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Supramolecular redox-responsive ferrocene hydrogels and microgels

Stimuli-responsive hydrogels have lately attracted a lot of attention in the chemistry and material fields because of the ?smart? change of their properties under outside stimuli including light, temperature, electric or magnetic field, pH, chemicals, shear stress, and redox reagents. Ferrocenyl (Fc) is often employed as a redox-responsive building unit due to its properties of chemical and electrochemical redox reversibility. This property involves reversible change between hydrophobicity and hydrophilicity, which endows hydrogels with unexpected features. Also, Fc derivatives are used as guest molecules featuring host?guest interactions with macrocyclic host molecules, mainly including cyclodextrins and pillararenes, commonly leading to the formation of supramolecular hydrogels with shape-memory, self-healing and sol?gel transition performances. This review focuses on the fabrication of various kinds of Fc-containing hydrogels and describes their gelling mechanisms, characteristic structures and properties, as well as functional applications. The review is divided into covalently cross-linked hydrogels and supramolecular cross-linked hydrogels. Furthermore, Fc-containing microgels constructed by chemically cross-linked three-dimensional polymer networks that are related to traditional hydrogels are also discussed. Fc-containing hydrogels and microgels are becoming more and more important as advanced functional materials, especially biomedical, shape-memory and self-healing materials.

Supramolecular redox-responsive ferrocene hydrogels and microgels

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Extended knowledge of 1273-86-5

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Electron transfer kinetics at oxide films on metallic biomaterials: Scanning electrochemical microscopy studies of Ti6AI4V

A native oxide film on the biphasic alloy Ti6Al4V was studied with scanning electrochemical microscopy (SECM). This alloy is commonly used for biomedical applications due to its biocompatibility and mechanical properties. The heterogeneously composed, n-semiconducting oxide film is of particular interest as biological systems are in contact only with these oxides and immunological rejection mechanisms may be connected to their electrochemical properties. Auger electron spectroscopy showed that the elemental composition of the oxide films on the alpha and Beta phase differ from each other. Approach curves were recorded above individual grains of the alpha phase in the feedback mode with several redox mediators. They were selected to cover a wide range of redox potentials for a better understanding of the surface kinetics of the oxide layer. The electron-transfer kinetics changed strongly depending on the redox potential of the mediator with respect to the energetic position of the bandgap of the oxide film. Predictions about the value of the flatband potential on an individual phase were derived from these experiments. Furthermore, SECM images were recorded to laterally resolve different electrochemical properties of the oxide film originating from the heterogeneous composition of the oxide on both phases.

Electron transfer kinetics at oxide films on metallic biomaterials: Scanning electrochemical microscopy studies of Ti6AI4V

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Properties and Exciting Facts About Vinylferrocene

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. category: iron-catalyst, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 1271-51-8, name is Vinylferrocene. In an article£¬Which mentioned a new discovery about 1271-51-8

The ?-Bonded Palladium(II) Complex of tetraphenylcyclobutadienecobalt(I)

tetraphenylcyclobutadienecobalt(I) reacts with lithium tetrachloropalladate(II) in the presence of sodium acetate to give an ortho-palladated binuclear complex.The ?-bonded structure of the complex was confirmed by studies of the IR and 1H-NMR spectra and of the reactions with triphenylphosphine, thalium(I) acetylacetonate, and lithium aluminum deuteride.The reactions of the ?-bonded complex with carbon monoxide and olefins have been examined.

The ?-Bonded Palladium(II) Complex of tetraphenylcyclobutadienecobalt(I)

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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1271-51-8, Name is Vinylferrocene, belongs to iron-catalyst compound, is a common compound. Formula: C12H3FeIn an article, once mentioned the new application about 1271-51-8.

