Three-Component Reaction of 3-Arylidene-3H-Indolium Salts, Isocyanides, and Alcohols

A novel isocyanide-based multicomponent synthesis of alkyl aryl(indol-3-yl)acetimidates has been established. Starting from aryl(indol-3-yl)methylium tetrafluoroborates, aromatic isocyanides and alcohols, the imidates were obtained in moderate to very good yields. Consecutive four-component synthesis of the above mentioned imidates from N-alkylindoles, aromatic aldehydes, aromatic isocyanides and alcohols was also proposed. In addition, it was shown that in the presence of water, aryl(indol-3-yl)methylium tetrafluoroborates reacted with isocyanides to furnish aryl(indol-3-yl)acetamides

Methyl (2E)-3-[3-Benzyl-2-(3-methoxy-3-oxoprop-1-yn-1-yl)-2-(1-naphthyl)imidazolidin-1-yl]acrylate

Compounds with propargylamine moiety are useful synthetic precursors of several important classes of nitrogen-containing heterocycles. The title compound, methyl (2E)-3-[3-benzyl-2-(3-methoxy-3-oxoprop-1-yn-1-yl)-2-(1-naphthyl)imidazolidine-1-yl]acrylate, has been prepared by domino-reaction, employing easily available 1-benzyl-2-(1-naphthyl)-4,5-dihydro-1H-imidazole and methyl propiolate in a high 92% yield. The structure of title compound was determined using 1H-NMR, 13C-NMR, UV, FT-IR and HRMS (High-Resolution Mass Spectrometry)

1-Benzyl-2-(thien-2-yl)-4,5-dihydro-1H-imidazole

Imidazolines are a valuable class of organic compounds, namely ligands of imidazoline receptors, chiral ligands for metal catalysis, synthetic intermediates. The title compound has been prepared through a modified procedure, employing N-benzylethylenediamine and thiophene-2-carbaldehyde under the action of N-bromosuccinimide (NBS) in dichloromethane (DCM) in a good 78% yield

Three-Component Reactions of 3-Arylidene-3H-Indolium Salts, Isocyanides and Amines

A multicomponent reaction of isocyanides with aryl(indol-3-yl)methylium salts and amines has been found. A series of aryl(indol-3-yl)acetimidamides was obtained in up to 96% yields. In the case of ethyl isocyanoacetate, the reaction is followed by cyclization to form 3,5-dihydro-4H-imidazol-4-one derivatives

A Novel High-Performance Anode Material with an Enlarged Potential Window for a Hybrid Energy Storage System

Cobalt-iron (CoFe) layered double hydroxides (LDHs) have received much interest for supercapacitors (SCs) because of their ion-insertable layer structure. However, there is still a need for more effort to increase their potential window and overall electrochemical energy storage capability as SC electrodes. In this work, we present a straightforward approach to synthesizing CoFe-LDHs on zinc oxide seeded carbon cloth (ZnO@CC) via a one-step hydrothermal reaction; the obtained electrode is denoted as CoFe-LDH@ZnO@CC. The electrochemical energy storage properties of CoFe-LDH@ZnO@CC are tested as an anode material using a three-electrode setup for SC applications in 1 M Na2SO4 electrolyte. It can operate in a wider potential window reaching up to 1.6 V, exceeding most previously reported anode materials. The CoFe-LDH@ZnO@CC displayed capacitive charge storage accounting for 76% of the total charge stored at 20 mV/s. The CoFe-LDH@ZnO@CC anode delivered a maximum capacitance of 299.8 F/g at 2 A/g, outstanding cycle stability, and retained 97.7% of the initial capacitance value for 5000 cycles at 16 A/g. This study introduces a new strategy for structurally designing electroactive materials for energy storage devices, which might be useful as an anode for SCs

A Novel High-Performance Anode Material with an Enlarged Potential Window for a Hybrid Energy Storage System

Cobalt-iron (CoFe) layered double hydroxides (LDHs) have received much interest for supercapacitors (SCs) because of their ion-insertable layer structure. However, there is still a need for more effort to increase their potential window and overall electrochemical energy storage capability as SC electrodes. In this work, we present a straightforward approach to synthesizing CoFe-LDHs on zinc oxide seeded carbon cloth (ZnO@CC) via a one-step hydrothermal reaction; the obtained electrode is denoted as CoFe-LDH@ZnO@CC. The electrochemical energy storage properties of CoFe-LDH@ZnO@CC are tested as an anode material using a three-electrode setup for SC applications in 1 M Na2SO4 electrolyte. It can operate in a wider potential window reaching up to 1.6 V, exceeding most previously reported anode materials. The CoFe-LDH@ZnO@CC displayed capacitive charge storage accounting for 76% of the total charge stored at 20 mV/s. The CoFe-LDH@ZnO@CC anode delivered a maximum capacitance of 299.8 F/g at 2 A/g, outstanding cycle stability, and retained 97.7% of the initial capacitance value for 5000 cycles at 16 A/g. This study introduces a new strategy for structurally designing electroactive materials for energy storage devices, which might be useful as an anode for SCs