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Electrically transmissive alkyne-anchored monolayers on gold

Well-ordered, tightly-packed (surface coverage 0.97 ¡Á 10-9 mol cm-2) monolayer films of 1,4-bis((4-ethynylphenyl)ethynyl)benzene (1) on gold are prepared via a simple self-assembly process, taking advantage of the ready formation of alkynyl C-Au sigma-bonds. Electrochemical measurements using [Ru(NH3)6]3+, [Fe(CN)6]3-, and ferrocenylmethanol [Fe(eta5-C5H4CH2OH)(eta5-C5H5)] redox probes indicate that the alkynyl C-Au contacted monolayer of 1 presents a relatively low barrier for electron transfer. This contrasts with monolayer films on gold of other oligo(phenylene ethynylene) derivatives of comparable length and surface coverage, but with different contacting groups. Additionally, a low voltage transition (Vtrans = 0.51 V) from direct tunneling (rectangular barrier) to field emission (triangular barrier) is observed. This low transition voltage points to a low tunneling barrier, which is consistent with the facile electron transport observed through the C-Au contacted self-assembled monolayer of 1.

Electrically transmissive alkyne-anchored monolayers on gold

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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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Benzoquinone modified electrode for sensing NADH and ascorbic acid

A benzoquinone modified basal plane pyrolytic graphite electrode shows electrocatalytic activity for the oxidation of NADH and ascorbic acid in phosphate buffer (pH 7.3). The modified electrode shows a linear variation of catalytic current with concentration in the range 1-10 mM for both NADH and ascorbic acid. The rate constants have been estimated from the surface coverage data.

Benzoquinone modified electrode for sensing NADH and ascorbic acid

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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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Emerging pnictogen-based 2D semiconductors: Sensing and electronic devices

Pnictogens are an intensively studied group of monoelemental two-dimensional materials. This group of elements consists of phosphorus, arsenic, antimony, and bismuth. In this group, the elements adopt two different layered structural allotropes, orthorhombic structure with true van der Waals layered interactions and rhombohedral structure, where covalent interactions between layers are also present. The orthorhombic structure is well known for phosphorus and arsenic, and the rhombohedral structure is the most thermodynamically stable allotropic modification of arsenic, antimony, and bismuth. Due to the electronic structure of pnictogen layers and their semiconducting character, these materials have huge application potential for electronic devices such as transistors and sensors including photosensitive devices as well as gas and electrochemical sensors. While photodetection and gas sensing applications are often related to lithography processed materials, chemical sensing proceeds in a liquid environment (either aqueous or non-aqueous) and can be influenced by surface oxidation of these materials. In this review, we explore the current state of pnictogen applications in sensing and electronic devices including transistors, photodetectors, gas sensors, and chemical/electrochemical sensors.

Emerging pnictogen-based 2D semiconductors: Sensing and electronic devices

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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 ferrocene-containing group of the carbamate compound and its synthesis method (by machine translation)

The invention discloses a carbamate compounds containing ferrocene group and its synthesis method, which belongs to the field of high molecular. The invention also discloses a containing ferrocene group of the carbamate compound preparation method. The invention containing ferrocene group a carbamate compound, chemical quality good stability, has a plurality of catalytic characteristics; for lubricating oil additive, at the same time has good oxidation resistance, abrasion resistance and corrosion resistance; for fuel oil additive, with smoke combustion-supporting, the advantages of reducing pollution. (by machine translation)

A ferrocene-containing group of the carbamate compound and its synthesis method (by machine translation)

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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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Synthesis of versatile intermediates of the ferrocene series: Reductive amination of ferrocenecarbaldehyde

Reductive amination of ferrocenecarbaldehyde with several primary and secondary amines in the presence of sodium triacetoxyborohydride was studied. This method was used for the synthesis of new ferrocenylmethylamines, viz., N-(ferrocenylmethyl)isoleucine methyl ester, N,N-bis(ferrocenylmethyl)glycine ethyl ester, and N-(3,5-dibenzyloxybenzyl)-N-(ferrocenylmethyl)methylamine. The latter is a potential precursor of a dendrimer with the chiral ferrocenyl plane in the core.

