Category: 16606-55-6

Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Wu, Fan, once mentioned the application of 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, molecular formula is C4H6O3, molecular weight is 102.09, MDL number is MFCD00798265, category is copper-catalyst. Now introduce a scientific discovery about this category, SDS of cas: 16606-55-6.

Highly dispersed boron-nitride/CuOx-supported Au nanoparticles for catalytic CO oxidation at low temperatures

Supported-Au catalysts show excellent activity in CO oxidation, where the nature of the support has a significant impact on catalytic activity. In this work, a hexagonal boron nitride (BN) support with a high surface area and adequately exposed edges was obtained by the ball-milling technique. Thereafter, impregnation of the BN support with Cu(NO3)(2) followed by calcination under air at 400 degrees C yielded a CuO-modified support. After Au loading, the obtained Au-CuOx/BN catalyst exhibited high CO oxidation activity at low temperatures with a 50% CO conversion temperature (T-50%) of 25 degrees C and a complete CO conversion temperature (T-100%) of 80 degrees C, well within the operational temperature range of proton exchange membrane fuel cells. However, the CO oxidation activity of Au/BN, prepared without CuOx for comparison, was found to be relatively low. Our study reveals that BN alone disperses both Cu and Au nanoparticles well. However, Au nanoparticles on the surface of BN in the absence of CuO species tend to aggregate upon CO oxidation reactions. Conversely, Au nanoparticles supported on the surface of CuO-modified BN remain small with an average size of similar to 2.0 nm before and after CO oxidation. Moreover, electron transfer between Au and Cu species possibly favors the stabilization of highly dispersed Au nanoparticles on the BN surface and also enhances CO adsorption. Thus, our results demonstrate that thermally stable and conductive CuO-modified BN is an excellent support for the preparation of highly dispersed and stable Au catalysts. (C) 2021, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

If you are interested in 16606-55-6, you can contact me at any time and look forward to more communication. SDS of cas: 16606-55-6.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology. 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, molecular formula is , belongs to copper-catalyst compound. In a document, author is Azuaje, Jhonny, Product Details of 16606-55-6.

Catalytic performance of a metal-free graphene oxide-Al2O3 composite assembled by 3D printing

This paper describes the first example of a 3D printed metal-free graphene oxide-Al2O3 (GO-Al2O3) catalytic system and evaluates its catalytic performance in model transformations. A new functional architecture creates synergies to combine the excellent catalytic effect and reaction scope of graphene oxide, the chemical stability and recyclability of the ceramic support, and the versatility and control over size of 3D printing technology. The graphene oxide-Al2O3 based catalyst presented here constitutes a step forward in the development of highly active, heterogeneous, and reusable ceramic catalysts.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 16606-55-6, in my other articles. Product Details of 16606-55-6.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, in an article , author is Liu, Lin-lin, once mentioned of 16606-55-6, Category: copper-catalyst.

Thermal reaction characteristics of paraffin in the presence of combustion catalysts

Paraffin fuels are regarded to be the best solid fuel of hybrid rocket motor due to the high regression rate, low cost, and environment friendly products. However, the regression rate of the fuels still cannot completely meet the requirement of the motor. Catocene, copper chromite, and cobalt stearate have been used as the combustion catalysts in this study, where the simultaneous TG-FTIR-MS and TG experiments at different heating rates were carried to investigate the thermal behavior of paraffin and paraffin/combustion catalysts mixtures. The results showed that both paraffin and the mixtures could decompose or be oxidized into gases products almost completely, with the main decomposition product of C2H6 and oxidation products of C2H4O, CO, CO2, and H2O. There was only one stage for both decomposition and oxidation of paraffin, and the kinetic model of decomposition process are close to two-dimensional diffusion (D2 model); cobalt stearate favored the decomposition of paraffin owing to the higher pre-exponential factor and the lower activation energy, whereas only copper chromite played an obvious positive role in both oxidation and regression rate of paraffin.

