Electrocarboxylation of carbon dioxide(CO_(2))using organic substrates has emerged as a promising method for the sustainable synthesis of value-added carboxylic acids due to its renewable energy source and mild reacti...Electrocarboxylation of carbon dioxide(CO_(2))using organic substrates has emerged as a promising method for the sustainable synthesis of value-added carboxylic acids due to its renewable energy source and mild reaction conditions.The reactivity and product selectivity of electrocarboxylation are highly dependent on the cathodic behavior,involving a sequence of electron transfers and chemical reactions.Hence,it is necessary to understand the cathodic reaction mechanisms for optimizing reaction performance and product distribution.In this work,a review of recent advancements in the electrocarboxylation of CO_(2)with organic substrates based on different cathodic reaction pathways is presented to provide a reference for the development of novel methodologies of CO_(2)electrocarboxylation.Herein,cathodic reactions are particularly classified into two categories based on the initial electron carriers(i.e.,CO_(2)radical anion and substrate radical anion).Furthermore,three cathodic pathways(ENE(N),ENED,and EDEN)of substrate radical anion-induced electrocarboxylation are discussed,which differ in their electron transfer sequence,substrate dissociation,and nucleophilic reaction,to highlight their implications on reactivity and product selectivity.展开更多
Carboxylation of aromatics by CO2 to generate corresponding carboxylic acids is recently providing a novel approach to utilize the green gas CO2, in which the activation of CO2 is the key procedure. Among the many cat...Carboxylation of aromatics by CO2 to generate corresponding carboxylic acids is recently providing a novel approach to utilize the green gas CO2, in which the activation of CO2 is the key procedure. Among the many catalytic systems employed in the carboxylation, the concept of “Frustrated Lewis Pairs” (FLPs) was scarcely mentioned, which perform excellently in activating small molecules like CO2. The FLPs are combinations of Lewis acids and Lewis bases which failed to form adducts due to their bulky steric congestion. In this paper, we first attempted various Si/Al Based FLPs to catalyze the carboxylation of aromatics through the activation of CO2, and a good yield of 62% - 97% was obtained. The reaction mechanism was proposed, involving the activation of CO2 mainly contributed by AlCl3 in cooperation with organosilane, forming an intermediate consisting of CO2, AlCl3, and R4Si, as well as the subsequent electrophilic attack to aromatics, thus to promote the carboxylation reaction.展开更多
A feasible synthesis route is developed for achieving the direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten state.The effects of reaction factors...A feasible synthesis route is developed for achieving the direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten state.The effects of reaction factors on the carboxylate yield are investigated in the preliminary screening experiments,and the phase behavior analysis of the reaction medium is detected through the thermal characterization analysis of insitu high temperature X-ray diffraction measurement(in-situ XRD).The application of response surface methodology(RSM)based on the Box-Behnken design(BBD)is conducted to investigate the effect of the reaction parameters,such as reaction temperatu re,carbonate proportion,CO_(2) pressure and thiophene amount,on the product yield.The regressed second-order polynomial model equation well correlates all the independent variables.The analysis of variance(ANOVA)results reveal that the quadratic effect of reaction temperature is the most effective parameter in this carboxylation reaction owing to it’s the highest contribution to the sum of square(30.18%).The optimum reaction conditions for maximum product yield are the reaction temperature of 287℃,carbonate proportion of 32.20%,CO_(2) pressure of 1.0MPa and thiophene amount of 9.35 mmol.Operating under these selected experimental conditions,a high product yield(50.98%)can be achieved.展开更多
A feasible synthesis route is devised for realizing direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten medium.The effects of reaction factors on p...A feasible synthesis route is devised for realizing direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten medium.The effects of reaction factors on product yield are investigated,and the phase behavior analysis of the reaction medium is detected through the thermal characterization techniques.Product yield varies with the alternative carboxylate co-salts,which is attributed to the difference in deprotonation capacity caused by the base effect within the system.Besides,the detailed mechanism of this carbonate-promoted carboxylation reaction is studied,including two consecutive steps of the formation of carbanion through breaking the C-H bond(s)via the carbonate and the nucleophile attacking the weak electrophile CO_(2) to form C-C bond(s).The activation energy