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A photoredox catalytic ensemble consisting of CuO‐Fe2O3 nanocomposites and oligomeric derivative of phenazine has been developed. The prepared system acts as an efficient photoredox catalyst for C?N bond formation reaction via SET mechanism under ‘green’ conditions (aerial environment, mixed aqueous media, recyclable), requiring less equivalents of base and amine substrate. The present study demonstrates the significant role of supramolecular assemblies as photooxidants and reductants upon irradiation and their important contribution towards the activation of the metallic centre through energy transfer and electron transfer pathways. The potential of oligomer 4 : CuO‐Fe2O3 has also been explored for C?C bond formation reactions via the Sonogashira protocol. 相似文献
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Polyaniline–graphene oxide nanocomposites: Influence of nonconducting graphene oxide on the conductivity and oxidation‐reduction mechanism of polyaniline 下载免费PDF全文
Vandana A. Mooss Anjali A. Athawale 《Journal of polymer science. Part A, Polymer chemistry》2016,54(23):3778-3786
The present endeavor focuses on the unusual interactions between polyaniline and graphene oxide (PANi–GO) which radically affects the properties of nanocomposites as it is an emerging material for many potential applications. A series of nanocomposites have been synthesized by varying the weight percentage of highly nonconducting GO with respect to aniline which exhibit superior properties in terms of shelf life, processability and conductivity due to the synergistic effect of GO and PANi. A comparison of the resistances of samples reveal that though as‐synthesized GO is insulating (80 MΩ), when added to PANi (283 kΩ) in small amounts yields conducting composites (50–280 Ω). Up to 5 weight % concentration, GO renders conductivity to the composite probably by increasing the doping level of PANi. Nonetheless, no further increase in conductivity observed on addition of more than 5 wt% GO in the composite has dictated us to unravel the structure property relationship between PANi and GO, where GO facilitates the formation of partially reduced phase of PANi, thereby restricting the electronic transport. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3778–3786 相似文献
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Radiofluorination of a Pre‐formed Gallium(III) Aza‐macrocyclic Complex: Towards Next‐Generation Positron Emission Tomography (PET) Imaging Agents 下载免费PDF全文
Dr. Rajiv Bhalla Prof. William Levason Dr. Sajinder K. Luthra Dr. Graeme McRobbie George Sanderson Prof. Gillian Reid 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(12):4688-4694
As part of a study to investigate the factors influencing the development of new, more effective metal‐complex‐based positron emission tomography (PET) imaging agents, the distorted octahedral complex, [GaCl(L)]?2 H2O has been prepared by reaction of 1‐benzyl‐1,4,7‐triazacyclononane‐4,7‐dicarboxylic acid hydrochloride (H2L?HCl) with Ga(NO3)3?9 H2O, which is a convenient source of GaIII for reactions in water. Spectroscopic and crystallographic data for [GaCl(L)]?2 H2O are described, together with the crystal structure of [GaCl(L)]?MeCN. Fluorination of this complex by Cl?/F? exchange was achieved in high yield by treatment with KF in water at room temperature over 90 minutes, although the reaction was complete in approximately 30 minutes if heated to 80 °C, giving [GaF(L)]?2 H2O in good yield. The same complex was obtained by hydrothermal synthesis from GaF3?3 H2O and Li2L, and has been characterised by single‐crystal X‐ray analysis, IR, 1H and 19F{1H} NMR spectroscopy and ESI+ MS. Radiofluorination of the pre‐formed [GaCl(L)]?2 H2O has been demonstrated on a 210 nanomolar scale in aqueous NaOAc at pH 4 by using carrier‐free 18F?, leading to 60–70 % 18F‐incorporation after heating to 80 °C for 30 minutes. The resulting radioproduct was purified easily by using a solid‐phase extraction (SPE) cartridge, leading to 98–99 % radiochemical purity. The [Ga18F(L)] is stable for at least 90 minutes in 10 % EtOH/NaOAc solution at pH 6, but defluorinates over this time scale at pH of approximately 7.5 in phosphate buffered saline (PBS) or human serum albumin (HSA). The subtle role of the Group 13 metal ion and co‐ligand donor set in influencing the pH dependence of this system is discussed in the context of developing potential new imaging agents for PET. 相似文献
5.
