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The triethylenetetramine-functionalized graphene (TFGn) was prepared using graphene oxide (GO) and triethylenetetramine as raw materials through a one-step reaction under alkaline condition. The triethylenetetramine not only acted as cross-linker to combine GO, but also as reductant of GO. The TFGn was characterized by its ultraviolet spectrum (UV), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Raman spectroscopy and Scanning electron microscopy (SEM). The results showed that triethylenetetramine was successfully grafted onto the surface of the GO through covalent bonding between amine and epoxy groups. The resultant TFGn was uniformly dispersed in water over several weeks, suggesting that the introduction of amino groups greatly increased the hydrophilicity of TFGn. The triethylenetetramine-functionalized graphene was then applied to fabricate glucose biosensors with IO4- oxidized glucose oxidase (GOx) through layer-by-layer (LBL) self-assembly by the covalent bonding between the aldehyde groups of GOx and amino groups of TFGn. The gold electrodes modified with the (GOx/TFGn)n multilayer films were studied by cyclic voltammetry (CV) and showed outstanding electrocatalytical response to the oxidation of glucose when ferrocenemethanol was used as an artificial redox mediator. The response increased with an increasing number of GOx/TFGn bilayers, indicating that the analytical performance, such as the sensitivity of the glucose biosensor, could be adjusted by tuning the number of deposited GOx/TFGn bilayers. The linear response range of the biosensor constructed with six bilayers of GOx/TFGn to the concentration of glucose can extend to at least 8 mM with a sensitivity of 19.9 muA mM- 1 cm- 2. In addition, the sensor exhibited good stability due to the covalent interactions between the GOx and TFGn.

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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 ensure the efficiency and safety of chemical processes, adapt the chemical make-up of products to meet environmental or economic needs, and apply new technologies to improve existing processes. Safety of 1,1′-Dibromoferrocene. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. Introducing a new discovery about 1293-65-8, Name is 1,1′-Dibromoferrocene

A series of polysaccharide-based chiral stationary phase (CSP) columns, Daicel Chiralpak IA, IB, and IC, were applied in the separation of the nonenantiomeric isomers of various organometallic compounds and were found to be highly effective in recognizing isomers of minor structural differences. The CSP columns have succeeded to separate the double-bond regioisomers in bridged (eta5-formylcyclopentadienyl)manganese(I) dicarbonyl complexes 1a/1b, the structural isomers of methylbutenylferrocene derivatives in 2a/2b and 3a/3b, and the geometrical isomers of the (2-methyl-2-butenyl)ferrocenes in (Z)/(E)-3b. Due to the close similarity of the isomeric compounds in these mixtures, separations of the components are extremely difficult and could not be attained by conventional methods such as silica gel column chromatography, silica gel HPLC, recrystallization, distillation/sublimation, etc. Clearly, the polysaccharide-based CSP columns have unique advantages in separation/purification technology, and this study has shown potential usefulness of the CSP columns in separation of not only enantiomeric but also nonenantiomeric mixtures.

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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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Ferrocenoyl imidazolide is synthesized readily from ferrocenecarboxylic acid in one step. It is a red crystalline compound that is stable at <5C in the dark and it acts as an efficient ferrocenoyl equivalent. It reacts rapidly with alkoxides to give esters and with thiolates to give thioesters. Its reaction with Lawesson's reagent gave diferrocenoyl disulfide. Attempts to make diferrocenoyl peroxide by reacting ferrocenoyl imidazolide with hydrogen peroxide were unsuccessful. Ferrocenoyl imidazolide is converted into triferrocenylmethanol and diferrocenyl ketone in one step by reacting it with ferrocenyl-lithium. The X-ray crystal structures of ferrocenoyl phenyl sulfide and diferrocenoyl disulfide are described. Keep reading other articles of 1273-86-5! Don’t worry, you don’t need a PhD in chemistry to understand the explanations! Formula: C11H3FeO

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 procedure is outlined for fabricating well-behaved microelectrodes from ceramic pellets of YBa2Cu3O7 and Bi2Sr2CaCu2O8 which involves systematic polishing of an epoxy-encapsulated superconductor chip, under Et4NClO4/acetonitrile solution, to a potentiometric end point. Voltammetry of the resulting microelectrodes in acetonitrile is illustrated and compared to that arising from alternative superconductor electrode geometries. The microelectrodes have active electrode surface areas ranging from 2 × 10-6 to 3 × 10-4 cm2, as characterized electrochemically and microscopically. The results are significant steps toward developing the methodology necessary to study the electrochemical response of high temperature superconductor phases at temperatures below their superconductor critical temperature.

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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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Nitrogen-doped carbon nanotubes (N-CNTs) have been synthesized at 850 C via a CVD deposition technique by use of three ferrocenyl derivative catalysts, i.e. para-CN, -CF3 and -Cl substituted-phenyl rings. The synthesized catalysts have been characterized by NMR, IR, HR-MS and XRD. The XRD analysis of the para-CF3 catalyst indicates that steric factors influence the X-ray structure of 1,1?-ferrocenylphenyldiacrylonitriles. Acetonitrile or pyridine was used as carbon and nitrogen sources to yield mixtures of N-CNTs and carbon spheres (CS). The N-CNTs obtained from the para-CF3 catalysts, in pyridine, have the highest nitrogen-doping level, show a helical morphology and are less thermally stable compared with those synthesized by use of the para-CN and -Cl as catalyst. This suggests that fluorine heteroatoms enhance nitrogen-doping in N-CNTs and formation of helical-N-CNTs (H-N-CNTs). The para-CF3 and para-Cl catalysts in acetonitrile yielded iron-filled N-CNTs, indicating that halogens promote encapsulation of iron into the cavity of N-CNT. The use of acetonitrile, as carbon and nitrogen source, with the para-CN and -Cl as catalysts also yielded a mixture of N-CNTs and carbon nanofibres (CNFs), with less abundance of CNFs in the products obtained using para-Cl catalysts. However, para-CF3 catalyst in acetonitrile gave N-CNTs as the only shaped carbon nanomaterials.