Electronic structure and near-IR transitions of FcC2R and FcC4R dyads

This paper describes the orbital configuration which provides a basis for the understanding of the electronic structure and spectroscopic properties of 17e and 18e FcC2R and FcC4R dyads, where R is H, 1-naphthyl, 9-anthryl, 3-pyrenyl, perylenyl. DFT calculations show that destabilisation of the ferrocenyl pi orbitals upon binding a C{triple bond, long}CR group to a Cp ring leads to the metal-based a1 orbital dropping below the e1-a so that the frontier orbital configuration is (e2? -a, pi)2 (e2? -b,metal)2 (e1? -a, pi)2, (a1, metal)2. The contribution of the aryl group to the pi e2-a and e1-a orbitals varies with the annelation of the ring. The LUMO is aryl based. The calculations are consistent with the spectroscopic data for the 18e species. Oxidation to the 17e cations does not change the orbital configuration but the orbital energies are lowered by the positive charge centred on the Fe. A strongly solvatochromic transition in the near-IR, a signature for the 17e cations, is best described as an LMCT transition but the contribution of C2R and C4R to the donor and acceptor levels depends on the ionization energy of the aryl pi orbital. LMCT energies decrease from FcC2R to FcC4R dyads.

Electronic structure and near-IR transitions of FcC2R and FcC4R dyads

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Extracurricular laboratory:new discovery of Vinylferrocene

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Related Products of 1271-51-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1271-51-8, Name is Vinylferrocene, molecular formula is C12H3Fe. In a Article£¬once mentioned of 1271-51-8

A versatile electrochemical sensing receptor based on a molecularly imprinted polymer

Electrochemical molecularly imprinted polymers (e-MIPs) are reported for the first time. Their elaboration is based on the introduction of a redox tracer (vinylferrocene) inside the binding cavities of a cross-linked MIP. Determination of the analyte (benzo[a]pyrene) can be simply performed by measuring the redox tracer signal. the Partner Organisations 2014.

A versatile electrochemical sensing receptor based on a molecularly imprinted polymer

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Can You Really Do Chemisty Experiments About Ferrocenemethanol

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Mediated Fuel Cells: Soluble Redox Mediators and Their Applications to Electrochemical Reduction of O2 and Oxidation of H2, Alcohols, Biomass, and Complex Fuels

Mediated fuel cells are electrochemical devices that produce power in a manner similar to that of conventional proton exchange membrane fuel cells (PEMFCs). They differ from PEMFCs in their use of redox mediators dissolved in liquid electrolyte to conduct oxidation of the fuel or reduction of the oxidant, typically O2, in bulk solution. The mediators transport electrons (and often protons) between the electrode and the catalysts or chemical reagents in solution. This strategy can help overcome many of the challenges associated with conventional fuel cells, including managing complex multiphase reactions (as in O2 reduction) or the use of challenging or heterogeneous fuels, such as hydrocarbons, polyols, and biomass. Mediators are also commonly used in enzymatic fuel cells, where direct electron transfer from the electrode to the enzymatic active site can be slow. This review provides a comprehensive survey of historical and recent mediated fuel cell efforts, including applications using chemical and enzymatic catalysts.

Mediated Fuel Cells: Soluble Redox Mediators and Their Applications to Electrochemical Reduction of O2 and Oxidation of H2, Alcohols, Biomass, and Complex Fuels

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

The Absolute Best Science Experiment for 1271-48-3

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 1271-48-3, name is 1,1′-Ferrocenedicarboxaldehyde, introducing its new discovery. category: iron-catalyst

Ferrocene derivatives and its synthetic method and application (by machine translation)

The present invention provides two ferrocene pyridine derivative and its synthesis method, wherein ferrocene single arm pyridine derivatives FeL1 and ferrocene double-arm pyridine derivatives FeL2 can be used for Cu2 + And Cr3 + Detection. (by machine translation)

Ferrocene derivatives and its synthetic method and application (by machine translation)

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Final Thoughts on Chemistry for Vinylferrocene

