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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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Acetyl ferrocene and diacetyl ferrocene both readily react with an excess of hydrazine to afford the corresponding hydrazone compounds. These compounds can then be linked to Re(CO)3 via a metal-mediated Schiff base reaction, resulting in a series of ferrocene-Re(CO)3 conjugates with different stoichiometries. Conjugates with 1:1, 1:2, and 2:1 ferrocene: Re(CO)3 ratios can be produced via this “modular” type synthesis approach. Several examples of these conjugates were structurally characterized, and their spectroscopic, electrochemical, and spectroelectrochemical behaviors were investigated. The electronic structures of these compounds were also probed using DFT and TDDFT calculations.

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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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Diabetes is a group of heterogeneous disorders with the common elements of hyperglycemia and glucose intolerance because of insulin deficiency, impaired effectiveness of insulin action or both. The best marker for long-term glycemic control is whole-blood glycated hemoglobin (HbA1c), since its levels correspond to the long-term progression of diabetes without short-term fluctuations in the behavior of glucose. Currently, common laboratory methods to recognize glycated proteins are high-performance liquid chromatography, immunoassay and electrophoresis. The accuracy and the precision of A1C assays at least match those of glucose assays. Consequently, the International Expert Committee (with members appointed by the American Diabetes Association, the European Association for the Study of Diabetes, and the International Diabetes Federation) decided that the A1c assay should be recognized as the primary method for diagnosing diabetes. In this review, we look at electrochemical biosensors for the detection of glycated proteins developed in recent years.

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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 […] of highly dilute preparation method, comprises the following steps: step 1), in the added into the dry CH […] in2 Cl2 , Pyridine and aniline derivatives stirring after; step 2), non-water treated CH2Cl2 dissolved 1, 1′ – ferrocene dicarboxylic acyl chloride, to slowly dropping in the […], after dropping the first reaction is carried out at room temperature, then slow heating, reflux; monitoring the reaction process for thin plate and, when one of the raw material point disappears, stopping the reaction; step 3), evaporate solution in dichloromethane, residual liquid water washing several times, the collected organic phase with anhydrous MgSO4 After drying the solvent evaporate under reduced pressure, then to admix the residual liquid in the silica gel, eluting agent selected: VPetroleum ether : VAcetic acid ethyl ester =3:1 elution, column purification, to obtain a final […]. The invention can simplify the link flourishing synthetic process, improve its productive rate with the fluorescence intensity, save the process cost. (by machine translation)

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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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Ferrocenyltrithiocarbonates (I) are readily obtained by treating alpha-ferrocenylcarbinols (II) successively with sodium hydride, carbon disulfide and alkyl halide.Formation of I occurs by intramolecular nucleophilic displacement of oxygen by sulfur with retention of configuration.This is supported by the nature of the other products formed and by the X-ray structure determination of an optically active compound I, which was refined to R = 0.038.The title compound of R configuration was obtained from (R)-ferrocenylmethylmethanol.

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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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Biomolecules are integral constituents of living beings which regulate numerous biochemical functions of the body. Analysis of various small molecules (metabolites, neurotransmitters, amino acids, vitamins) and macromolecules (nucleic acids, proteins) is of prime importance in modern time due to increasing disbalance in natural metabolism of human body. Irregularities and alteration in concentration of biomolecules lead to different kinds of genetic, metabolic and cancerous diseases which have created a great requirement of highly sensitive, accurate and stable detection systems for their quick and specific screening. In this review, redox interactions of biomolecules at carbon based electrode interfaces have been discussed using voltammetry. It is divided into subsections, starting with an introduction into the field and a description of its current state. This is followed by a large section describing carbon nanomaterials (CNs) based voltammetric sensors for different small biomolecules and macromolecules. The next section of the review gives conclusion, challenges and future perspectives in sensing biomolecules at CNs based electrodes. Advanced approaches for fabrication of portable integrated electrochemical devices for various point of care diagnostic applications have also been included at the end.

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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 micro supported lipid bilayer (SLB) electrophoresis method was developed, which functions at low potentials and appreciable operating times. To this end, (hydroxymethyl)-ferrocene (FcCH2OH) was employed to provide an electrochemical reaction at the anode and cathode at low applied potential to avoid electrolysis of water. The addition of FcCH2OH did not alter the SLB characteristics or affect biomolecule function, and pH and temperature variations and bubble formation were eliminated. Applying potentials of 0.25-1.2 V during flow gave homogeneous electrical fields and a fast, reversible, and strong build-up of a charged dye-modified lipid in the direction of the oppositely charged electrode. Moreover, streptavidin mobility could be modulated. This method paves the way for further development of analytical devices.

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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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One problem encountered in the development of rechargeable lithium batteries is protection of individual cells from overcharging. In this work the addition of metallocene derivatives to cell electrolytes to provide overcharge protection was investigated. Eleven ferrocene derivatives were studied in terms of their redox potentials and mass transport properties in electrochemical cells and ‘AA’ size Li/LixMnO2 rechargeable cells employing 1M LiAsF6 in 50/50 volume percent propylene carbonate/ethylene carbonate (PC/EC) as the electrolyte. The chemical and electrochemical properties of these metallocene derivatives were also studied in terms of the chemical stability of the derivatives toward cell components and electrochemical reversibility in long-term cycling studies. It was found that adsorption of one derivative, dimethylaminomethylferrocene, on the LixMnO2 electrode (DeltaGads = -3.8 Kcal mol-1 based on the Langmuir adsorption isotherm), blocked the intercalation of Li+ ions into the LixMnO2 electrode.

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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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The electrolytes used in enzymatic biosensors or biofuel cells have always been considered to be inert. However, recent studies have demonstrated that this assumption is not correct and that the nature of the electrolyte needs to be considered. Ion-specific interactions can occur with the faradaic response observed in both direct and mediated electron transfer being modulated by the nature of the salt used in solution. Specific ion effects arise from the Hofmeister series, which is well established in studies of protein systems but not in electrochemical studies of redox enzymes. Recent experimental and theoretical work on explaining the Hofmeister effect is described.

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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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<3.3>(1,1′)Ruthenocenophane-2,14-diene-1,16-dione, <5.5>(1,1′)ruthenocenophane-2,14,17,29-tetraene-1,16-dione and their ferrocenoruthenocenophane homologs were synthesized by using an intramolecular base-catalyzed condensation.

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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