC). The reaction was of first order in DPC, less than the unit order in [PTX] and [OH−] and negative fractional order in [IO4 −]. The order in [Ru(III)] was unity. Intervention of free radicals was observed in the reaction. The main products were identified by TLC and spectral studies including LC-MS. The oxidation reaction in alkaline medium has been shown to proceed via a Ru(III)-PTX complex, which reacts with monoperiodatocuprate(III) to decompose in a rate determining step followed by a fast step to give the products. The reaction constants involved in different steps of the mechanism were calculated. The activation parameters with respect to the slow step of the mechanism were computed and discussed, and thermodynamic quantities were also determined. The active species of catalyst and oxidant have been identified. 相似文献10.
Biswarup Chakraborty Shweta Kalra Rodrigo Beltrn‐Suito Chittaranjan Das Tim Hellmann Prashanth W. Menezes Matthias Driess 《化学:亚洲杂志》2020,15(6):852-859
In the urge of designing noble metal‐free and sustainable electrocatalysts for oxygen evolution reaction (OER), herein, a mineral Digenite Cu9S5 has been prepared from a molecular copper(I) precursor, [{(PyHS)2CuI(PyHS)}2](OTf)2 ( 1 ), and utilized as an anode material in electrocatalytic OER for the first time. A hot injection of 1 yielded a pure phase and highly crystalline Cu9S5, which was then electrophoretically deposited (EPD) on a highly conducting nickel foam (NF) substrate. When assessed as an electrode for OER, the Cu9S5/NF displayed an overpotential of merely 298±3 mV at a current density of 10 mA cm?2 in alkaline media. The overpotential recorded here supersedes the value obtained for the best reported Cu‐based as well as the benchmark precious‐metal‐based RuO2 and IrO2 electrocatalysts. In addition, the choronoamperometric OER indicated the superior stability of Cu9S5/NF, rendering its suitability as the sustainable anode material for practical feasibility. The excellent catalytic activity of Cu9S5 can be attributed to the formation of a crystalline CuO overlayer on the conductive Cu9S5 that behaves as active species to facilitate OER. This study delivers a distinct molecular precursor approach to produce highly active copper‐based catalysts that could be used as an efficient and durable OER electro(pre)catalysts relying on non‐precious metals. 相似文献