Sustainable Generation of Ni(OH)2 Nanoparticles for the Green Synthesis of 5-Substituted 1 H-Tetrazoles:A Competent Turn on Fluorescence Sensing of H2O2

A mutually correlated green protocol has been devised that originates from a sustainable production of β-Ni(OH)2 nanoparticles which is used for an efficient catalytic synthesis of versatile substituted tetrazoles, under mild reaction conditions in water via a simple, one-pot, eco-friendly method. The synthesis is followed by derivatization into a highly fluorescence active compound 9-(4-(5-(quinolin-2-yl)-1H-tetrazol-1-yl)phenyl)-9H-carbazole that can be used at tracer concentrations (0.1 μM) to detect as well as quantify hydrogen peroxide down to 2 μM concentration. The nanocatalyst was synthesized by a simple, proficient, and cost-effective methodology and characterized thoroughly by UV-vis absorption and Fourier transform infrared spectra, N2 adsorption/desorption, high resolution transmission electron microscopy, powder X-ray diffraction pattern, field emission scanning electron microscopy, and thermogravimetric analysis. Broad substrate scope, easy handling, higher efficiency, low cost, and reusability of the catalyst are some of the important features of this heterogeneous catalytic system. The strong analytical performance of the resultant derivative in low-level quantification of potentially hazardous hydrogen peroxide is the key success of the overall green synthesis procedure reported here

Heterogeneous Route for the One-Pot Synthesis of N‑Arylamides from Aldoximes and Aryl Halides Using the CuO/Carbon Material

Metal oxide nanoparticles (NPs) stabilized by porous carbon materials (PCMs) are very promising for catalysis. In this work, monodispersed small and stable copper oxide (CuO) NPs were prepared with an average size of 10–20 nm without using any capping agent and then these NPs were encapsulated into porous carbon. The chemical and structural properties of the CuO/PCM material were characterized by powder X-ray diffraction, electron microscopy, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and nitrogen sorption. The obtained CuO/PCM nanocatalytic system has been used for the synthesis of N-arylamides from the reaction of aldoximes and aryl halides. Generally, copper­(II) salt was used for the preparation of amides from aldoximes using some ligands and bases, but harsh reaction condition, stoichiometric amount of metal, and lack of recyclability limit their applications in industry. An alternative method is the use of heterogeneous catalysts. More importantly, these heterogeneous catalysts could be easily recycled and reused, showing potential application in organic synthesis

New Hybrid Iron Phosphonate Material as an Efficient Catalyst for the Synthesis of Adipic Acid in Air and Water

A new organic–inorganic hybrid iron phosphonate material (FePO-1-2) has been synthesized hydrothermally using etidronic acid (1-hydroxyethylidene-1,1-diphosphonic acid) as an organophosphorus precursor. Under optimized reaction conditions the synthesis has been carried out hydrothermally for 3 days at 180 °C temperature at near neutral pH. The material has been characterized thoroughly by various techniques and its crystal structure has been indexed to a new orthorhombic phase with unit cell parameters of <i>a</i> = 10.995 Å, <i>b</i> = 10.395 Å, <i>c</i> = 11.793 Å, and α = β = γ = 90°. The considerably good Brunauer–Emmett–Teller (BET) surface area of 236 m² g^–1, pore volume of 0.229 cm³ g^–1, and robust nature of FePO-1-2 have motivated us to explore its catalytic activity in liquid phase partial oxidation reactions under green conditions. FePO-1-2 exhibits excellent catalytic activity (96% product selectivity, 72% conversion) for selective liquid phase oxidation of cyclohexanone to adipic acid in the presence of molecular O₂ under atmospheric pressure and in aqueous medium. This selective liquid (aqueous) phase oxidation pathway is highly green and sustainable as it does not involving any need of nitric acid, initiator, peroxides, and other organic solvents

Sustainable Generation of Ni(OH)₂ Nanoparticles for the Green Synthesis of 5‑Substituted 1<i>H</i>‑Tetrazoles: A Competent Turn on Fluorescence Sensing of H₂O₂

A mutually correlated green protocol has been devised that originates from a sustainable production of β-Ni­(OH)₂ nanoparticles which is used for an efficient catalytic synthesis of versatile substituted tetrazoles, under mild reaction conditions in water via a simple, one-pot, eco-friendly method. The synthesis is followed by derivatization into a highly fluorescence active compound 9-(4-(5-(quinolin-2-yl)-1<i>H</i>-tetrazol-1-yl)­phenyl)-9<i>H</i>-carbazole that can be used at tracer concentrations (0.1 μM) to detect as well as quantify hydrogen peroxide down to 2 μM concentration. The nanocatalyst was synthesized by a simple, proficient, and cost-effective methodology and characterized thoroughly by UV–vis absorption and Fourier transform infrared spectra, N₂ adsorption/desorption, high resolution transmission electron microscopy, powder X-ray diffraction pattern, field emission scanning electron microscopy, and thermogravimetric analysis. Broad substrate scope, easy handling, higher efficiency, low cost, and reusability of the catalyst are some of the important features of this heterogeneous catalytic system. The strong analytical performance of the resultant derivative in low-level quantification of potentially hazardous hydrogen peroxide is the key success of the overall green synthesis procedure reported here

Biogenic Nano-CuO-Catalyzed Facile C–N Cross-Coupling Reactions: Scope and Mechanism

We demonstrate here a green and efficient biogenic synthesis of copper­(II) oxide nanoparticles using easily available <i>Ocimum Sanctum</i> leaf extract at room temperature. The biogenic copper oxide nanoparticles have shown excellent activity on N-arylation of cyclic and acyclic amides with aryl and styryl halides. Broad substrate scope, excellent functional group tolerance, and high yields were observed. This protocol is also extended for the N-arylation of substituted aryl amines and nitrogen heterocycles including pyrole, indole, imidazole, benzimidazole, and carbazole. The catalyst was characterized by EPR, UV, FT-IR, BET, AAS, TGA analysis, XPS, XRD, and HR-TEM