Wang, Zhen’s team published research in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2019 | CAS: 13395-16-9

Bis(acetylacetone)copper(cas: 13395-16-9) catalyzes coupling and carbene transfer reactions. Metal acetylacetonates are used as catalysts for polymerization of olefins and transesterification. Application of 13395-16-9

The author of 《The controllable growth of PtCuRh rhombic dodecahedral nanoframes as efficient catalysts for alcohol electrochemical oxidation》 were Wang, Zhen; Huang, Lei; Tian, Zhi Qun; Shen, Pei Kang. And the article was published in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2019. Application of 13395-16-9 The author mentioned the following in the article:

Platinum-based catalysts with heterogeneous structures, such as three-dimensional (3D) nanoframes and highly branched architectures, have broad application prospects due to their fully accessible surfaces and high atom utilization. However, the fragile frames and dendrites with high energy easily suffer from structural collapse during catalytic processes. Hence, we synthesized Rh-strengthened PtCuRh rhombohedral dodecahedrons with nanodendrites (RDD) through a one-pot solvothermal method, which could be etched to obtain totally open nanoframe PtCuRh rhombohedral dodecahedrons with nanodendrites (RDND). More interestingly, the growth of the nanodendrites can be easily controlled through changing the reaction temperature Meanwhile, the length of the nanodendrites can be controlled through adjusting the amount of CTAB and the reaction time. In addition, synergistic effects between Pt, Cu and Rh modified the electronic structure; in particular Rh metal oxide on the surface contributes heavily towards improving the electrocatalytic efficiency. Therefore the as-prepared catalyst PtCuRh RDND shows superior catalytic performance towards the methanol oxidation reaction (MOR) as well as the ethanol oxidation reaction (EOR) compared to TKK-com. Pt/C. Remarkably, after 1000 electrochem. cycles of the MOR, the superior mass activity of PtCuRh RDND surpasses that of TKK-com. Pt/C by 2.6 times, benefiting from enhanced CO tolerance and the stable structure. This work provides a facile and feasible strategy for synthesizing stable and efficient nanoframe catalysts. In the part of experimental materials, we found many familiar compounds, such as Bis(acetylacetone)copper(cas: 13395-16-9Application of 13395-16-9)

Bis(acetylacetone)copper(cas: 13395-16-9) catalyzes coupling and carbene transfer reactions. Metal acetylacetonates are used as catalysts for polymerization of olefins and transesterification. Application of 13395-16-9

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

 

Li, Menggang’s team published research in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2019 | CAS: 13395-16-9

Bis(acetylacetone)copper(cas: 13395-16-9) is used as PVC stabilizer, and curing agents for epoxy resins, acrylic adhesives and silicone rubbers. It is also used as solvents, lubricant additives, paint drier, and pesticides.Quality Control of Bis(acetylacetone)copper

The author of 《Modulating the surface segregation of PdCuRu nanocrystals for enhanced all-pH hydrogen evolution electrocatalysis》 were Li, Menggang; Luo, Mingchuan; Xia, Zhonghong; Yang, Yong; Huang, Yarong; Wu, Dong; Sun, Yingjun; Li, Chunji; Chao, Yuguang; Yang, Wenxiu; Yang, Weiwei; Yu, Yongsheng; Guo, Shaojun. And the article was published in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2019. Quality Control of Bis(acetylacetone)copper The author mentioned the following in the article:

Core-shell architecture coupled with rational surface engineering constitutes an efficient strategy for promoting electrocatalysis on multimetallic nanocrystals via the optimization of composition, facets and coordination environment. Here, by leveraging controlled surface segregation, we realize core-shell formation with systematic tuning of surface composition on well-defined PdCuRu nanocrystals. When applied for the hydrogen evolution reaction (HER), we established a direct correlation between surface composition and activity. In particular, PdCuRu catalysts with a Pd-rich surface achieved an overpotential of 31 mV at a c.d. of 10 mA cm-2 and a low Tafel slope of 52 mV dec-1 in an alk. electrolyte, considerably enhanced relative to control PdCuRu/C catalysts with other surface compositions and even exceeding those of state-of-the-art Pt/C. Similar trends were also observed in both neutral and acid electrolytes. We deduce that, in this catalytic system, the enhanced electrocatalysis originates from the strain effect rather than the bifunctional mechanism. The present study builds a bridge between surface engineering and HER performance, and opens up new material designs for surface Pd-rich core-shell nanostructures for the purpose of improving HER catalytic activity and stability at all pH values. In addition to this study using Bis(acetylacetone)copper, there are many other studies that have used Bis(acetylacetone)copper(cas: 13395-16-9Quality Control of Bis(acetylacetone)copper) was used in this study.