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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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Condensation of aromatic, isoxazole, and ferrocene aldehydes as well as 1,1?-diacetylferrocene with 5-(4-methylphenyl)isoxazole-3-carbohydrazonamide afforded various N-substituted azines with molecular fragments of the corresponding aldehydes or diacetylferrocene.

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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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Iron oxide nanoparticles have attracted a great deal of research interest and have been widely used in bioscience and clinical research including as contrast agents for magnetic resonance imaging, hyperthermia and magnetic field assisted radionuclide therapy. It is therefore important to develop methods, which can provide high-throughput screening of biological responses that can predict toxicity. The use of nanoelectrodes for single cell analysis can play a vital role in this process by providing relatively fast, comprehensive, and cost-effective assessment of cellular responses. We have developed a new method for in vitro study of the toxicity of magnetic nanoparticles (NP) based on the measurement of intracellular reactive oxygen species (ROS) by a novel nanoelectrode. Previous studies have suggested that ROS generation is frequently observed with NP toxicity. We have developed a stable probe for measuring intracellular ROS using platinized carbon nanoelectrodes with a cavity on the tip integrated into a micromanipulator on an upright microscope. Our results show a significant difference for intracellular levels of ROS measured in HEK293 and LNCaP cancer cells before and after exposure to 10 nm size iron oxide NP. These results are markedly different from ROS measured after cell incubation with the same concentration of NP using standard methods where no differences have been detected. In summary we have developed a label-free method for assessing nanoparticle toxicity using the rapid (less than 30 minutes) measurement of ROS with a novel nanoelectrode.

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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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Probing a switch on biomimic membrane surfaces would offer some references to the research on permeability of cytomembranes. In this work, a mixed 11-mercaptoundecanoic acid/1-undecanethiol self-assembled monolayer (MUA/UT SAM) was constructed as a model of a biomembrane. In this mixed SAM, the MUA molecules work as functional parts for the switch and the UT molecules work as diluents. The surface coverage, wetting property, and pKa of this mixed SAM all have been well-inspected. The mixed SAM exhibits excellent switchable properties for cations, which is well-monitored by scanning electrochemical microscopy. When the pH of a solution is higher than the pKa, protons would stimulate a shift of dissociation equilibrium of terminal carboxyl groups. The dissociated carboxylate ions would lead to a switch on the state of the SAM. Otherwise, the SAM shows an off state when the pH is lower than the pKa. In addition, the repeatability, applicability, and the mechanism of the switch all have been well-evaluated.

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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 preparation and characterization of the three ferrocene based dithiolane complexes [(eta5-C5H5) Fe(eta5-C5H4)NHC(O)(CH2)4CHS 2CH2CH2]1, [(eta5- C5H5)Fe(eta5-C5H 4)CH2OC(O)(CH2)4CHS2CH 2CH2] 2 and [(eta5-C5H 5)Fe(eta5-C5H4)NHC(O)(CH 2)CHS2CH2CH2] 3, with different spacer groups between the ferrocenyl moiety and the dithiolane unit, are reported. The complexation of 1 and 2, using the oxidative addition of the S-S bonds to Pt(0), is also described, leading to the square planar Pt(II) complexes [Pt(PPh3)2(S2CH2CH 2CH-kappa2-S,S)(CH2)4C(O) NH(eta5-C5H4)Fe(eta5-C 5H5)] 4 and [Pt(PPh3)2(S 2CH2CH2CH-kappa2-S,S)(CH 2)4C(O)OCH2(eta5-C 5H4)Fe(eta5-C5H5)] 5, respectively. The reduction of the S-S bond in 1 and 2 yields the corresponding dithiols; these can be deprotonated and treated with ClSiMe3 to prepare [(eta5-C5H5)Fe(eta5- C5H4)NHC(O)(CH2)4CH(SSiMe 3)CH2CH2(SSiMe3)] 7 and [(eta5-C5H5)Fe(eta5-C 5H4)CH2OC(O)(CH2) 4CH(SSiMe3)CH2CH2(SSiMe 3)] 9, respectively. The complexes were characterized via NMR and UV-Vis absorption spectroscopy, cyclic voltammetry and single crystal X-ray diffraction for 1 and 4.

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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. Formula: C11H3FeO. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. Introducing a new discovery about 1273-86-5, Name is Ferrocenemethanol

Cobalt(II) complexes (5 mol% Co) bearing phosphine-free N?N?N pincer ligands efficiently catalyze C?C coupling of secondary and primary alcohols to selectively form alpha-alkylated ketones with a good functional group compatibility using NaOH (20 mol%) as a base at 120 C. The NH group on the N?N?N?Co(II) precatalyst controls the activity and selectivity. This simple catalytic system is involved in the synthesis of quinolones via the dehydrogenative annulation of 2-aminobenzyl alcohols with secondary alcohols.

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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