5,141 research outputs found

    Aryl diazonium modification on graphite electrode in microbial fuel cell: a review

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    Usage of graphite electrode in a microbial fuel cell (MFC) is favored due to their electron conductivity and stability as a base material for the electrode. Also, graphite is favored as it allows the growth of biofilm, which can enhance the cell’s performance. The efficiency is reported improved through modification. Aryl diazonium modification has been reported to induce biofilm formation on the electrode faster. The modification can be done spontaneously or through electrografting of aryl diazonium salt onto the electrode surface. Control over the quantity of grafted aryl diazonium is essential. A thick layer will cause the performance of the system to drop, which may impede the electron transfer from biofilm to the electrode. Aryl diazonium is preferred as it allows a robust biofilm formation when used as a surface modification on the graphite electrode. Modification using aryl diazonium allows the electrode to be more accommodative for biofilm growth, which will increase the performance of the system. However, it does not act as a redox mediator for the system. It has been reported that power density obtained using aryl diazonium modified electrode is 250 mW.m-2, higher than unmodified graphite electrode of 125 mW.m-2. However, not all bacterial species is compatible with aryl diazonium modification. The unmodified graphite biocathode allows a higher power density compared to aryl diazonium modified biocathode. Hence, depending on the quality of aryl diazonium modification and the types of inoculum used, MFC performance can be further maximized

    One-pot radioiodination of aryl amines via stable diazonium salts: preparation of 125I-imaging agents

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    An operationally simple, one-pot, two-step tandem procedure that allows the incorporation of radioactive iodine into aryl amines via stable diazonium salts is described. The mild conditions are tolerant of various functional groups and substitution patterns, allowing late-stage, rapid access to a wide range of 125I-labelled aryl compounds and SPECT radiotracers

    A dual catalytic strategy for carbon-phosphorus cross-coupling via gold and photoredox catalysis.

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    A new method for the P-arylation of aryldiazonium salts with H-phosphonates via dual gold and photoredox catalysis is described. The reaction proceeds smoothly at room temperature in the absence of base and/or additives, and offers an efficient approach to arylphosphonates. The reaction is proposed to proceed through a photoredox-promoted generation of an electrophilic arylgold(III) intermediate that undergoes coupling with the H-phosphonate nucleophile

    A versatile route to modify polyethersulfone membranes by chemical reduction of aryldiazonium salts

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    International audienceUltrafiltration polyethersulfone membranes were modified covalently by chemical reduction of aryl diazonium salts. Functionalizations were performed with four aryl diazonium salts bearing different functional groups (4-benzyltriphenylphosphonium diazonium, 4-nitrophenyl diazonium, 4-benzonitrile diazonium and 4-phenylacetic acid diazonium) so as to demonstrate the versatility of the method. The efficiency of the different functionalizations was checked with various characterization techniques. Attenuated Total Reflectance Fourier Transform Infra Red spectroscopy revealed the presence of 4-nitrophenyl, 4-benzonitrile and 4-phenylacetic acid groups at the surface of the different modified membranes but no characteristic vibration band was detected on the surface of the membrane modified with 4-benzyltriphenylphosphonium diazonium. The presence of 4-benzyltriphenylphosphonium, however, could be demonstrated by both Energy Dispersive X-ray spectroscopy (detection of the Kα ray of phosphorous at 2.015 keV) and streaming current measurements (shift of the membrane isoelectric point). Finally, dead-end filtration of an antibiotic (tylosin) was carried out with the unmodified membrane and the membrane modified by 4-benzyltriphenyl-phosphonium diazonium. Experiments revealed that the transport properties of the grafted membrane were significantly modified, with a significant increase in rejection mainly due to electrostatic repulsions between the surface of the modified membrane and tylosin

    Indirect Electrografting of Aryl Iodides

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    International audienceThe electrografting of 4-iodonitrobenzene that is not possible directly is demonstrated whilst that of 5-iodo-2-amino-pyridine, 4-iodoaniline and iodobenzene is performed with a decrease of overpotential > 2 V. The electrografting of aryl iodides is achieved through a iodine abstraction reaction: in the presence of a sterically hindered diazonium salt (2,6-dimethylbenzenediazonium), the aryl iodide is grafted to gold at the much less negative reduction potential of the diazonium salt

    Covalent Bonding of Organic Molecules to Cu and Al Alloy 2024 T3 Surfaces via Diazonium Ion Reduction

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    Cu surfaces and polished aluminum alloy 2024 T3 substrates were derivatized at open-circuit potential with aryl diazonium salts in both aprotic and aqueous media. Raman spectroscopy confirmed the presence of a derivatized film on the substrates before and after exposure to boiling water and sonication in acetone. Two different Cu substrate surfaces were prepared and used for X-ray photoelectron spectroscopy (XPS) analysis of the derivatization results. One surface was native oxide Cu, predominantly in the form of Cu_2O, and one surface was predominantly Cu^0. Results of the XPS analysis indicate the presence of both a Cu-O-C linkage and a Cu-C covalent bond between the aryl ring and the Cu substrate, and a high coverage of the organic layer. XPS results also indicate the formation multilayers on both types of Cu surfaces with different percentages of azo coupling within the multilayers on the two surfaces. Applications of a covalently bonded organic film on copper and alloy surfaces include adhesion promotion, corrosion protection, and possibly inhibition of oxygen reduction

    On the chemical grafting of titanium nitride by diazonium chemistry †

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    International audienceCurrent research directions with the aim of extending the applications of titanium nitride (TiN) in areas of microelectronics, electrocatalysis, biosensors etc. require identifying new and efficient methods to modify this durable material with desired organic functionalities. We have clearly demonstrated in this work that diazonium chemistry can be considered for surface modification of titanium nitride. Indeed, a near-monolayer of aminophenylene has been reported to be spontaneously grafted onto the TiN surface by simple immersion of the substrates into an acidic solution of the corresponding diazonium cations. X-ray photoelectron spectroscopy measurements strongly suggested a covalent coating of aminophenyl groups on titanium nitride. Surface functionalization with aminophenylene layers was also investigated in presence of hypophosphorous acid and iron powder. Effect of these homogeneous and heterogeneous reducing agents with respect to the formation of aryl layers at different thicknesses was discussed in detail on the basis of conventional hemolytic dediazoniation mechanism in combination with the XPS results
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