Bis(acetylacetone)copper(cas: 13395-16-9) is used as PVC stabilizer, and curing agents for epoxy resins, acrylic adhesives and silicone rubbers. It is also used as solvents, lubricant additives, paint drier, and pesticides.Quality Control of Bis(acetylacetone)copper

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

 

Assoumatine, Tokoure’s team published research in Acta Crystallographica, Section E: Crystallographic Communications in 2020 | CAS: 7789-45-9

Some reported applications of Cupric bromide(cas: 7789-45-9) are: catalyst in cross coupling reactions; co-catalyst in Sonogashira coupling; lewis acid in enantioselective addition of alkynes.SDS of cas: 7789-45-9

《Crystal structures of [(μ2-L1)dibromidodicopper(II)] dibromide and poly[[(μ2-L1)diiodidodicopper(I)]-di-μ-iodido-dicopper(I)], where L1 is 2,5,8,11,14,17-hexathia-[9.9](2,6,3,5)-pyrazinophane》 was published in Acta Crystallographica, Section E: Crystallographic Communications in 2020. These research results belong to Assoumatine, Tokoure; Stoeckli-Evans, Helen. SDS of cas: 7789-45-9 The article mentions the following:

The reaction of the hexathiapyrazinophane ligand, 2,5,8,11,14,17-hexathia-[9.9](2,6,3,5)-pyrazinophane (L1), with copper(II) dibromide led to the formation of a binuclear complex, [μ2-2,5,8,11,14,17-hexathia-[9.9](2,6,3,5)-pyrazinophane]bis[bromidocopper(II)] dibromide, [Cu2Br2(C16H24N2S6)]Br2, (I). The complex possesses inversion symmetry with the pyrazine ring being situated about a center of symmetry. The ligand coordinates to the copper(II) atom in a bis-tetradentate manner and the copper atom has a fivefold NS3Br coordination environment with a distorted shape. The reaction of ligand L1 with copper(I) iodide also gave a binuclear complex, which is bridged by a Cu2I2 unit to form a two-dimensional coordination polymer, poly[[μ2-2,5,8,11,14,17-hexathia-[9.9](2,6,3,5)-pyrazinophane]tetra-μ-iodido-tetracopper(I)], [Cu4I4(C16H24N2S6)]n, (II). The binuclear unit possesses inversion symmetry with the pyrazine ring being located about a center of symmetry. The Cu2I2 unit is also located about an inversion center. The two independent copper(I) atoms are both fourfold coordinate. That coordinating to the ligand L1 in a bis-tridentate manner has an NS2I coordination environment and an irregular shape, while the second copper(I) atom, where L1 coordinates in a bis-monodentate manner, has an SI3 coordination environment with an almost perfect tetrahedral geometry. In the crystal of I, the cations and Br- anions are linked by a number of C-H···S and C-H···Br hydrogen bonds, forming a supramol. network. In the crystal of II, the two-dimensional coordination polymers lie parallel to the ab plane and there are no significant inter-layer contacts present. After reading the article, we found that the author used Cupric bromide(cas: 7789-45-9SDS of cas: 7789-45-9)

Some reported applications of Cupric bromide(cas: 7789-45-9) are: catalyst in cross coupling reactions; co-catalyst in Sonogashira coupling; lewis acid in enantioselective addition of alkynes.SDS of cas: 7789-45-9

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

 