barrier in C-H activation step is higher than the following CO_(2) insertion step whether for the formation of the mono-and/or di-carboxylate,which is in good agreement with that of kinetic isotope effect(KIE)experiments,indicating that the C-H deprotonation is slow and the forming presumed carbanion reacts rapidly with CO_(2).Both the activation energy barriers in deprotonation steps are the minimal for the cesium cluster system since there have the weak the cesium Cs-heteroatom S(thiophene)and Cs-the broken proton interactions compared to the K2CO3 system,which is likely to enhance the acidity of C-H bond,lowering the C-H activation barrier.Besides,these mechanistic insights are further assessed by investigating base and C-H substrate effects via replacing Cs2CO3 with K2CO3 and furoate(la)with thiophene monocarboxylate(1b)or benzoate(1c).展开更多
Manganese(Ⅲ) meso-tetraphenylporphyrin acetate [Mn(TPP)OAc] served as an effective catalyst for the oxidative decarboxylation of carboxylic acids with (diacetoxyiodo)benzene [PhI(OAc)2] in CH2CI2-H2O(95:5, ...Manganese(Ⅲ) meso-tetraphenylporphyrin acetate [Mn(TPP)OAc] served as an effective catalyst for the oxidative decarboxylation of carboxylic acids with (diacetoxyiodo)benzene [PhI(OAc)2] in CH2CI2-H2O(95:5, volume ratio). The aryl substituted acetic acids are more reactive than the less electron rich linear carboxylic acids in the presence of catalyst Mn(TPP)OAc. In the former case, the formation of carbonyl products was complete within just a few minutes with 〉97% selectivities, and no further oxidation of the produced aldehydes was achieved under these catalytic conditions. This method provides a benign procedure owing to the utilization of low toxic(diacetoxyiodo) benzene, biologically relevant manganese porphyrins, and carboxylic acids.展开更多
A direct regioselective preparation of 2-hydroxynaphthalene-6-carboxylic acid, a useful industrial intermediate of aro-matic polyester from 2-naphthol was conducted by use of excess amount of K2CO3 (10-fold molar to 2...A direct regioselective preparation of 2-hydroxynaphthalene-6-carboxylic acid, a useful industrial intermediate of aro-matic polyester from 2-naphthol was conducted by use of excess amount of K2CO3 (10-fold molar to 2-naphthol) under supercritical CO2 at 10 MPa and 473 K. The obtained yield under this condition was ca. 20 mol% to 2-naphthol. The further investigations may provide an alternative process to the conventional Kolbe-Schmitt reaction, because of no use of strong alkali and recoverability of K2CO3. Theoretical explanation about the regioselectivity was achieved by means of DFT calculations.展开更多
The mechanism and the final outcome of the Knoevenagel-Doebner reaction are discussed. The condensation reaction between different hydroxy-substituted aromatic aldehydes and malonic acid is performed using piperidine ...The mechanism and the final outcome of the Knoevenagel-Doebner reaction are discussed. The condensation reaction between different hydroxy-substituted aromatic aldehydes and malonic acid is performed using piperidine as organocatalyst. The key role of the catalyst is clearly pointed out during the decarboxylation of ferulic acid, without the use of a strong decarboxylating agent, leading to a 4-vinylphenol derivative. Based on the results obtained, the studied pathway may be important in the understanding of vinylphenol production during malting and brewing of wheat and barley grains. Finally, changing the solvent of the reaction from pyridine to water in the Knoevenagel-Doebner reaction of 4-hydroxybenzaldehydes, dimerization of resulting styrene derivatives is observed. These results can be of interest also in the field of food chemistry, since cinnamic acids are frequently found in fruits and vegetables used for human consumption.展开更多
The combination of a low cost source of Biofine's levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable co...The combination of a low cost source of Biofine's levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable compounds for transportation sector. The present review illustrates the development of different approaches to one–pot synthesis of fuel-like alkanes from lignocellulose derived carboxylic acids where particular focus is given to valeric acid consecutive decarboxylative coupling(ketonization) and ketone hydrodeoxygenation in a single reactor over one catalyst bed. The key factors that influence the catalytic performance on both ketonization and hydrodeoxygenation steps as well as their cross-influence will be clarified to provide insights for the design of more efficient catalysts for the one-pot transformation. Valeric acid is considered as a potential acid source from viewpoint of cost effectiveness and feasibility of such transformation with reasonable alkane yield. The both reaction mechanisms and kinetics will also be discussed to understand deeply how the selective C–C coupling and following C=O hydrogenation can be achieved.展开更多