Interested yet? Read on for other articles about 16606-55-6, you can contact me at any time and look forward to more communication. Category: copper-catalyst.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Reference of 16606-55-6, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, belongs to copper-catalyst compound. In a article, author is Senthilkumar, Samuthirarajan, introduce new discover of the category.

A green approach for aerobic oxidation of benzylic alcohols catalysed by Cu-I-Y zeolite/TEMPO in ethanol without additional additives

An efficient and green protocol for aerobic oxidation of benzylic alcohols in ethanol using Cu-I-Y zeolite catalysts assisted by TEMPO (TEMPO = 2,2,6,6-tetramethyl-1-piperidine-N-oxyl) as the radical co-catalyst in the presence of atmospheric air under mild conditions is reported. The Cu-I-Y zeolite prepared via ion exchange between CuCl and HY zeolite was fully characterized by a variety of spectroscopic techniques including XRD, XPS, SEM, EDX and HRTEM. The incorporation of Cu(i) into the 3D-framework of the zeolite rendered the catalyst with good durability. The results of repetitive runs revealed that in the first three runs, there was hardly a decline in activity and a more substantial decrease in yield was observed afterwards, while the selectivity remained almost unchanged. The loss in activity was attributed to both the formation of CuO and the bleaching of copper into the liquid phase during the catalysis, of which the formation of CuO was believed to be the major contributor since the bleaching loss for each run was negligible (<2%). In this catalytic system, except TEMPO, no other additives were needed, either a base or a ligand, which was essential in some reported catalytic systems for the oxidation of alcohols. The aerobic oxidation proceeded under mild conditions (60 degrees C, and 18 hours) to quantitatively and selectively convert a wide range of benzylic alcohols to corresponding aldehydes, which shows great potential in developing green and environmentally benign catalysts for aerobic oxidation of alcohols. The system demonstrated excellent tolerance against electron-withdrawing groups on the phenyl ring of the alcohols and showed sensitivity to steric hindrance of the substrates, which is due to the confinement of the pores of the zeolite in which the oxidation occurred. Based on the mechanism reported in the literature for homogenous oxidation, a mechanism was analogously proposed for the aerobic oxidation of benzylic alcohols catalysed by this Cu(i)-containing zeolite catalyst. Reference of 16606-55-6, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 16606-55-6 is helpful to your research.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry, like all the natural sciences, Recommanded Product: (R)-4-Methyl-1,3-dioxolan-2-one, begins with the direct observation of nature¡ª in this case, of matter.16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, belongs to copper-catalyst compound. In a document, author is Song, Hui, introduce the new discover.

Copper-oxygen synergistic electronic reconstruction on g-C3N4 for efficient non-radical catalysis for peroxydisulfate and peroxymonosulfate

Due to the selectivity and environmental tolerance of non-radical reaction reactions, they have emerged as a promising way to treat special water bodies. Herein, we proposed a new non-radical reaction system that used a Cu and O co-doped g-C3N4 catalyst (CuO-CN) activated by peroxydisulfate (PDS) or peroxymonosulfate (PMS). In CuO-CN, Cu and O atoms were introduced into the structure of graphitic carbon nitride (g-C3N4) in an innovative configuration, resulting in a differentiated charge distribution around the Cu and O centres. The PDS/CuO-CN and PMS/CuO-CN systems could selectively degrade organic pollutants (e.g., bisphenol A, BPA) over a wide pH range (3-9), and the maximum BPA removal could reach 99%. For the PDS/CuO-CN system, the mechanism was hypothesized to involve the effective removal of BPA via electron transfer, and the PMS/CuO-CN system exploited the synergistic effect of singlet oxygen (O-1(2)) and electron transfer. This study describes a novel process for effective PMS or PDS activation by CuO-CN to efficiently degrade organic pollutants via a non-radical pathway.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 16606-55-6. Recommanded Product: (R)-4-Methyl-1,3-dioxolan-2-one.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Related Products of 16606-55-6, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, belongs to copper-catalyst compound. In a article, author is Dey, Avishek, introduce new discover of the category.

