Revealing the solid-state reaction process among multiphase multicomponent ceramic during ablation

Multiphase design is a promising approach to achieve superior ablation resistance of multicomponent ultra-high temperature ceramic,while understanding the ablation mechanism is the foundation.Here,through investigating a three-phase multicomponent ceramic consisting of Hf-rich carbide,Nb-rich carbide,and Zr-rich silicide phases,we report a newly discovered solid-state reaction process among multiphase multicomponent ceramic during ablation.It was found that this solid-state reaction occurred in the matrix/oxide scale interface region.In this process,metal cations are counter-diffused between the multicomponent phases,thereby resulting in their composition evolution,which allows the multicomponent phases to exist stably under a higher oxygen partial pressure,leading to the improvement of thermodynamic stability of three-phase multicomponent ceramic.Additionally,this solid-state reaction process appears synergistic with the preferential oxidation behavior among the oxide scale in enhancing the ablation performance.

Recent advances in fixation of CO_(2) into organic carbamates through multicomponent reaction strategies

Carbon dioxide(CO_(2)) is the main greenhouse gas and also an ideal C1 feedstock in organic synthesis because it is abundant,nontoxic,nonflammable,and renewable.The synthesis of organic carbamates using CO_(2) as a phosgene alternative has attracted extensive attention because of the importance of carbamates in organic synthesis and in the pharmaceutical and agrochemical industries.In recent decades,many multicomponent reaction strategies have been designed for constructing different types of organic carbamate molecules.Most of these methods rely on the in situ generation of carbamate anions from CO_(2) and amines,followed by reactions with other coupling partners.Synthetic strategies for acyclic carbamates include nucleophile‐electrophile coupling,nucleo‐phile‐nucleophile oxidative coupling,difunctionalization of unsaturated hydrocarbons,and C–H bond functionalization.Strategies for the synthesizing cyclic carbamates include carboxylative cyclization of in situ‐generated unsaturated amines and difunctionalization of unsaturated amines with CO_(2) and other electrophilic reagents.This review summarizes the recent advances in the synthesis of organic carbamates from CO_(2) using different multicomponent reaction strategies.Future perspectives and challenges in the incorporation of CO_(2) into carbamates are also presented.

Multicomponent Reaction in Ionic Liquid: A Novel and Green Synthesis of 1, 4-Dihydropyridine Derivatives

An efficient and green method for the synthesis of 1, 4-dihydropyridine derivatives mediated in an ionic liquid, [bmim][BF4], through a four-component condensation process of aldehydes, 1, 3-dione, Meldrum＇s acid and ammonium acetate is disclosed in this paper.

One-pot Multicomponent Synthesis, Spectroscopy, Crystal Structures and Theoretical Calculations of 3-Cyano-4-(4-hydroxy-3-methoxyphenyl)-6-phenyl-2(1H)-pyridinone and 3-Cyano-4-chlorophenyl-6-(4-tolyl)-2(1H)-pyridinone

Pyridinone derivatives are of great interest in medicinal chemistry where they were found to be potent to various diseases. Their metal complexes added more value to their applications. Here, we have synthesized two 2-pyridinone derivatives(3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-phenyl-2(1 H)-pyridinone and 3-cyano-4-chlorophenyl-6-(4-tolyl)-2(1 H)-pyridinone) using one-pot multicomponent system. They were well characterized using spectroscopic techniques like nuclear magnetic resonance(NMR-1 H & 13 C), Fourier transform infrared(FT-IR) and UV/Vis spectroscopy. The final structures were determined using single-crystal X-ray diffraction technique which helps us to determine their geometries. Density functional theory(DFT) and time-dependent density functional theory(TD-DFT) with suitable basis-sets of calculations have correctly simulated these spectroscopic parameters. The intramolecular charge transfer(ICT) of both substrates has been discussed using natural bond orbital(NBO) technique. Molecular electrostatic potential(MEP) surfaces showed their reactive locations for intermolecular charge transfer. Compared to p-nitroaniline(pNA), both substrates were shown to have substantial molecular hyperpolarizability.

AN ENGINEERING MODEL FOR MULTICOMPONENT REVERSIBLE REACTION NETWORK

The treatment of a multicomponent reversible reaction network is extremely complicated because largenumber of rate constants must be precisely determined and because the calculation based on these rateconstants is tedious.In order to reduce the degrees of freedom of the process,the authors propose a methodin which the reactor and the separator are regarded as a whole.Based on this approach,an N-componentreversible reaction system can be dealt with as a two—component system.Consequently,a simple and ac-cessible way of the apparent rate determination is suggested.For fiist-order reactions,an explicit,simplifiedexpression has been derived for both lumped and distributed parameter reaction systems.

New Method for Preparation of 1-Amidoalkyl-2-Naphthols via Multicomponent Condensation Reaction Utilizing Tetrachlorosilane under Solvent Free Conditions

An efficient and direct procedure for the synthesis of amidoalkylnaphthol derivatives employing a multi-component and one-pot condensation reaction of 2-naphthol, aromatic aldehyde and ace-tonitrile in the presence of tetrachlorosilane (TCS). A binary reagent from (TCS)/ZnCl2 was used upon applying benzonitrile.

