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Enantiopure Ferrocene-Based Planar-Chiral Iridacycles: Stereospecific Control of Iridium-Centred Chirality

Reaction of [IrCp?Cl2]2 with ferrocenylimines (Fc=NAr, Ar=Ph, p-MeOC6H4) results in ferrocene C-H activation and the diastereoselective synthesis of half-sandwich iridacycles of relative configuration Sp?,RIr?. Extension to (S)-2-ferrocenyl-4-(1-methylethyl)oxazoline gave highly diastereoselective control over the new elements of planar chirality and metal-based pseudo-tetrahedral chirality, to give both neutral and cationic half-sandwich iridacycles of absolute configuration Sc,Sp,RIr. Substitution reactions proceed with retention of configuration, with the planar chirality controlling the metal-centred chirality through an iron-iridium interaction in the coordinatively unsaturated cationic intermediate.

Enantiopure Ferrocene-Based Planar-Chiral Iridacycles: Stereospecific Control of Iridium-Centred Chirality

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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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Pyrrolidinyl PNA polypyrrole/silver nanofoam electrode as a novel label-free electrochemical miRNA-21 biosensor

A label-free electrochemical miRNA biosensor was developed based on a pyrrolidinyl peptide nucleic acid (acpcPNA)/polypyrrole (PPy)/silver nanofoam (AgNF) modified electrode. The AgNF was electrodeposited as redox indicator on a gold electrode, which was then functionalized with an electropolymerized layer of PPy, a conducting polymer, to immobilize the PNA probes. The fabrication process was investigated by electrochemical impedance spectroscopy. The biosensor was used to detect miRNA-21, a biomarker abnormally expressed in most cancers. The signal was monitored by the change in current of the AgNF redox reaction before and after hybridization using cyclic voltammetry. Two PNA probe lengths were investigated and the longer probe exhibited a better performance. Nucleotide overhangs on the electrode side affected the signal more than overhangs on the solution side due to the greater insulation of the sensing surface. Under optimal conditions, the electrochemical signal was proportional to miRNA-21 concentrations between 0.20 fM and 1.0 nM, with a very low detection limit of 0.20 fM. The biosensor showed a high specificity which could discriminate between complementary, single-, doubled-base mismatched, and non-complementary targets. Three out of the seven tested plasma samples provided detectable concentrations (63 ¡À 4, 111 ¡À 4 and 164 ¡À 7 fM). The sensor also showed good recoveries (81?119%). The results indicated the possibilities of this biosensor for analysis without RNA extraction and/or amplification, making the sensor potentially useful for both the prognosis and diagnosis of cancer in clinical application.

Pyrrolidinyl PNA polypyrrole/silver nanofoam electrode as a novel label-free electrochemical miRNA-21 biosensor

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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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Electric Literature of 1273-86-5, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 1273-86-5, molcular formula is C11H3FeO, introducing its new discovery.

Argon plasma treatment to enhance the electrochemical reactivity of screen-printed carbon surfaces

Radiofrequency argon plasma was used for screen-printed carbon electrodes (SPCE) surface treatment. The cyclic voltammetry of ferri/ferrocyanide as redox couple showed a remarkable improvement of the electrochemical reactivity of the SPCE after the plasma treatment. The effect of the plasma growth conditions on the efficiency of the treatment procedure was evaluated in term of electrochemical reactivity of the SPCE surface. The electrochemical study showed that the electrochemical reactivity of the treated electrodes was strongly dependant on radiofrequency power, treatment time and argon gas pressure. X-ray photoelectron spectroscopy (XPS) analysis showed a considerable evolution on the surface chemistry of the treated electrodes. Our results clearly showed that the argon plasma treatment induces a significant increase in the Csp2/Csp3 ratio. The scanning electron micrograph (SEM) also showed a drastic change on the surface morphology of the treated SPCEs.

Argon plasma treatment to enhance the electrochemical reactivity of screen-printed carbon surfaces

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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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The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2012

This is a review of papers published in the year 2012 that focus on the synthesis, reactivity, or properties of compounds containing a carbon-transition metal double or triple bond.

The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2012

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 1273-86-5, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1273-86-5, in my other articles.

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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The enhanced electronic communication in ferrocenemethanol molecular cluster based on intermolecular hydrogen-bonding

This work presents an electrochemical study of enhanced electronic communication based on intermolecular hydrogen-bonding in ferrocenemethanol (described as FcCH2OH) molecular clusters. The enhanced electronic communication in FcCH2OH clusters is confirmed and further investigated by differential-pulse voltammetry and cyclic voltammetry. A key finding is that this enhanced electronic communication increases the standard rate constant of the electron transfer process. These results will provide us with a further understanding of the electronic communication within the ferrocenyl derivatives which is based on the intermolecular hydrogen-bonding.

The enhanced electronic communication in ferrocenemethanol molecular cluster based on intermolecular hydrogen-bonding

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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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Regulating the intermolecular hydrogen bonding: The reversible assembly and disassembly in the diffusion layer

The intermolecular hydrogen bonding between 3-mercaptopropionic acid (MPA) and ferrocenylmethanol (FcCH2OH) on the tip electrode was studied by scanning electrochemical microscopy (SECM). The reversible assembly and disassembly of the intermolecular hydrogen bonding were designed with the aid of the dissociation equilibrium of the terminal carboxyl groups (-COOH) of the MPA self-assembled monolayer (SAM). Based on this design, the pH-modulated assembly and disassembly of intermolecular hydrogen bonding have been implemented. The use of well-defined SAM as model membrane provides a simple yet practicable approach to explore the molecular recognition at the cell membrane surfaces.

