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A typical Chinese liquor was characterised using a triple-electrode system with clean and simple design. In this approach, liquors were analysed with no other pre-treatment than mixing the liquor with a potassium chloride solution to ensure sufficient conductivity. Two broad reduction peaks at [?0.3 V, ?0.5 V] and [?0.7 V, ?0.8 V] were present in the cyclic voltammetry, demonstrating the feasibility of the gold electrode for liquor characterisation. Both the competing reactions in the liquor samples contributed to the reduction current. Thus, the steady-state microelectrode voltammetry affords an opportunity to estimate the total concentration of the redox-active species in the mixed compounds according to the relationship between the total concentration and the value of limiting diffusion current. Further, the discrimination of liquors at different ageing times was realised by the conjunction of the electrochemical results and principal component analysis.

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Reference:
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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Indolin-2-one (oxindole), (I), undergoes a Knoevenagel con-densation with ferrocene-1,1?-dicarb-aldehyde, (II), to afford the title complex 3,3?-[(E,E)-ferrocene-1,1?-diyl-di-methyl-idyne]diindolin-2-one dichloro-methane disolvate, [Fe(C28H20N2O 2)]·2CH2Cl2, (IV). The structure of (IV) contains two ferrocene complex molecules in the asymmetric unit and displays, as expected, inter-molecular hydrogen bonding (N-H…O=C) between the indolin-2-one units. Inter-molecular pi-pi stacking inter-actions are also observed.

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Reference:
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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The topic of intermolecular interactions enhancing electron tunneling between protein residues on biofilm surface has been investigated by some theoretical studies. However, few of experimental studies could confirm this viewpoint. In this work, the Mercaptopropionic acid self-assembled monolayer (MPA SAM) with terminal carboxyl groups was constructed, as a simplified model for functionalized biomimic membrane. The electron tunneling rate constant of ferrocenylmethanol redox process on SAM was obtained from experimental results of scanning electrochemical microscopy. It is found that the electron tunneling across MPA SAM is faster than that of contrastive Methyl mercaptopropionate SAM. This result is attributed to the intermolecular interactions between the redox and MPA molecules. The conditions of lower pH and weaker ion pair effect all benefit the formation of the intermolecular interactions, resulting the enhancement of electron tunneling more obvious. Based on this, this kind of intermolecular interaction is inferred to be intermolecular hydrogen bond. Our work may have contributions to exploring electron tunneling between protein residues on biofilm surface.

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Reference:
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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Ferrocenylmethylation and alpha-ferrocenylethylation of indazole were carried out for the first time. Both reactions afforded two isomers, which were characterized by physical and physicochemical methods, among them by X-ray diffraction analysis. 1-(alpha-Ferrocenylethyl)indazole is thermally more stable than the 2-substituted isomer. Both isomers serve as ferrocenylalkylating agents with respect to s-triazole.

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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

 

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Conducting crystals of alternating ferrocene and diiodoacetylene units assembled into supramolecular 1-D chains via I?pi(Cp) halogen bonds were prepared and structurally characterized. Their structure and conductivity were compared with the ferrocene cocrystals with phenyliodoacetylene (C6H5C2I) and 1,4-di(ethynyliodo)phenylene. Electrical conductivity measurements of the ferrocene-based cocrystals revealed comparatively high electron-hole type conductivity in the ferrocene (FcH)-diiodoacetylene (C2I2) pair, a 3-order decrease in combination with the 1,4-di(ethynyliodo)phenylene linker, and it is virtually extinguished with the monotopic 1,2-phenyliodoacetylene. The increased electric conductivity of compound 1 is rationalized in terms of a weak charge transfer through the I?piCp halogen bonds in the [Cp-Fe-Cp?I-CC-I?]n polymeric chains.

