In the present study,a plasma-electrochemical method was demonstrated for the synthesis of europium doped ceria ***(NO3)3· 6H2O and Eu(NO3)3·5H2O were used as the starting materials and being dissolved in th...
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In the present study,a plasma-electrochemical method was demonstrated for the synthesis of europium doped ceria ***(NO3)3· 6H2O and Eu(NO3)3·5H2O were used as the starting materials and being dissolved in the distilled water as the electrolyte *** plasma-liquid interaction process was in-situ investigated by an optical emission spectroscopy,and the obtained products were characterized by complementary analytical *** showed that crystalline cubic CeO2:Eu3+ nanoparticles were successfully obtained,with a particle size in the range from 30 to 60 *** crystal structure didn't change during the calcination at a temperature from 400℃ to 1000℃,with the average erystallite size being estimated to be 52 nm at 1000℃.Eu3+ ions were shown to be effectively and uniformly doped into the CeO2 *** a result,the obtained nanophosphors emit apparent red color under the UV irradiation,which can be easily observed by naked *** photoluminescence spectrum further proves the downshift behavior of the obtained products,where characteristic 5Do → 7F1,2,3 transitions of Eu3+ ions had been *** to the simple,flexible and environmental friendly process,this plasma-electrochemical method should have great potential for the synthesis of a series of nanophosphors,especially for bio-application purpose.
Continuous-flowmicroreactor technology has been embraced by researchers in academia and industry due to its excellent transport properties and the increased safety and control over challenging chemical transformation...
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Photocatalysis for small-molecule activation has advanced considerably over the past decade, yet its scale-up remains challenging in part due to photon attenuation effects. One promising solution lies in combining hig...
Photocatalysis for small-molecule activation has advanced considerably over the past decade, yet its scale-up remains challenging in part due to photon attenuation effects. One promising solution lies in combining high photonic intensities with continuous-flow reactor technology, requiring careful understanding of photon transport for successful implementation. Here, to address this, we introduce a characterization approach, starting with radiometric light source analysis, followed by three-dimensional reactor and light source simulation. This strategy, when followed up with chemical actinometry experiments, decouples photon flux quantification and path length determination, substantially curtailing the experimental process. The workflow proves versatile across various reactor systems, simplifying intricate light interactions into a single one-dimensional parameter—the effective optical path length. This parameter effectively characterizes photoreactor setups, irrespective of scale, geometry, light intensity or concentration. Additionally, the proposed workflow provides insight into light source positioning and reactor design, and facilitates experiments at lower concentrations, ensuring representative reactor operation. In essence, our approach provides a thorough, efficient and consistent framework for reactor irradiation characterization.
A continuous‐flow, visible‐light‐promoted method has been developed to overcome the limitations of iron‐catalyzed Kumada–Corriu cross‐coupling reactions. A variety of strongly electron rich aryl chlorides, previ...
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A continuous‐flow, visible‐light‐promoted method has been developed to overcome the limitations of iron‐catalyzed Kumada–Corriu cross‐coupling reactions. A variety of strongly electron rich aryl chlorides, previously hardly reactive, could be efficiently coupled with aliphatic Grignard reagents at room temperature in high yields and within a few minutes’ residence time, considerably enhancing the applicability of this iron‐catalyzed reaction. The robustness of this protocol was demonstrated on a multigram scale, thus providing the potential for future pharmaceutical application.
A mild and selective C(sp 3 )−H aerobic oxidation enabled by decatungstate photocatalysis has been developed. The reaction can be significantly improved in a microflow reactor enabling the safe use of oxygen and enhan...
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A mild and selective C(sp 3 )−H aerobic oxidation enabled by decatungstate photocatalysis has been developed. The reaction can be significantly improved in a microflow reactor enabling the safe use of oxygen and enhanced irradiation of the reaction mixture. Our method allows for the oxidation of both activated and unactivated C−H bonds (30 examples). The ability to selectively oxidize natural scaffolds, such as (−)‐ambroxide, pregnenolone acetate, (+)‐sclareolide, and artemisinin, exemplifies the utility of this new method.
Styrenes represent a challenging class of substrates for current radical trifluoromethylation and hydrotrifluoromethylation methods due to a myriad of potential side reactions. Herein, we describe the development of m...
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Styrenes represent a challenging class of substrates for current radical trifluoromethylation and hydrotrifluoromethylation methods due to a myriad of potential side reactions. Herein, we describe the development of mild, selective and broadly applicable photocatalytic trifluoromethylation and hydrotrifluoromethylation protocols for these challenging substrates. The methods use fac‐Ir(ppy) 3 , visible light and inexpensive CF 3 I and can be applied to a diverse set of vinylarene substrates. The use of continuous‐flow photochemical reaction conditions allowed to reduce the reaction time and increase the reaction selectivity.
The use of solar light to promote chemical reactions holds significant potential with regard to sustainable energy solutions. While the number of visible light‐induced transformations has increased significantly, the...
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The use of solar light to promote chemical reactions holds significant potential with regard to sustainable energy solutions. While the number of visible light‐induced transformations has increased significantly, the use of abundant solar light has been extremely limited. We report a leaf‐inspired photomicroreactor that constitutes a merger between luminescent solar concentrators (LSCs) and flow photochemistry to enable green and efficient reactions powered by solar irradiation. This device based on fluorescent dye‐doped polydimethylsiloxane collects sunlight, focuses the energy to a narrow wavelength region, and then transports that energy to embedded microchannels where the flowing reactants are converted.
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