Tripathi Jai Prakash Jana Debaldev Vyshnavi Devi N. S. N. V. K. Tiwari Vandana Abbas Syed 《Nonlinear dynamics》2020,102(1):511-535
Nonlinear Dynamics - In this present study, we systematically explore the periodicity (almost periodic nature) of a dynamical system in time-varying environment, which portrays a special case of... 相似文献
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JPC – Journal of Planar Chromatography – Modern TLC - The present research work was aimed to determine the stability of cefprozil monohydrate (CEFZ) as per various stress degradation... 相似文献
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Andrew J. Guenthner Vandana Vij Timothy S. Haddad Josiah T. Reams Kevin R. Lamison Christopher M. Sahagun Sean M. Ramirez Gregory R. Yandek Suresh C. Suri Joseph M. Mabry 《Journal of polymer science. Part A, Polymer chemistry》2014,52(6):767-779
The synthesis and physical properties of new silicon‐containing polyfunctional cyanate ester monomers methyl[tris(4‐cyanatophenyl)]silane and tetrakis(4‐cyanatophenyl)silane, as well as polycyanurate networks formed from these monomers are reported. The higher crosslinking functionality compared to di(cyanate ester) monomers enables much higher ultimate glass transition temperatures to be obtained as a result of thermal cyclotrimerization. The ability to reach complete conversion is greatly enhanced by cocure of the new monomers with di(cyanate ester) monomers such as 1,1‐bis(4‐cyanatophenyl)ethane. The presence of silicon in these polycyanurate networks imparts improved resistance to rapid oxidation at elevated temperatures, resulting in char yields as high as 70% under nitrogen and 56% in air in the best‐performing networks. The water uptake in the silicon‐containing networks examined is 4–6 wt % after 96 h of immersion at 85 °C, considerably higher than both carbon‐containing and/or di(cyanate ester) analogs. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 767–779 相似文献
9.
A simple, isocratic, stability-indicating liquid chromatographic method for quantitative determination of curcumin was successfully developed. The chromatographic separations were achieved using a Hi-Q-Sil C18; 4.6 mm × 250 mm and 10 μm particle size column employing acetonitrile and acetate buffer (pH 3.0; 60: 40, v/v) as the mobile phase. The analyte was subjected to acidic, basic, oxidative, thermal and photo degradation. The method was validated with respect to linearity, precision, accuracy, limit of detection and limit of quantification. Curcumin was detected by UV-Vis detector at 425 nm whereas the degradation products were detected at 280 nm. The method was linear over the concentration range of 1–10 μg mL?1. The limit of detection was found to be 0.06 μg mL?1 and the quantification limit was 0.21 μg mL?1. Considerable degradation of the analyte was observed when it was subjected to alkaline conditions. Accuracy, evaluated as recovery, was in the range of 97–103%. Intra-day precision and intermediate precision showed relative standard deviations <1% and <2% respectively. 相似文献
10.
A proficient etiquette for the stereoselective synthesis of novel 3-methylthio-β-lactams and their Lewis acid mediated functionalization is described. Treatment of 2-methylthioethanoic acid and appropriate imines in the Staudinger reaction leads to the stereocontrolled synthesis of novel trans-3-methylthio-β-lactams in excellent yields. cis-3-Chloro-3-methylthio-β-lactams, obtained from stereoselective chlorination of trans-3-methylthio-β-lactams using N-chlorosuccinimide (NCS) and AIBN, were subjected to Lewis acid (TiCl4 or SnCl4) mediated functionalization using various active aromatic, heterocyclic and aliphatic compounds (nucleophiles). This reaction provides an easy access to novel, stereoselective cis-3-monosubstituted-3-methylthio-β-lactams, which further undergo smooth desulfurization with Raney-nickel to afford C-3 cis- and trans-monosubstituted-β-lactams. The cis or trans configuration of the hydrogen/chloro/nucleophile substituent at C-3 was assigned with respect to C4–H. 相似文献