Sui, Yan’s team published research in Journal of Materials Chemistry C: Materials for Optical and Electronic Devices in 2019 | CAS: 7789-45-9

Some reported applications of Cupric bromide(cas: 7789-45-9) are: catalyst in cross coupling reactions; co-catalyst in Sonogashira coupling; lewis acid in enantioselective addition of alkynes.Formula: Br2Cu

Formula: Br2CuIn 2019 ,《A semiconducting organic-inorganic hybrid ([BrCH2CH2N(CH3)3]2+[CuBr4]2-) with switchable dielectric properties derived from an unusual piston-like displacive movement》 was published in Journal of Materials Chemistry C: Materials for Optical and Electronic Devices. The article was written by Sui, Yan; Zhong, Ye-Shun; Wang, Jing-Jing; Xia, Qin; Wang, Liang-Jun; Liu, Dong-Sheng. The article contains the following contents:

According to quasi-spherical theory, structural modifications of spherical organic components are useful in obtaining ferroelec. or switchable dielec. organic-inorganic hybrid compounds, but how to tailor the spherical organic components is still unclear. In the current work, a prototype spherical Me4N+ cation was modified by replacing one of its H atoms with a CH2Br group, rather than with the widely studied Br atom, to obtain a new organic-inorganic hybrid compound, [BrCH2CH2NMe3]2+[CuBr4]2- (BETABCuBr). The structure, phase transition, and dielec. and optical properties of BETABCuBr were carefully characterized. Based on these results, BETABCuBr was indicated to undergo a reversible phase transition at ∼356 K, mainly due to a piston-like displacive movement of its Cu atom. The extension of the C chain was concluded to lead to a change of the phase transition mechanism from the typical order-disorder movement to an unusual displacive movement. The authors expect the results of this work to contribute to the exploration of new types of phase transition materials. After reading the article, we found that the author used Cupric bromide(cas: 7789-45-9Formula: Br2Cu)

Some reported applications of Cupric bromide(cas: 7789-45-9) are: catalyst in cross coupling reactions; co-catalyst in Sonogashira coupling; lewis acid in enantioselective addition of alkynes.Formula: Br2Cu

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

 

Bates, Morgan W.’s team published research in Proceedings of the National Academy of Sciences of the United States of America in 2019 | CAS: 7789-45-9

Cupric bromide(cas: 7789-45-9) can be used as reducing agent, when complexed by three molecules of pyridine initiators for the controlled polymerization of styrene, methyl acrylate and methyl methacrylate.Application In Synthesis of Cupric bromide

In 2019,Proceedings of the National Academy of Sciences of the United States of America included an article by Bates, Morgan W.; Lequieu, Joshua; Barbon, Stephanie M.; Lewis, Ronald M. III; Delaney, Kris T.; Anastasaki, Athina; Hawker, Craig J.; Fredrickson, Glenn H.; Bates, Christopher M.. Application In Synthesis of Cupric bromide. The article was titled 《Stability of the A15 phase in diblock copolymer melts》. The information in the text is summarized as follows:

The self-assembly of block polymers into well-ordered nanostructures underpins their utility across fundamental and applied polymer science, yet only a handful of equilibrium morphologies are known with the simplest AB-type materials. Here, we report the discovery of the A15 sphere phase in single-component diblock copolymer melts comprising poly(dodecyl acrylate)-block-poly(lactide). A systematic exploration of phase space revealed that A15 forms across a substantial range of minority lactide block volume fractions (fL = 0.25 – 0.33) situated between the σ-sphere phase and hexagonally close-packed cylinders. SCF theory rationalizes the thermodn. stability of A15 as a consequence of extreme conformational asymmetry. The exptl. observed A15-disorder phase transition is not captured using mean-field approximations but instead arises due to composition fluctuations as evidenced by fully fluctuating field-theoretic simulations. This combination of experiments and field-theoretic simulations provides rational design rules that can be used to generate unique, polymer-based mesophases through self-assembly. After reading the article, we found that the author used Cupric bromide(cas: 7789-45-9Application In Synthesis of Cupric bromide)

Cupric bromide(cas: 7789-45-9) can be used as reducing agent, when complexed by three molecules of pyridine initiators for the controlled polymerization of styrene, methyl acrylate and methyl methacrylate.Application In Synthesis of Cupric bromide

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

 

Extended knowledge of 676525-77-2

《Light-Mediated Reductive Debromination of Unactivated Alkyl and Aryl Bromides》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound([Ir(dtbbpy)(ppy)2]PF6)Safety of [Ir(dtbbpy)(ppy)2]PF6.