Synthesis of versatile intermediates of the ferrocene series: Reductive amination of ferrocenecarbaldehyde

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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

 

Discovery of Ferrocenemethanol

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Electrochemistry of ferrocenylphosphines FcCH2PR2 (Fc=(eta5-C5H5)Fe(eta5- C5H4); R=Ph, CH2OH and CH2 CH2CN), and some phosphine oxide, phosphine sulfide, phosphonium and metal complex derivatives

Electrochemical studies of the free ferrocenylphosphine ligands FcCH2PR2 (Fc=(eta5-C5 H5)Fe(eta5-C5H4); R=Ph, CH2OH and CH2CH2CN) and some phosphine oxide, phosphine sulfide, phosphonium and metal derivatives are described. The free ligands exhibit complex voltammetric responses due to participation of the phosphorus lone pair in the redox reactions. Uncomplicated ferrocene-based redox chemistry is observed for PV derivatives and when the ligands are coordinated in complexes cis-PtCl2[FcCH2P(CH2OH) 2], PdCl2[FcCH2P(CH2OH) 2], [Au{FcCH2P(CH2OH)2} 2]Cl, RuCl2(eta6-C10 H14)[FcCH2P(CH2OH)2] and RuCl2(eta6-C10H14) (FcCH2PPh2). The reaction pathways of the free ligands after one-electron oxidation have been examined in detail using voltammetry, NMR spectroscopy and electrospray mass spectrometry. Direct evidence for formation of a P-P bonded product is presented.

Electrochemistry of ferrocenylphosphines FcCH2PR2 (Fc=(eta5-C5H5)Fe(eta5- C5H4); R=Ph, CH2OH and CH2 CH2CN), and some phosphine oxide, phosphine sulfide, phosphonium and metal complex derivatives

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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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Ylide Complexes of Alkali and Earth Alkaline Metals, VI. Neutral and Anionic Ferrocenylmethylides and Fluorenylides

Coordination properties of phosphorus ylides towards electropositive metals are greatly improved in systems, where the carbanionic charge can be delocalized into the aromatic rings of substituents, as illustrated in the title compounds.The ferrocenyl-substituted ylide 2, synthesized from bis(diphenylphosphino)methane and (ferrocenyl)trimethylammonium iodide via the phosphonium salt intermediate 1, is thus easily converted into the alkali complexes 3a, b on treatment with NaNH2 or KH in tetrahydrofuran, respectively.The intensely coloured products are soluble in a number of organic solvents.NMR spectra of these solutions provide evidence for an interaction between alkali cations and the ferrocenyl rings. – From (C6H5)2CH2P(C6H5)2 and ferrocenylmethyl chloride a diquaternary salt 4 is obtained, which yields a double-ylide mixture 5a, b on treatment with base.Hydrolysis of this product affords the ylidic phosphine oxide 6. – The reaction of the ylides 7 and 9 (described previously) with NaNH2, KH or barium metal (in liquid ammonia) leads to the (earth) alkali complexes 8a-c and 10a, b, respectively.With the exception of 8c, but similar to 3a, these materials contain tetrahydrofuran solvate molecules.The 23Na NMR spectrum of 8a and the pronounced quadrupole broadening of the P(III) signals by the alkali cations in the 31P NMR spectra of 8a, b allow structural suggestions for the solution state as proposed in the formulae.Further treatment of 10b with KH yields a potassium complex 11, characterized, i.a., via a corresponding diquaternary salt 12. – Keywords: Ylides, Alkali Complexes, Phosphonium Salts, Phosphonium Ferrocenylmethylides

Ylide Complexes of Alkali and Earth Alkaline Metals, VI. Neutral and Anionic Ferrocenylmethylides and Fluorenylides

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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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Reagentless recycling of pyruvate oxidase on a conducting polymer-modified electrode

The enzyme pyruvate oxidase (PyOD) covalently immobilized on an original conducting copolymer poly(5-hydroxy-1,4-naphthoquinone-co-5-hydroxy-3-thioacetic-1,4-naphthoq uinone acid) can be recycled under anaerobic conditions, at +0.1 V versus SCE. It is first demonstrated that the quinone group is an efficient co-substrate for PyOD in homogeneous conditions, then this efficiency is preserved when the quinone group is embedded in the polymer structure. The copolymer remains efficient even in aerated media. The low working potential avoids side-oxidations of interfering species as ascorbic acid or salycilate.

Reagentless recycling of pyruvate oxidase on a conducting polymer-modified 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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Novel method for rapid toxicity screening of magnetic nanoparticles

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.

Novel method for rapid toxicity screening of magnetic 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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A synthesis method of alpha- the alkyl is fragrant acetamide (by machine translation)

The present invention discloses a synthetic alpha- the alkyl is fragrant acetamide method. In the reaction container, adding fragrant second grade nitrile, the compound is mellow, a transition metal catalyst complex of metal, alkali, and an organic solvent to the metallisation; or the microwave reactor the reaction mixture under stirring with magnetic force, 130 C after the reaction, cooling to room temperature, then through the column separation, to obtain a target compound. From nitrile and mellow of the present invention as a starting material, in the transition metal catalyst, with the participation of the metallisation and alkali, direct synthesis of alpha-alkyl benzene acetamide, reaction exhibit three significant advantages: 1) the use of commercial or easily prepared nitrile and almost non-toxic alcohol as the starting material; 2) reaction atom economy is high; therefore, the reaction in accordance with the requirement of green chemistry, has broad prospects of development. (by machine translation)

A synthesis method of alpha- the alkyl is fragrant acetamide (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