Multicomponent transition metal phosphide for oxygen evolution

Transition metal phosphides(TMPs)have exhibited decent performance in an oxygen evolution reaction(OER),which is a kinetic bottleneck in many energy storages and conversion systems.Most reported catalysts are composed of three or fewer metallic components.The inherent complexity of multicomponent TMPs with more than four metallic components hinders their investigation in rationally designing the structure and,more importantly,comprehending the component-activity correlation.Through hydrothermal growth and subsequent phosphor-ization,we reported a facile strategy for combining TMPs with tunable elemental compositions(Ni,Fe,Mn,Co,Cu)on a two-dimensional ti-tanium carbide(MXene)flake.The obtained TMPs/MXene hybrid nanostructures demonstrate homogeneously distributed elements.They ex-hibit high electrical conductivity and strong interfacial interaction,resulting in an accelerated reaction kinetics and long-term stability.The res-ults of different component catalysts’OER performance show that NiFeMnCoP/MXene is the most active catalyst,with a low overpotential of 240 mV at 10 mA·cm−2,a small Tafel slope of 41.43 mV·dec−1,and a robust long-term electrochemical stability.According to the electrocata-lytic mechanism investigation,the enhanced NiFeMnCoP/MXene OER performance is due to the strong synergistic effect of the multi-ele-mental composition.Our work,therefore,provides a scalable synthesis route for multi-elemental TMPs and a valuable guideline for efficient MXene-supported catalysts design.

Cobalt-based multicomponent nanoparticles supported on N-doped graphene as advanced cathodic catalyst for zinc-air batteries

To improve the efficiency of cathodic oxygen reduction reaction(ORR)in zinc-air batteries(ZABs),an adsorption-complexation-calcination method was proposed to generate cobalt-based multicomponent nanoparticles comprising Co,Co_(3)O_(4)and CoN,as well as numerous N heteroatoms,on graphene nanosheets(Co/Co_(3)O_(4)/CoN/NG).The Co/Co_(3)O_(4)/CoN nanoparticles with the size of less than 50 nm are homogeneously dispersed on N-doped graphene(NG)substrate,which greatly improve the catalytic behaviors for ORR.The results show that the half-wave potential is as high as 0.80 V vs.RHE and the limiting current density is 4.60 mA·cm^(−2),which are close to those of commercially available platinum/carbon(Pt/C)catalysts.Applying as cathodic catalyst for ZABs,the battery shows large specific capacity and open circuit voltage of 843.0 mAh∙g^(−1) and 1.41 V,respectively.The excellent performance is attributed to the efficient two-dimensional structure with high accessible surface area and the numerous multiple active sites provided by highly scattered Co/Co_(3)O_(4)/CoN particles and doped nitrogen on the carbon matrix.

Synthesis of 2,4-Diarylcyclooctenopyridines with One-pot Four-component Reactions

An efficient one-pot four-component reaction has been developed for the synthesis of 2,4-diarylcyclooctenopyridines, in moderate yields. This route is an effective modified two-step synthesis of Krohnke pyridine and involves a four-component tandem reaction of pyridinium bromide with aromatic aldehydes and cyclooctanone in a system of NHaOAc/HOAc under microwave irradiation.

Microwave-assisted one-pot synthesis of 3-substituted-3,4-dihydrocoumarins via tendem Konevenagel and Hantzsch reactions

A convenient route for the synthesis of 3,4-dihydrocoumarin derivates from salicylaldehyde derivates and 1,3-dicarbonyl compounds under solvent-free microwave irradiation conditions was described. In this way, a range of compounds was obtained in moderate to good yields in a short reaction time.

One-Pot Reaction of Aldehydes,α-Haloketones and (Phenylsulfonyl)acetonitrile Promoted by SmI3

One-pot reaction of aldehydes, ?haloketones and (phenylsulfonyl)acetonitrile promoted by SmI3 proceeded smoothly to give 1-cyano-1-phenylsulfonyl-2-aryl-3-aroyl-propane derivatives in moderate to good yields.

Bismuth (III) Triflate Catalyzed Multicomponent Synthesis of 2,4,5-Trisubstituted Imidazoles

Substituted imidazoles are of interest because of their useful biological activities. While several methods have been developed for the synthesis of such compounds, some of the reported methods utilize corrosive or toxic catalysts. We report a bismuth (III) triflate catalyzed multicomponent synthesis of 2,4,5-trisubstituted imidazoles. Bismuth (III) compounds are attractive from a green chemistry perspective because they are remarkably non-toxic and non-corrosive. Multicomponent syntheses save time and generate less waste.

Bismuth (III) Chloride Catalyzed Multicomponent Synthesis of Substituted Hexahydroimidazo[1, 2-<i>a</i>]Pyridines

The synthesis of nitrogen containing heterocycles is of particular interest in the pharmaceutical industry due to the range of biological activities exhibited by such compounds. Their synthesis using multicomponent reactions saves steps and minimizes waste generation. The bismuth (III) chloride multicomponent synthesis of a series of hexahydroimidazo[1, 2-a]pyridines is reported. Bismuth (III) compounds are especially attractive from a green chemistry perspective because they are remarkably nontoxic, non-corrosive and relatively inexpensive. The reported method avoids chromatography and an aqueous waste stream to afford the products in a very mass efficient manner.