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Cycloaddition of o-Carboryne with Vinyl Ethers: Synthesis of Carborane-Fused Cyclobutanes

o-Carboryne (1,2-dehydro-o-carborane) is a very useful synthon for the synthesis of a variety of carborane-functionalized molecules. Using 1-Li-2-OTf-o-C2B10H10 as a precursor, o-carboryne undergoes an efficient [2 + 2] cycloaddition with a large variety of vinyl ethers at room temperature to give a series of carborane-fused cyclobutanes in very good to high isolated yields. This reaction is compatible with many functional groups and has a very broad substrate scope ranging from alkyl- to aryl- and to silyl-substituted vinyl ethers. A stepwise reaction mechanism is proposed based on the control experiments, which is supported by DFT calculations. All new compounds have been fully characterized by 1H, 13C, and 11B NMR spectroscopy as well as HRMS spectrometry. Some are further confirmed by single-crystal X-ray analyses.

Cycloaddition of o-Carboryne with Vinyl Ethers: Synthesis of Carborane-Fused Cyclobutanes

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Archives for Chemistry Experiments of 1273-94-5

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, HPLC of Formula: C14H6FeO2, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1273-94-5, Name is 1,1′-Diacetylferrocene, molecular formula is C14H6FeO2

1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dion and Ferrocene-1,1?-bis(2,4-dioxobutanoic acid ethylester) as Ligands for transition metal ions. Crystal structure of Bis(1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dionato)copper(II)

The ligands 1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dion and ferrocene-1,1?-bis(2,4-dioxo-butanoic acid ethylester) have been prepared by reaction of acetylferrocene or 1,1?-diacetylferrocene and diethyl oxalate. They yield neutral chelates with CuII, NiII, ZnII, CoII, and MnII. The acid dissociation constants of the ligands and the stability constants of their metal complexes including FeII complexes are reported. The structure of bis(1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dionato)copper(II) was determined by X-ray structure analysis. A cis arrangement with a nearly square planar coordination sphere at the Cu atom is found.

1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dion and Ferrocene-1,1?-bis(2,4-dioxobutanoic acid ethylester) as Ligands for transition metal ions. Crystal structure of Bis(1-ethoxycarbonyl-3-ferrocenyl-propane-1,3-dionato)copper(II)

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

The Absolute Best Science Experiment for Hemin

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Heme Oxygenase Inhibition Sensitizes Neuroblastoma Cells to Carfilzomib

Neuroblastoma (NB) is an embryonic malignancy affecting the physiological development of adrenal medulla and paravertebral sympathetic ganglia in early infancy. Proteasome inhibitors (PIs) (i.e., carfilzomib (CFZ)) may represent a possible pharmacological treatment for solid tumors including NB. In the present study, we tested the effect of a novel non-competitive inhibitor of heme oxygenase-1 (HO-1), LS1/71, as a possible adjuvant therapy for the efficacy of CFZ in neuroblastoma cells. Our results showed that CFZ increased both HO-1 gene expression (about 18-fold) and HO activity (about 8-fold), following activation of the ER stress pathway. The involvement of HO-1 in CFZ-mediated cytotoxicity was further confirmed by the protective effect of pharmacological induction of HO-1, significantly attenuating cytotoxicity. In addition, HO-1 selective inhibition by a specific siRNA increased the cytotoxic effect following CFZ treatment in NB whereas SnMP, a competitive pharmacological inhibitor of HO, showed no changes in cytotoxicity. Our data suggest that treatment with CFZ produces ER stress in NB without activation of CHOP-mediated apoptosis, whereas co-treatment with CFZ and LS1/71 led to apoptosis activation and CHOP expression induction. In conclusion, our study showed that treatment with the non-competitive inhibitor of HO-1, LS1 / 71, increased cytotoxicity mediated by CFZ, triggering apoptosis following ER stress activation. These results suggest that PIs may represent a possible pharmacological treatment for solid tumors and that HO-1 inhibition may represent a possible strategy to overcome chemoresistance and increase the efficacy of chemotherapic regimens.

Heme Oxygenase Inhibition Sensitizes Neuroblastoma Cells to Carfilzomib

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion