Search results for "Catalysis"
showing 10 items of 5944 documents
A critical review on latest innovations and future challenges of electrochemical technology for the abatement of organics in water
2023
Updated water directives and ambitious targets like the United Nations’ Sustainable Development Goals (SDGs) have emerged in the last decade to tackle water scarcity and contamination. Although numerous strategies have been developed to remove water pollutants, it is still necessary to enhance their effectiveness against toxic and biorefractory organic molecules. Comprehensive reviews have highlighted the appealing features of the electrochemical technologies, but much progress has been made in recent years. In this timely review, a critical discussion on latest innovations and perspectives of the most promising electrochemical tools for wastewater treatment is presented. The work describes…
Thermal 1,6-Electrocyclization Reactions of Acceptor-Substituted 2,3-Divinyl-1H-indoles Yielding Functionalized Carbazoles
1990
Three new synthetic procedures for and thermal 1,6-electrocyclizations of acceptor-substituted 2,3-divinyl-1H-indoles leading to functionalizing carbazoles are described. The scope and limitations as well as some mechanistic aspects of the methodologies are discussed. The key strategies employed include Pd(II)-catalyzed coupling and Wittig procedures.
Electrochemical synthesis of benzoxazoles from anilides - a new approach to employ amidyl radical intermediates.
2017
A novel electrochemical method for the synthesis of benzoxazoles from readily available anilides is reported. Various functionalities are tolerated and good yields can be achieved. By employing common electrode materials and a simple constant current protocol, this method is an attractive new alternative to conventional pathways.
Twofold Electrochemical Amination of Naphthalene and Related Arenes
2017
The twofold, electrochemical amination reaction of polycyclic arenes, e.g. naphthalene (4), via Zincke intermediates is demonstrated for the first time. The installation of the nitrogen functionalities occurs regioselectively in positions 1 and 5 of naphthalene (4). The key for this electro-conversion is boron-doped diamond as anode material. The method of the multi-amination reaction is expanded to other aromatic substrates. A detailed study is provided, covering electrolysis parameters, e.g. anode material, electrolyte system, current density, separator, etc. Despite the moderate yields, this approach offers the first direct electro-synthetic access to diaminated products.
Simple and scalable electrochemical synthesis of 2,1-benzisoxazoles and quinoline N-oxides.
2019
Cathodic reduction of the nitro moiety and subsequent intramolecular cyclization affords different substituted 2,1-benzisoxazoles and quinoline N-oxides. This methodology allows the synthesis of two different types of heterocycles from common simple starting materials, using electrons as a sole reagent for this transformation. The electrolysis can be conducted in a very simple undivided electrolysis cell under constant current conditions. This permits working on a larger scale compared to other electrochemical methodologies and represents a significant advantage.
Selective and Scalable Dehydrogenative Electrochemical Synthesis of 3,3′,5,5′-Tetramethyl-2,2′-biphenol
2019
3,3′,5,5′-Tetramethyl-2,2′-biphenol is a compound of high technical significance, as it exhibits superior properties as building block for ligands in the transition-metal catalysis. However, side reactions and overoxidation are challenging issues in the conventional synthesis of this particular biphenol. Here, an electrochemical method is presented as powerful and sustainable alternative to conventional chemical strategies, which gives good yields up to 51%. Despite using inexpensive and well-available bromide-containing supporting electrolytes, the issue of bromination and general byproduct formation is effectively suppressed by adding water to the electrolyte. Additionally, the scalabilit…
Synthesis ofmeta-Terphenyl-2,2′′-diols by Anodic C−C Cross-Coupling Reactions
2016
The anodic C-C cross-coupling reaction is a versatile synthetic approach to symmetric and non-symmetric biphenols and arylated phenols. We herein present a metal-free electrosynthetic method that provides access to symmetric and non-symmetric meta-terphenyl-2,2''-diols in good yields and high selectivity. Symmetric derivatives can be obtained by direct electrolysis in an undivided cell. The synthesis of non-symmetric meta-terphenyl-2,2''-diols required two electrochemical steps. The reactions are easy to conduct and scalable. The method also features a broad substrate scope, and a large variety of functional groups are tolerated. The target molecules may serve as [OCO](3-) pincer ligands.
Metal- and reagent-free highly selective anodic cross-coupling reaction of phenols.
2014
The direct oxidative cross-coupling of phenols is a very challenging transformation, as homo-coupling is usually strongly preferred. Electrochemical methods circumvent the use of oxidizing reagents or metal catalysts and are therefore highly attractive. Employing electrolytes with a high capacity for hydrogen bonding, such as methanol with formic acid or 1,1,1,3,3,3-hexafluoro-2-propanol, a direct electrolysis in an undivided cell provides mixed 2,2′-biphenols with high selectivity. This mild method tolerates a variety of moieties, for example, tert-butyl groups, which are not compatible with other strong electrophilic media but vital for later catalytic applications of the formed products.
CO2 turned into a nitrogen doped carbon catalyst for fuel cells and metal–air battery applications
2021
Heteroatom doped metal-free catalysts are one of the most promising replacements for platinum for the alkaline oxygen reduction reaction (ORR). Due to the lack of metal atoms, they are extremely stable and environmentally friendly. However, production of carbon nanomaterials can have a very high CO2 footprint. In this study, we present ORR catalysts made directly from CO2via molten salt CO2 electrolysis. The deposited carbon powder is doped with nitrogen using pyrolysis in the presence of dicyandiamide. The effect of molten carbonate electrolyte composition towards the final ORR activity in 0.1 M KOH is studied. A thorough physico-chemical study of the starting carbons and N-doped catalysts…
Electrochemistry as an Attractive and Effective Tool for the Synthesis and Immobilization of Porphyrins on an Electrode Surface
2014
Magnesium(II) 10-phenyl-5,15-p-ditolylporphyrin is easily and cleanly transformed by electrolysis. A nitro group is first introduced at the free meso position by anodic substitution. Hydrogenation into the amine is then carried out electrocatalytically under ambient conditions with water as a hydrogen supplier. The synthesized porphyrin under the nickel(II) form can be covalently grafted onto a platinum electrode by electrochemical reduction of the diazonium cation, generated in situ by a reaction of the nickel(II) aminoporphyrin with sodium nitrite and trifluoroacetic acid. The electrosynthesized thin film gives an electrochemical response typical of a porphyrin material. Films grown under…