Devery, James J.; Nguyen, John D.; Dai, Chunhui; Stephenson, Corey R. J. published an article about the compound: [Ir(dtbbpy)(ppy)2]PF6( cas:676525-77-2,SMILESS:[F-][P+5]([F-])([F-])([F-])([F-])[F-].CC(C)(C1=CC=[N]([Ir+3]23([C-]4=CC=CC=C4C5=CC=CC=[N]25)([C-]6=CC=CC=C6C7=CC=CC=[N]37)[N]8=CC=C(C(C)(C)C)C=C98)C9=C1)C ).Safety of [Ir(dtbbpy)(ppy)2]PF6. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:676525-77-2) through the article.

Cleavage of carbon-halogen bonds via either single-electron reduction or atom transfer is a powerful transformation in the construction of complex mols. In particular, mild, selective hydrodehalogenations provide an excellent follow-up to the application of halogen atoms as directing groups or the utilization of atom transfer radical addition (ATRA) chem. for the production of hydrocarbons. Here we combine the mechanistic properties of photoredox catalysis and silane-mediated atom transfer chem. to accomplish the hydrodebromination of carbon-bromide bonds. The resulting method is performed under visible light irradiation in an open vessel and is capable of the efficient reduction of a variety of unactivated alkyl and aryl substrates.

《Light-Mediated Reductive Debromination of Unactivated Alkyl and Aryl Bromides》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound([Ir(dtbbpy)(ppy)2]PF6)Safety of [Ir(dtbbpy)(ppy)2]PF6.

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

 

New learning discoveries about 20859-23-8

《Highly enantioselective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound((S)-2-Bromosuccinic acid)Electric Literature of C4H5BrO4.

Electric Literature of C4H5BrO4. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (S)-2-Bromosuccinic acid, is researched, Molecular C4H5BrO4, CAS is 20859-23-8, about Highly enantioselective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase. Author is Ekborg-Ott, K.; Liu, Youbang; Armstrong, Daniel W..

The macrocyclic glycopeptide, ristocetin A, was covalently bonded to a silica gel support and evaluated as a liquid chromatog. (LC) chiral stationary phase (CSP). Over 230 racemates were resolved in either the reversed-phase mode, the normal-phase mode, or the polar-organic mode. The retention behavior and selectivity of this CSP were examined in each mode. Optimization of separations on this column is discussed. The ristocetin A CSP appeared to be complimentary to other glycopeptide CSPs (i.e., vancomycin and teicoplanin). Column stability was excellent. The CSP was not irreversibly altered when going from one mobile phase mode to another.

《Highly enantioselective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound((S)-2-Bromosuccinic acid)Electric Literature of C4H5BrO4.

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

 

Awesome and Easy Science Experiments about 676525-77-2

《Catalytic Olefin Hydroamination with Aminium Radical Cations: A Photoredox Method for Direct C-N Bond Formation》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound([Ir(dtbbpy)(ppy)2]PF6)Related Products of 676525-77-2.

Related Products of 676525-77-2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: [Ir(dtbbpy)(ppy)2]PF6, is researched, Molecular C40H40F6IrN4P, CAS is 676525-77-2, about Catalytic Olefin Hydroamination with Aminium Radical Cations: A Photoredox Method for Direct C-N Bond Formation. Author is Musacchio, Andrew J.; Nguyen, Lucas Q.; Beard, G. Hudson; Knowles, Robert R..