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Reference:
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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Chemical engineers work across a number of sectors, processes differ within each of these areas, but chemistry and chemical engineering roles are found throughout, creation and manufacturing process of chemical products and materials. Application In Synthesis of 1,1′-Diacetylferrocene. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. Introducing a new discovery about 1273-94-5, Name is 1,1′-Diacetylferrocene

Poly(azine ferrocene-triazole-xanthone amide) (PAFTXA) was successfully synthesized from azine ferrocene bisacetylene (AFcB) and 2,7-(N-2-azidoacetamide) xanthone (NAzX) by using click chemistry protocol. In this paper, innovative AFcB moiety incorporated in this procedure as a monomer. This monomer was prepared in three steps from ferrocene scaffold, and the synthetic processes were discussed in details. Characterization of the synthesized novel intermediate materials, monomer, and the resulting polymer was performed by nuclear magnetic resonance, Fourier transform infrared, thermal gravimetric analysis, differential scanning calorimetry, and ultraviolet-visible spectrophotometer. In addition, the in vitro antibacterial activity of the polymer was appraised against Gram-positive and Gram-negative bacteria by using minimum inhibitory concentration method. Moreover; antitumoral effects of synthesized polymer were evaluated on Hela, MCF-7, and Saos cancer cell lines and compared with normal fibroblast cell line by means of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Promising antiproliferative effects were detected on both epitheloid and mesenchymal cancer cell lines depending on PAFTXA concentration and time. Survey on its characteristic features revealed the proficiencies of our prepared biomaterial such as its high thermal stability as well as valuable antitumoral and antibacterial capabilities that make it an appreciable candidate for further bioapplications.

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Reference:
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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n-BiVO4 is a promising semiconductor material for photoelectrochemical water oxidation. Although most thin-film syntheses yield discontinuous BiVO4 layers, back reduction of photo-oxidized products on the conductive substrate has never been considered as a possible energy loss mechanism in the material. We report that a 15 s electrodeposition of amorphous TiO2 (a-TiO2) on W:BiVO4/F:SnO2 blocks this undesired back reduction and dramatically improves the photoelectrochemical performance of the electrode. Water oxidation photocurrent increases by up to 5.5 times, and its onset potential shifts negatively by ?500 mV. In addition to blocking solution-mediated recombination at the substrate, the a-TiO2 film – which is found to lack any photocatalytic activity in itself – is hypothesized to react with surface defects and deactivate them toward surface recombination. The proposed treatment is simple and effective, and it may easily be extended to a wide variety of thin-film photoelectrodes.

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Reference:
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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A highly regioselective Ni-catalyzed hydroalkoxylation of 1,3-dienes is reported. The use of a (P,N) ligand is essential in achieving high levels of selectivity. The optimized protocol operates under particularly mild conditions, it provides access to a broad range of structurally diverse allylic ethers, and tolerates a number of sensitive functional groups.

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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

 

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A novel method for the preparation of magnetic porous carbon materials (MPMs) with high specific surfaces was developed using hydroxymethylferrocene through the combination of chloromethylation, hypercross-linked polymerization, and vacuum carbonization. The MPMs were mainly composed of porous carbon and iron nanoparticles. The specific surface and maximum specific saturation magnetization of MPMs were 295.90 m2/g and 7.45 emu/g, respectively. Furthermore, organic dyes, organic pesticides, and antibiotics were chosen as model adsorbates to test the adsorption properties of MPMs. The adsorption capacity of MPMs for methyl red was up to 199.54 mg/g at 120 min, and the adsorption isotherm was proved to fit the Langmuir isotherm model. The reuse results confirmed that MPMs had an excellent regenerative capacity and reusability stability. Moreover, MPMs showed superior removal efficiency for the rice field pesticides (emamectin benzoate, imidacloprid) and antibiotics (ampicillin). The above observations demonstrated that MPMs were universal to organic pollutants and would be one of the most promising candidates in the water purification filed.

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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

 

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Scanning electrochemical microscopy in feedback mode was used to monitor changes in the surface state of a polymeric film applied on a metallic substrate when exposed to an aqueous electrolytic environment. The protected metal consisted of a carbon steel substrate coated with a polyurethane-based polymeric film. SECM measurements performed in the presence and absence of chloride anions permitted a specific effect caused by Cl- anions at early exposures to be detected. Significant surface roughening is observed for immersion times shorter than 1 day when the electrolyte contains chloride ions. Additionally, the growth of an individual blister could also be investigated.

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Reference:
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