Cu2O/CuO heterojunction catalysts through atmospheric pressure plasma induced defect passivation

A novel route to fabricate Cu2 0/CuO heterojunction electrodes using an atmospheric pressure plasma jet (APPJ) is demonstrated. This process promotes favourable band alignment and produces nanoscale CuO surface features from Cu20 with low density of interfacial defects. This electrode can operate without any transparent current collector, showing remarkable currents and stability towards oxygen evolution reaction (OER) (6 mA cm(-2) for 2 h at pH14) as well as photocatalytic hydrogen evolution reaction (HER) activity (-1.9 mA cm(-2) for 800 s at pH7). When the electrocatalytic oxygen evolution (OER) activity was measured for Cu2O/CuO electrode deposited on FTO substrate the currents increased to similar to 40 mA cm(-2) at 0.8 V vs SCE in 1 M KOH without compensating for the electrode electrolyte surface resistance (iR correction). The composite films also exhibited a high rate towards photo degradation of Methylene Blue (MB) and phenol in the visible spectra, indicating efficient charge separation. We modelled the electronic structure of this epitaxially grown Cu2O/CuO heterojunction using density functional theory. The calculations revealed the distinctive shifts towards Fermi level of the p-band centre of O atom in Cu2O and d-band centre of Cu atom in CuO at the interface contribute towards the increased catalytic activity of the heterostructure. Another factor influencing the activity stems from the high density of excited species in the plasma introducing polar radicals at the electrode surface increasing the electrolyte coverage. This work presents the potential of APPJ functionalization to tune the surface electronic properties of copper oxide based catalysts for enhanced efficiency in OER and HER water splitting.

Related Products of 16606-55-6, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 16606-55-6 is helpful to your research.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, in an article , author is Bhargava Reddy, Mandapati, once mentioned of 16606-55-6, Recommanded Product: 16606-55-6.

Visible-light induced copper(i)-catalyzed oxidative cyclization of o-aminobenzamides with methanol and ethanol via HAT

The use of the in situ generated ligand-copper superoxo complex absorbing light energy to activate the alpha C(sp(3))-H of MeOH and EtOH via the hydrogen atom transfer (HAT) process for the synthesis of quinazolinones by oxidative cyclization of alcohols with o-aminobenzamide has been investigated. The synthetic utility of this protocol offers an efficient synthesis of a quinazolinone intermediate for erlotinb (anti-cancer agent) and 30 examples were reported.

Interested yet? Read on for other articles about 16606-55-6, you can contact me at any time and look forward to more communication. Recommanded Product: 16606-55-6.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

In an article, author is Amokrane, Samira, once mentioned the application of 16606-55-6, Application In Synthesis of (R)-4-Methyl-1,3-dioxolan-2-one, Name is (R)-4-Methyl-1,3-dioxolan-2-one, molecular formula is C4H6O3, molecular weight is 102.09, MDL number is MFCD00798265, category is copper-catalyst. Now introduce a scientific discovery about this category.

Effect of Adding Transition Metals to Copper on the Dehydrogenation Reaction of Ethanol

The present work aims to investigate the effect adding Ag, Co, Ni, Cd and Pt to copper on ethanol dehydrogenation. The catalysts synthesized by deposition-precipitation method were characterized using various physicochemical methods such as N-2 adsorption-desorption, TPR, SEM-EDX, XRD, XPS and TGA-DSC-MS. Catalytic evaluation results revealed that the predominant product of the reaction was acetaldehyde. Monometallic copper or mixed with Cd, Ag or Co show good catalytic performances. Adding nickel to copper improves the process conversion but reduces acetaldehyde selectivity, giving rise to methane in produced hydrogen. Pt-Cu/SiO2 catalyst guides the reaction towards diethyl ether. Time on stream tests performed during 12 h at 260 degrees C, showed that adding Cd to Cu enhances its stability by over 30% of conversion, this is explained by the reduction of copper crystallites sintering, which makes Cd-Cu/SiO2 a promising catalyst for the production of acetaldehyde by ethanol dehydrogenation.