Recently,significant research has been conducted on the conversion of carbon dioxide(CO_(2))into value-added chemicals.With the decreasing cost of clean electricity,electrochemical methods have emerged as potential ap...Recently,significant research has been conducted on the conversion of carbon dioxide(CO_(2))into value-added chemicals.With the decreasing cost of clean electricity,electrochemical methods have emerged as potential approaches for converting and fixing CO_(2).Organic electrochemical synthesis is a promising method for utilizing CO_(2)because it transforms CO_(2)into higher-value chemicals.This review introduces the research aspects of CO_(2)conversion and the mechanisms of CO_(2)organic electrocarboxylation reactions.Recent progress in electrocarboxylation with CO_(2)is discussed,considering organic substrates and cathode types under different reaction mechanisms.Finally,the challenges and prospects in this field are highlighted with the aim of further promoting the fundamental understanding of CO_(2)organic electrocarboxylation.展开更多
As an attractive C1 synthon,carbon dioxide(CO_(2))has been extensively used in organic synthesis to produce carboxylic acids.In this research,stereoselective electrochemical carboxylation ofα,β-unsaturated sulfones ...As an attractive C1 synthon,carbon dioxide(CO_(2))has been extensively used in organic synthesis to produce carboxylic acids.In this research,stereoselective electrochemical carboxylation ofα,β-unsaturated sulfones has been developed under transition-metal-free conditions.All the cinnamic acids and the derivatives are obtained selectively in the E-configuration.Besides,arylpropiolates also can be produced from alkynyl sulfones.展开更多
Difunctionalizing carboxylation of alkynes with CO_(2)is a sustainable and important strategy to generate valuable acrylate derivatives from both readily available starting materials.Such protocols,however,always suff...Difunctionalizing carboxylation of alkynes with CO_(2)is a sustainable and important strategy to generate valuable acrylate derivatives from both readily available starting materials.Such protocols,however,always suffer from the use of excess metallic reagents and transition metal residue.Herein,we report the first thio-carboxylation of alkynes with thiophenols and CO_(2),which is a visible-light-driven and transition metal-free process.In contrast to previous carboxylations of alkynes via two-electron activation of CO_(2),mechanistic and computational investigations suggest that the single-electron activation of CO_(2)is involved in the thio-carboxylation,rendering uniqueβ-carboxylation.The following cyclizing acylation affords important thiochromones efficiently.Moreover,the one-pot method features mild reaction conditions(room temperature,1 atmosphere of CO_(2)),high chemo-and regio-selectivity,easy scalability and facile derivatization of products to bioactive compounds.展开更多
Biomass,as the exclusive and abundant organic resources,is considered to be the promising renewable resource.Carboxylic acids are one of the many compounds that can be obtained from raw biomass.Decarboxylation of carb...Biomass,as the exclusive and abundant organic resources,is considered to be the promising renewable resource.Carboxylic acids are one of the many compounds that can be obtained from raw biomass.Decarboxylation of carboxylic acids into fuels and chemicals via electrochemical method at mild reaction condition has been studied for many years.The(non-)Kolbe reaction,one of the oldest organic electrochemical reactions,is the decarboxylation of carboxylic acids to produce alkanes,alcohols,esters,etc.And electrode materials influence the production of electrocatalytic decarboxylation products from carboxylic acids.Therefore,this work mainly reviews the recent advances in applications of anodic materials for(non-)Kolbe electrocatalytic decarboxylation of carboxylic acids.It discusses the reaction mechanism of(non-)Kolbe electrolytic reaction,and the electrocatalytic oxidation of carboxylic acid using different electrodes and electrolytic systems to synthesize fuels and chemicals.Also,various types of electrode catalysts,such as Pt-based catalysts,C-based catalysts,and other catalysts,are introduced in detail.Finally,the challenges and future trends of the(non-)Kolbe reaction of carboxylic acids are presented.This review found that platinum-based electrocatalysts proved to be the most promising catalysts at present.And in recent years,a variety of synthesis methods have been developed to synthesize small size and high-performance noble metal based amorphous catalysts.Another approach is to study catalysts without platinum electricity,such as Ru,Ir,Ti and carbon materials.The review is helpful in understanding and know the anodic materials and their application in(non-)Kolbe electrocatalytic decarboxylation of carboxylic acids for the readers.展开更多
Photosynthetic CO2 fixation is the ultimate source of organic carbon on earth and thus is essential for crop production and carbon sequestration, Ribulose-1,5-bis- phosphate carboxylase/oxygenase (Rubisco) catalyzes...Photosynthetic CO2 fixation is the ultimate source of organic carbon on earth and thus is essential for crop production and carbon sequestration, Ribulose-1,5-bis- phosphate carboxylase/oxygenase (Rubisco) catalyzes the first step of photosynthetic CO2 fixation. However, the extreme low carboxylation efficiency of Rubisco makes it the most attractive target for improving pho- tosynthetic efficiency. Extensive studies have focused on re-engineering a more efficient enzyme, but the effort has been impeded by the limited understanding of its structure-function relationships and the lack of an effi- cient selection system towards its activity. To address the unsuccessful molecular engineering of Rubisco, we developed an Escherichia coil-based activity-directed selection system which links the growth of host cell solely to the Rubisco activity therein. A Synechococcus sp. PCC7002 Rubisco mutant with E49V and D82G sub- stitutions in the small subunit was selected from a total of 15,000 mutants by one round of evolution. This mutant showed an 85% increase in specific carboxyla- tion activity and a 45% improvement in catalytic efficiency towards CO2. The small-subunit E49V mutation was speculated to influence holoenzyme catalysis through interaction with the large-subunit Q225. This interaction is conserved among various Rubisco from higher plants and Chlamydomonas reinhardtii. Knowledge of these might provide clues for engineering Rubisco from higher plants, with the potential of increasing the crop yield.展开更多
Carbon dioxide is a ubiquitous and inexpensive one-carbon source for chemical synthesis, and the efficient incorporation of CO2 into organic molecules is of widespread research interest both for economic and ecologica...Carbon dioxide is a ubiquitous and inexpensive one-carbon source for chemical synthesis, and the efficient incorporation of CO2 into organic molecules is of widespread research interest both for economic and ecological reasons. The methodologies to employ carbon dioxide as a single-carbon unit to construct molecules relevant for agrochemical and pharmaceutical research include many elegant approaches, including asymmetric transformations. Even though remarkable achievements have been made in the field of light-driven catalysis, especially photoredox catalysis, homogeneous light-driven catalytic carboxylation by employing CO2 as the key reagent has only become a subject of increasing attention in recent years. Therefore, this concise review will discuss the latest advances in this research area.展开更多
The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mi...The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mild reaction conditions,stoichiometric acceptor/donorless conditions(visible light photoredox catalysis)and chiral catalysts contributed to a rapid development of this intriguing research area capable of creating chemical diversity/complexity from readily available unsaturated hydrocarbons and CO2 as a C1-buinding block.The most recent developments in the field have been collected in the present review article and organized,based on the different sets ofπ-systems/intermediates/reactive partners employed(i.e.,nickelalactones,organo-halides)as well as synthetic strategies(i.e.,visible-light photo redox catalysis).展开更多
The increase in anthropogenic carbon dioxide(CO_(2))emissions has exacerbated the deterioration of the global environment,which should be controlled to achieve carbon neutrality.Central to the core goal of achieving c...The increase in anthropogenic carbon dioxide(CO_(2))emissions has exacerbated the deterioration of the global environment,which should be controlled to achieve carbon neutrality.Central to the core goal of achieving carbon neutrality is the utilization of CO_(2) under economic and sustainable conditions.Recently,the strong need for carbon neutrality has led to a proliferation of studies on the direct conversion of CO_(2) into carboxylic acids,which can effectively alleviate CO_(2) emissions and create high-value chemicals.The purpose of this review is to present the application prospects of carboxylic acids and the basic principles of CO_(2) conversion into carboxylic acids through photo-,electric-,and thermal catalysis.Special attention is focused on the regulation strategy of the activity of abundant catalysts at the molecular level,inspiring the preparation of high-performance catalysts.In addition,theoretical calculations,advanced technologies,and numerous typical examples are introduced to elaborate on the corresponding process and influencing factors of catalytic activity.Finally,challenges and prospects are provided for the future development of this field.It is hoped that this review will contribute to a deeper understanding of the conversion of CO_(2) into carboxylic acids and inspire more innovative breakthroughs.展开更多
Light-driven carbon dioxide(CO_(2))capture and utilization is one of the most fundamental reactions in Nature.Herein,we report the first visible-light-driven photocatalyst-free hydrocarboxylation of alkenes with CO_(2...Light-driven carbon dioxide(CO_(2))capture and utilization is one of the most fundamental reactions in Nature.Herein,we report the first visible-light-driven photocatalyst-free hydrocarboxylation of alkenes with CO_(2).Diverse acrylates and styrenes,including challenging tri-and tetrasubstituted ones,undergo anti-Markovnikov hydrocarboxylation with high selectivities to generate valuable succinic acid derivatives and 3-arylpropionic acids.In addition to the use of stoichiometric aryl thiols,the thiol catalysis is also developed,representing the first visible-lightdriven organocatalytic hydrocarboxylation of alkenes with CO_(2).The UV-vis measurements,NMR analyses,and computational investigations support the formation of a novel charge-transfer complex(CTC)between thiolate and acrylate/styrene.Further mechanistic studies and density functional theory(DFT)calculations indicate that both alkene and CO_(2)radical anions might be generated,illustrating the unusual selectivities and providing a novel strategy for CO_(2)utilization.展开更多
The E3 ubiquitin ligase,carboxyl terminus of heat shock protein 70(Hsp70)interacting protein(CHIP),also functions as a co-chaperone and plays a crucial role in the protein quality control system.In this study,we aimed...The E3 ubiquitin ligase,carboxyl terminus of heat shock protein 70(Hsp70)interacting protein(CHIP),also functions as a co-chaperone and plays a crucial role in the protein quality control system.In this study,we aimed to investigate the neuroprotective effect of overexpressed CHIP on Alzheimer’s disease.We used an adeno-associated virus vector that can cross the blood-brain barrier to mediate CHIP overexpression in APP/PS1 mouse brain.CHIP overexpression significantly ameliorated the performance of APP/PS1 mice in the Morris water maze and nest building tests,reduced amyloid-βplaques,and decreased the expression of both amyloid-βand phosphorylated tau.CHIP also alleviated the concentration of microglia and astrocytes around plaques.In APP/PS1 mice of a younger age,CHIP overexpression promoted an increase in ADAM10 expression and inhibitedβ-site APP cleaving enzyme 1,insulin degrading enzyme,and neprilysin expression.Levels of HSP70 and HSP40,which have functional relevance to CHIP,were also increased.Single nuclei transcriptome sequencing in the hippocampus of CHIP overexpressed mice showed that the lysosomal pathway and oligodendrocyte-related biological processes were up-regulated,which may also reflect a potential mechanism for the neuroprotective effect of CHIP.Our research shows that CHIP effectively reduces the behavior and pathological manifestations of APP/PS1 mice.Indeed,overexpression of CHIP could be a beneficial approach for the treatment of Alzheimer’s disease.展开更多
The recent Ir/Pd co-catalyzed photo carboxylation of aromatic halides with CO_(2) has shown high efficiency and excellent functional group tolerance for preparing aromatic carboxylic acids and esters.With the aid of d...The recent Ir/Pd co-catalyzed photo carboxylation of aromatic halides with CO_(2) has shown high efficiency and excellent functional group tolerance for preparing aromatic carboxylic acids and esters.With the aid of density functional theory(DFT)calculations,the carboxylation starts with two parallel steps,i.e.,oxidative addition of aromatic halides on Pd~0 and reductive quenching of the photocatalyst Ir(ppy)_(2)(dtbpy)~+with amine.Thereafter,a successive oxidation of Pd~Ⅱwith the amine radical(generated by the reaction of cationic radical amine and Cs_(2) CO_(3)and Ir~Ⅱspecies occurs to generate Pd~0,from which the carboxylation occurs easily via a coordination,Pd-C insertion step.The release of the carboxylate product then regenerates the catalyst.展开更多
Herein,we report a novel protocol for visible-light-driven alkylative carboxylation of alkenes with CO_(2) in the absence of external photocatalyst.Under the irradiation of visible light,a variety of 4-alkyl-1,4-dihyd...Herein,we report a novel protocol for visible-light-driven alkylative carboxylation of alkenes with CO_(2) in the absence of external photocatalyst.Under the irradiation of visible light,a variety of 4-alkyl-1,4-dihydropyridines(alkyl-DHPs)serve as not only alkyl radical precursors but also photoexcited reductants probably with the potential to reduce benzyl radicals.Several styrenes and acrylates are applicable in this reaction to give structurally diverse carboxylic acids in good to excellent yields.These reactions feature mild reaction conditions(1 atm of CO_(2),room temperature,visible light,photocatalyst-and transition metalfree),good functional group tolerance,easy scalability,as well as high regio-,and chemo-selectivity.Mechanistic investigations provide evidence that alkyl radical,benzyl radical and carbanion might be involved in this reaction,providing a novel strategy for CO_(2) utilization.展开更多
基金received from the National Natural Science Foundation of China(No.22278305)National Key R&D Program of China(2022YFB4101900)。
文摘Electrocarboxylation of carbon dioxide(CO_(2))using organic substrates has emerged as a promising method for the sustainable synthesis of value-added carboxylic acids due to its renewable energy source and mild reaction conditions.The reactivity and product selectivity of electrocarboxylation are highly dependent on the cathodic behavior,involving a sequence of electron transfers and chemical reactions.Hence,it is necessary to understand the cathodic reaction mechanisms for optimizing reaction performance and product distribution.In this work,a review of recent advancements in the electrocarboxylation of CO_(2)with organic substrates based on different cathodic reaction pathways is presented to provide a reference for the development of novel methodologies of CO_(2)electrocarboxylation.Herein,cathodic reactions are particularly classified into two categories based on the initial electron carriers(i.e.,CO_(2)radical anion and substrate radical anion).Furthermore,three cathodic pathways(ENE(N),ENED,and EDEN)of substrate radical anion-induced electrocarboxylation are discussed,which differ in their electron transfer sequence,substrate dissociation,and nucleophilic reaction,to highlight their implications on reactivity and product selectivity.
文摘Carboxylation of aromatics by CO2 to generate corresponding carboxylic acids is recently providing a novel approach to utilize the green gas CO2, in which the activation of CO2 is the key procedure. Among the many catalytic systems employed in the carboxylation, the concept of “Frustrated Lewis Pairs” (FLPs) was scarcely mentioned, which perform excellently in activating small molecules like CO2. The FLPs are combinations of Lewis acids and Lewis bases which failed to form adducts due to their bulky steric congestion. In this paper, we first attempted various Si/Al Based FLPs to catalyze the carboxylation of aromatics through the activation of CO2, and a good yield of 62% - 97% was obtained. The reaction mechanism was proposed, involving the activation of CO2 mainly contributed by AlCl3 in cooperation with organosilane, forming an intermediate consisting of CO2, AlCl3, and R4Si, as well as the subsequent electrophilic attack to aromatics, thus to promote the carboxylation reaction.
文摘A feasible synthesis route is developed for achieving the direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten state.The effects of reaction factors on the carboxylate yield are investigated in the preliminary screening experiments,and the phase behavior analysis of the reaction medium is detected through the thermal characterization analysis of insitu high temperature X-ray diffraction measurement(in-situ XRD).The application of response surface methodology(RSM)based on the Box-Behnken design(BBD)is conducted to investigate the effect of the reaction parameters,such as reaction temperatu re,carbonate proportion,CO_(2) pressure and thiophene amount,on the product yield.The regressed second-order polynomial model equation well correlates all the independent variables.The analysis of variance(ANOVA)results reveal that the quadratic effect of reaction temperature is the most effective parameter in this carboxylation reaction owing to it’s the highest contribution to the sum of square(30.18%).The optimum reaction conditions for maximum product yield are the reaction temperature of 287℃,carbonate proportion of 32.20%,CO_(2) pressure of 1.0MPa and thiophene amount of 9.35 mmol.Operating under these selected experimental conditions,a high product yield(50.98%)can be achieved.
文摘A feasible synthesis route is devised for realizing direct carboxylation of thiophene and CO_(2) in a relatively mild solvent-free carboxylate-assisted carbonate(semi)molten medium.The effects of reaction factors on product yield are investigated,and the phase behavior analysis of the reaction medium is detected through the thermal characterization techniques.Product yield varies with the alternative carboxylate co-salts,which is attributed to the difference in deprotonation capacity caused by the base effect within the system.Besides,the detailed mechanism of this carbonate-promoted carboxylation reaction is studied,including two consecutive steps of the formation of carbanion through breaking the C-H bond(s)via the carbonate and the nucleophile attacking the weak electrophile CO_(2) to form C-C bond(s).The activation energy barrier in C-H activation step is higher than the following CO_(2) insertion step whether for the formation of the mono-and/or di-carboxylate,which is in good agreement with that of kinetic isotope effect(KIE)experiments,indicating that the C-H deprotonation is slow and the forming presumed carbanion reacts rapidly with CO_(2).Both the activation energy barriers in deprotonation steps are the minimal for the cesium cluster system since there have the weak the cesium Cs-heteroatom S(thiophene)and Cs-the broken proton interactions compared to the K2CO3 system,which is likely to enhance the acidity of C-H bond,lowering the C-H activation barrier.Besides,these mechanistic insights are further assessed by investigating base and C-H substrate effects via replacing Cs2CO3 with K2CO3 and furoate(la)with thiophene monocarboxylate(1b)or benzoate(1c).
文摘Manganese(Ⅲ) meso-tetraphenylporphyrin acetate [Mn(TPP)OAc] served as an effective catalyst for the oxidative decarboxylation of carboxylic acids with (diacetoxyiodo)benzene [PhI(OAc)2] in CH2CI2-H2O(95:5, volume ratio). The aryl substituted acetic acids are more reactive than the less electron rich linear carboxylic acids in the presence of catalyst Mn(TPP)OAc. In the former case, the formation of carbonyl products was complete within just a few minutes with 〉97% selectivities, and no further oxidation of the produced aldehydes was achieved under these catalytic conditions. This method provides a benign procedure owing to the utilization of low toxic(diacetoxyiodo) benzene, biologically relevant manganese porphyrins, and carboxylic acids.
文摘A direct regioselective preparation of 2-hydroxynaphthalene-6-carboxylic acid, a useful industrial intermediate of aro-matic polyester from 2-naphthol was conducted by use of excess amount of K2CO3 (10-fold molar to 2-naphthol) under supercritical CO2 at 10 MPa and 473 K. The obtained yield under this condition was ca. 20 mol% to 2-naphthol. The further investigations may provide an alternative process to the conventional Kolbe-Schmitt reaction, because of no use of strong alkali and recoverability of K2CO3. Theoretical explanation about the regioselectivity was achieved by means of DFT calculations.
文摘The mechanism and the final outcome of the Knoevenagel-Doebner reaction are discussed. The condensation reaction between different hydroxy-substituted aromatic aldehydes and malonic acid is performed using piperidine as organocatalyst. The key role of the catalyst is clearly pointed out during the decarboxylation of ferulic acid, without the use of a strong decarboxylating agent, leading to a 4-vinylphenol derivative. Based on the results obtained, the studied pathway may be important in the understanding of vinylphenol production during malting and brewing of wheat and barley grains. Finally, changing the solvent of the reaction from pyridine to water in the Knoevenagel-Doebner reaction of 4-hydroxybenzaldehydes, dimerization of resulting styrene derivatives is observed. These results can be of interest also in the field of food chemistry, since cinnamic acids are frequently found in fruits and vegetables used for human consumption.
基金partly supported by Russian Academy of Science Project No. V.46.4.4Part of work related to metal oxides was supported by RFBR grant 15-03-09329
文摘The combination of a low cost source of Biofine's levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable compounds for transportation sector. The present review illustrates the development of different approaches to one–pot synthesis of fuel-like alkanes from lignocellulose derived carboxylic acids where particular focus is given to valeric acid consecutive decarboxylative coupling(ketonization) and ketone hydrodeoxygenation in a single reactor over one catalyst bed. The key factors that influence the catalytic performance on both ketonization and hydrodeoxygenation steps as well as their cross-influence will be clarified to provide insights for the design of more efficient catalysts for the one-pot transformation. Valeric acid is considered as a potential acid source from viewpoint of cost effectiveness and feasibility of such transformation with reasonable alkane yield. The both reaction mechanisms and kinetics will also be discussed to understand deeply how the selective C–C coupling and following C=O hydrogenation can be achieved.
基金supported by the National Natural Science Foundation of China(22379054)and start-up funding from Jiangnan University.
文摘Recently,significant research has been conducted on the conversion of carbon dioxide(CO_(2))into value-added chemicals.With the decreasing cost of clean electricity,electrochemical methods have emerged as potential approaches for converting and fixing CO_(2).Organic electrochemical synthesis is a promising method for utilizing CO_(2)because it transforms CO_(2)into higher-value chemicals.This review introduces the research aspects of CO_(2)conversion and the mechanisms of CO_(2)organic electrocarboxylation reactions.Recent progress in electrocarboxylation with CO_(2)is discussed,considering organic substrates and cathode types under different reaction mechanisms.Finally,the challenges and prospects in this field are highlighted with the aim of further promoting the fundamental understanding of CO_(2)organic electrocarboxylation.