Regulating the intermolecular hydrogen bonding: The reversible assembly and disassembly in the diffusion layer

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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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Amphiphilic bimetallic polymer as single-source precursors for the one-pot synthesis of L10-phase FePt nanoparticles

Amphiphilic polymers have attracted extensive research attention in constructing various nanostructures by self-assembly. Here we designed and synthesized two amphiphilic bimetallic polymers with different length of the tails P1 and P2, in which Fe,Pt-containing conjugated complex acted as the hydrophobic block and hydrophilic poly(ethylene glycol)(PEG)was bonded to the bimetallic core as the flexible tails. P1 and P2 were used as the single-source precursors to prepare FePt nanoparticles (NPs)by one-pot pyrolysis. The resultant NPs were fully characterized and had a chemically ordered face-centered tetragonal (fct)phase with high crystallinity. The size of NPs pyrolyzed from P1 and P2 was 24.7 and 8.2 nm with the relative coercivity of 9.6 and 1.3 kOe, respectively. The difference was preliminarily explained by the discrepancy of their degrees of crystallinity, and also analyzed by the precursors? structural effect. The amphiphilic design showed a good potential in preparing monodisperse ferromagnetic FePt NPs, and the possible favorable properties of self-assembly might provide a bright venue for future magnetic recording media.

Amphiphilic bimetallic polymer as single-source precursors for the one-pot synthesis of L10-phase FePt nanoparticles

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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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Role of the Carbon Support on the Oxygen Reduction and Evolution Activities in LaNiO3 Composite Electrodes in Alkaline Solution

Metal-air batteries and fuel cells show a great deal of promise in advancing low-cost, high-energy-density charge storage solutions for sustainable energy applications. To improve the activities and stabilities of electrocatalysts for the critical oxygen reduction and evolution reactions (ORR and OER, respectively), a greater understanding is needed of the catalyst/carbon interactions and carbon stability. Herein, we report how LaNiO3 (LNO) supported on nitrogen-doped carbon nanotubes (N-CNT) made from a high-yield synthesis lowers the overpotential for both the OER and ORR markedly to enable a low bifunctional window of 0.81 V at only a 51 mug cm-2 mass loading. Furthermore, the addition of LNO to the N-CNTs improves the galvanostatic stability for the OER by almost 2 orders of magnitude. The nanoscale geometries of the perovskites and the CNTs enhance the number of metal-support and charge transfer interactions and thus the activity. We use rotating ring disk electrodes (RRDEs) combined with Tafel slope analysis and ICP-OES to quantitatively separate current contributions from the OER, carbon oxidation, and even anodic iron leaching from carbon nanotubes.

Role of the Carbon Support on the Oxygen Reduction and Evolution Activities in LaNiO3 Composite Electrodes in Alkaline Solution

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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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Sensitive chemically amplified electrochemical detection of ruthenium tris-(2,2?-bipyridine) on tin-doped indium oxide electrode

Optimized combination of chemical agents was selected for sensitive electrochemical detection of dissolved ruthenium tris-(2,2?-bipyridine) (Ru-bipy). The detection was based on the chemical amplification mechanism, in which the anodic current of a redox-active analyte was amplified by a sacrificial electron donor in solution. On indium-doped tin oxide (ITO) electrodes, electrochemical reaction of the analyte was reversible, but that of the electron donor was greatly suppressed. Several transition metal complexes, such as ferrocene and tris-(2,2?-bipyridine) complexes of osmium, iron and ruthenium, were evaluated as model analyte. A correlation between the amplified current and the standard potential of the complex was observed, and Ru-bipy generated the largest current. A variety of organic bases, acids and zwitterions were assessed as potential electron donor. Sodium oxalate was found to produce the largest amplification factor. With Ru-bipy as the model analyte and oxalate as the electron donor, the analyte concentration curve was linear up to 50muM, with a lower detection limit of approximately 50nM. Preliminary work was presented in which a Ru-bipy derivative was attached to bovine serum albumin and detected electrochemically. Although the combination of Ru-bipy, oxalate and ITO electrode has been used before for electrochemiluminescent detection of Ru-bipy and oxalate, as well as electrochemical detection of oxalate, its utility in amplified voltammetric detection of Ru-bipy as a potential electrochemical label has not been reported previously.

Sensitive chemically amplified electrochemical detection of ruthenium tris-(2,2?-bipyridine) on tin-doped indium oxide electrode

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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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FERROCENDERIVATE. LXV. 57Fe-KERNRESONANZSPEKTROSKOPIE VON FERROCENDERIVATEN

57Fe NMR spectra of 20 ferrocene derivatives with natural abundance of 57Fe have been recorded by the conventional pulse Fourier transform technique using ferrocene as internal standard for the chemical shifts.Shift contributions of the substituents are discussed qualitatively.

FERROCENDERIVATE. LXV. 57Fe-KERNRESONANZSPEKTROSKOPIE VON FERROCENDERIVATEN

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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