If you are interested in 16606-55-6, you can contact me at any time and look forward to more communication. Application In Synthesis of (R)-4-Methyl-1,3-dioxolan-2-one.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry, like all the natural sciences, Application In Synthesis of (R)-4-Methyl-1,3-dioxolan-2-one, begins with the direct observation of nature¡ª in this case, of matter.16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, belongs to copper-catalyst compound. In a document, author is Yang, Lixia, introduce the new discover.

Self-assembly Cu2O nanowire arrays on Cu mesh: A solid-state, highly-efficient, and stable photocatalyst for toluene degradation under sunlight

Sunlight driven photocatalysis offers an effective and eco-friendly technology for volatile organic compounds (VOCs) removal. Three dimensional (3D) and oriented structure can facilitate efficient photon absorption and rapid diffusion of VOCs, which prevails over the powder-formed catalysts. Herein, free-standing and uniform p-type Cu2O nanowire (NW) arrays were obtained through heat treatment of Cu(OH)(2) NWs, which were spontaneously grown from Cu mesh in air under room temperature for the first time. The as-prepared Cu2O NWs show excellent degradation performance in decomposing 30 ppm toluene (99.9 % within 120 min) and high stability (no decline after ten recycles). The toluene degradation was also conducted under the natural sunlight, demonstrating complete removal from 12:00 am to 15:00 pm. During photocatalysis, toluene is attacked by the photogenerated holes (h(+)) and hydroxyl radicals (center dot OH), and finally oxidized to nontoxic small molecules. The photocatalytic removing toluene with Cu2O NWs/Cu mesh has a promising application prospect owing to its low cost, high efficiency, stability, and convenient operation.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 16606-55-6. Application In Synthesis of (R)-4-Methyl-1,3-dioxolan-2-one.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry, like all the natural sciences, Safety of (R)-4-Methyl-1,3-dioxolan-2-one, begins with the direct observation of nature¡ª in this case, of matter.16606-55-6, Name is (R)-4-Methyl-1,3-dioxolan-2-one, SMILES is O=C1OC[C@@H](C)O1, belongs to copper-catalyst compound. In a document, author is Feng, Zhen, introduce the new discover.

Theoretical investigation of CO2 electroreduction on N (B)-doped graphdiyne mononlayer supported single copper atom

Carbon dioxide electrochemical reduction reaction (CO2RR) with proton-electron pair delineates an intriguing prospect for converting CO2 to useful chemicals. However, CO2RR is urgently required low-cost and high efficient electrocatalysts to overcome the sluggish reaction kinetic and ultralow selectivity. Here by means of firstprinciple computations, the geometric constructions, electronic structures, and CO2RR catalytic performance of boron- and nitrogen-doped graphdiyne anchoring a single Cu atom (Cu@N-doped GDY and Cu@B-doped GDY) were systematically investigated. These eight Cu@doped GDY complexes possess excellent stability. The adsorption free energies showed that the eight Cu@doped GDY could spontaneously capture CO2 molecules. The Cu@N-doped GDY monolayers exhibit a more efficient catalytic performance for CO2 reduction compared to Cu@B-doped GDY because of the differences in adsorption energies and charge transfer. The calculations further indicated that the Cu@Nb-doped GDY complex possesses excellent catalytic character toward CO2RR with the same limiting potentials of -0.65 V for production of HCOOH, CO, OCH2, CH3OH, and CH4. Charge analysis indicated that the *OCHO and *COOH species gain more electrons from Cu@N-doped GDY than from Cu@Bdoped GDY complexes due to different electronegativity of coordinated element. Our findings highlighted the electronegativity of coordinated elements for the design of atomic metal catalysts.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 16606-55-6. Safety of (R)-4-Methyl-1,3-dioxolan-2-one.

Reference:
Copper catalysis in organic synthesis – NCBI,
,Special Issue “Fundamentals and Applications of Copper-Based Catalysts”