Facile One-Pot Synthesis of Novel Hexahydro-2-quinolinecarboxylic Acids under Solvent-Free Reaction Conditions

A simple and fastthree-component synthesis of new and biologically active hexahydro-2-quinolinecarboxylic acid scaf-fold 4 was carried out using cyclocondensation reaction of arylmethylidenepyruvic acids 1, 1,3-cyclohexandiones 2 and ammonium acetate 3 under solvent-free conditions and at room temperature. This protocol has the advantages of facility, easy work-up, high yields, short reaction time and environmentally friendly character.

A New One-Pot Synthesis of Macroheterocycles Using Mannich Reaction

Three N,N-heterylmethyl derivates of diaza-18-crown-6(I) are readily prepared by the reaction of (I) with paraformaldehyde and heterocyclic compounds in dry benzene.

Bismuth (III) Triflate Catalyzed Multicomponent Synthesis of 2,4,5-Trisubstituted Imidazoles

Substituted imidazoles are of interest because of their useful biological activities. While several methods have been developed for the synthesis of such compounds, some of the reported methods utilize corrosive or toxic catalysts. We report a bismuth (III) triflate catalyzed multicomponent synthesis of 2,4,5-trisubstituted imidazoles. Bismuth (III) compounds are attractive from a green chemistry perspective because they are remarkably non-toxic and non-corrosive. Multicomponent syntheses save time and generate less waste.

Switchable Multicomponent Cyclization Reactions to Access Fluoroalkylated Dihydropyrimidines and Pyrimidines under Solvent-Free Conditions

Comprehensive Summary The development of switchable solvent-free multicomponent reactions to build high-value-added products is an important demand for organic synthesis.Herein,we detailed the successful implementation of a switchable strategy for the construction of diverse 4-fluoroalkyl-1,4-dihydropyrimidines and 4-fluoroalkyl-pyrimidines via a solvent/additive-free[3+2+1]annulation,starting from readily available enamines,trifluoroacetaldehyde hydrate or 1-ethoxy-2,2-difluoroethanol and amidines hydrochloride.This reaction conforms to the concept of green synthesis,and provides a new avenue to access valuable fluorinated heterocycles.

Functionalization of covalent organic frameworks via multicomponent reactions

Functionalized covalent organic frameworks(COFs)represent a fascinating class of porous materials that have attracted widespread interest due to their modifiable structures and impressive potential applications.However,the construction of functionalized COFs remains difficult as it requires simultaneous consideration of robust linkages,diversified structures,and tailorable functionalities.Recently,the introduction of multicomponent reactions(MCRs)into COF synthesis opens new avenues for creating highly stable and function-oriented COF materials,marking a significant advance in the development of COFs.This minireview summarizes the types of MCRs used in COF synthesis,highlights the functionalization strategies of COFs via MCRs,and provides insights on the key challenges and future frontiers in this field.

MCM-41 anchored sulfonic acid (MCM-41-R-SO_3H):A mild,reusable and highly efficient heterogeneous catalyst for the Biginelli reaction

An efficient three-component synthesis of 3,4-dihydropyrimidinones using MCM-41 anchored sulfonic acid （MCM-41-R-SO3H） as a mild, heterogeneous catalyst for Biginelli reaction in CH3CN under reflux condition is described.

Hetero MOF-on-MOF-derived carbon nanotube interconnected nitrogen-doped carbon-encapsulated FeNi/FeF2 for efficient oxygen evolution reaction

Heterostructures derived from metal–organic frameworks(MOFs)with multicomponent synergism are significant in the energy conversion and catalysis reactions.Herein,we demonstrated such an efficient catalyst with the structure of self-catalyzed nitrogen-doped carbon nanotube interconnected FeNi/FeF2 derived from hetero-zeolite imidazolate frameworks 8(ZIF-8)on Fe2Ni MIL(MIL represents Materials of Institut Lavoisier)for oxygen evolution reaction.The obtained catalyst showed efficient synergism of the multicomponents,high polarity,more active sites exposure,increased intrinsic activity,and improved conductivity and stability by a carbon interconnected and confined structure as revealed by the spectroscopic analysis and electrochemical measurements.It required an overpotential of only ca.240mV(no iR correction)to reach the current density of 10mAcm^(−2) in a KOH solution when loaded on an inert glass carbon electrode,much better than similar kinds of catalysts.The improved catalytic performance can be well correlated to the structural transformation step by step from different MOFs to their derivatives by subsequent carbonation and fluorination.Because of the above-mentioned structural advantages,good catalysis performance of high activity and stability,faster catalytic kinetics,and facile active phase formation were observed compared to those of other similar materials.This work offers a new platform of derivatives from hetero MOF-on-MOF for catalysis reactions.