While olefin amination with aminium radical cations is a classical method for C-N bond formation, catalytic variants that utilize simple 2° amine precursors remain largely undeveloped. Herein we report a new visible-light photoredox protocol for the intramol. anti-Markovnikov hydroamination of aryl olefins that proceeds through catalytically generated aminium radical intermediates. Mechanistic studies are consistent with a process involving amine oxidation via electron transfer, turnover-limiting C-N bond formation, and a second electron transfer step to reduce a carbon-centered radical, rendering the overall process redox-neutral. A range of structurally diverse N-aryl heterocycles can be prepared in good to excellent yields under conditions significantly milder than those required by conventional aminium-based protocols.

《Catalytic Olefin Hydroamination with Aminium Radical Cations: A Photoredox Method for Direct C-N Bond Formation》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound([Ir(dtbbpy)(ppy)2]PF6)Related Products of 676525-77-2.

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

 

Decrypt The Mystery Of 89396-94-1

《Kinetics of degradation of imidapril hydrochloride in finished dosage formulations》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound((S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride)Category: copper-catalyst.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Kinetics of degradation of imidapril hydrochloride in finished dosage formulations, published in 2013-08-31, which mentions a compound: 89396-94-1, mainly applied to imidapril hydrochloride tablet stability degradability HPLC, Category: copper-catalyst.

This study investigates the impact of relative air humidity and temperature on the stability of imidapril hydrochloride (IMD) tablets. For this purpose the forced degradation test was used and the following environmental conditions were employed: RH = 76.4% and the temperature range of 313 – 333 K. For the determination of IMD content in the analyzed samples a reversed-phase high performance liquid chromatog. (RP-HPLC) technique was used. Three series of tablets were prepared: whole-blistered tablets, whole-bare tablets and halved-bare tablets, in order to analyze the influence of different in-home storage habits on IMD tablets’ quality. In the course of the study, the degradation of IMD was observed in each series of tablets. The kinetic mechanisms and the thermodn. parameters of these reactions were established. It was evidenced that halved IMD tablets stored without immediate packaging retain their quality only for 12 days while tablets stored according to label recommendations are stable for 513 days.

《Kinetics of degradation of imidapril hydrochloride in finished dosage formulations》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound((S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride)Category: copper-catalyst.

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

 

Properties and Exciting Facts About 14898-67-0

《Redox Stability Controls the Cellular Uptake and Activity of Ruthenium-Based Inhibitors of the Mitochondrial Calcium Uniporter (MCU)》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Ruthenium(III) chloride xhydrate)Product Details of 14898-67-0.

Product Details of 14898-67-0. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Ruthenium(III) chloride xhydrate, is researched, Molecular Cl3H2ORu, CAS is 14898-67-0, about Redox Stability Controls the Cellular Uptake and Activity of Ruthenium-Based Inhibitors of the Mitochondrial Calcium Uniporter (MCU). Author is Woods, Joshua J.; Lovett, James; Lai, Barry; Harris, Hugh H.; Wilson, Justin J..

The mitochondrial calcium uniporter (MCU) is the ion channel that mediates Ca2+ uptake in mitochondria. Inhibitors of the MCU are valuable as potential therapeutic agents and tools to study mitochondrial Ca2+. The best-known inhibitor of the MCU is the ruthenium compound Ru360. Although this compound is effective in permeabilized cells, it does not work in intact biol. systems. We have recently reported the synthesis and characterization of Ru265, a complex that selectively inhibits the MCU in intact cells. Here, the phys. and biol. properties of Ru265 and Ru360 are described in detail. Using at. absorption spectroscopy and X-ray fluorescence imaging, we show that Ru265 is transported by organic cation transporter 3 (OCT3) and taken up more effectively than Ru360. As an explanation for the poor cell uptake of Ru360, we show that Ru360 is deactivated by biol. reductants. These data highlight how structural modifications in metal complexes can have profound effects on their biol. activities.

《Redox Stability Controls the Cellular Uptake and Activity of Ruthenium-Based Inhibitors of the Mitochondrial Calcium Uniporter (MCU)》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Ruthenium(III) chloride xhydrate)Product Details of 14898-67-0.

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