基金Financial support from the National Natural Science Foundation of China(No.21901041)the Fuzhou University(No.0041/511095)。
文摘As an attractive C1 synthon,carbon dioxide(CO_(2))has been extensively used in organic synthesis to produce carboxylic acids.In this research,stereoselective electrochemical carboxylation ofα,β-unsaturated sulfones has been developed under transition-metal-free conditions.All the cinnamic acids and the derivatives are obtained selectively in the E-configuration.Besides,arylpropiolates also can be produced from alkynyl sulfones.
基金supported by the National Natural Science Foundation of China(22225106,21822108,21822303)the Sichuan Science and Technology Program(20CXTD0112)+2 种基金the Central Government Funds of Guiding Local Scientific and Technological Development for Sichuan Province(2021ZYD0063)the Fundamental Research Funds from Sichuan University(2020SCUNL102)the Fundamental Research Funds for the Central Universities。
文摘Difunctionalizing carboxylation of alkynes with CO_(2)is a sustainable and important strategy to generate valuable acrylate derivatives from both readily available starting materials.Such protocols,however,always suffer from the use of excess metallic reagents and transition metal residue.Herein,we report the first thio-carboxylation of alkynes with thiophenols and CO_(2),which is a visible-light-driven and transition metal-free process.In contrast to previous carboxylations of alkynes via two-electron activation of CO_(2),mechanistic and computational investigations suggest that the single-electron activation of CO_(2)is involved in the thio-carboxylation,rendering uniqueβ-carboxylation.The following cyclizing acylation affords important thiochromones efficiently.Moreover,the one-pot method features mild reaction conditions(room temperature,1 atmosphere of CO_(2)),high chemo-and regio-selectivity,easy scalability and facile derivatization of products to bioactive compounds.
基金the financial support from Shanghai Pujiang Program(20PJ1404800)The National Natural Science Foundation of China(No.21671139)Shanghai Science and Technology Development Fund(20DZ2250700).
文摘Biomass,as the exclusive and abundant organic resources,is considered to be the promising renewable resource.Carboxylic acids are one of the many compounds that can be obtained from raw biomass.Decarboxylation of carboxylic acids into fuels and chemicals via electrochemical method at mild reaction condition has been studied for many years.The(non-)Kolbe reaction,one of the oldest organic electrochemical reactions,is the decarboxylation of carboxylic acids to produce alkanes,alcohols,esters,etc.And electrode materials influence the production of electrocatalytic decarboxylation products from carboxylic acids.Therefore,this work mainly reviews the recent advances in applications of anodic materials for(non-)Kolbe electrocatalytic decarboxylation of carboxylic acids.It discusses the reaction mechanism of(non-)Kolbe electrolytic reaction,and the electrocatalytic oxidation of carboxylic acid using different electrodes and electrolytic systems to synthesize fuels and chemicals.Also,various types of electrode catalysts,such as Pt-based catalysts,C-based catalysts,and other catalysts,are introduced in detail.Finally,the challenges and future trends of the(non-)Kolbe reaction of carboxylic acids are presented.This review found that platinum-based electrocatalysts proved to be the most promising catalysts at present.And in recent years,a variety of synthesis methods have been developed to synthesize small size and high-performance noble metal based amorphous catalysts.Another approach is to study catalysts without platinum electricity,such as Ru,Ir,Ti and carbon materials.The review is helpful in understanding and know the anodic materials and their application in(non-)Kolbe electrocatalytic decarboxylation of carboxylic acids for the readers.
文摘Photosynthetic CO2 fixation is the ultimate source of organic carbon on earth and thus is essential for crop production and carbon sequestration, Ribulose-1,5-bis- phosphate carboxylase/oxygenase (Rubisco) catalyzes the first step of photosynthetic CO2 fixation. However, the extreme low carboxylation efficiency of Rubisco makes it the most attractive target for improving pho- tosynthetic efficiency. Extensive studies have focused on re-engineering a more efficient enzyme, but the effort has been impeded by the limited understanding of its structure-function relationships and the lack of an effi- cient selection system towards its activity. To address the unsuccessful molecular engineering of Rubisco, we developed an Escherichia coil-based activity-directed selection system which links the growth of host cell solely to the Rubisco activity therein. A Synechococcus sp. PCC7002 Rubisco mutant with E49V and D82G sub- stitutions in the small subunit was selected from a total of 15,000 mutants by one round of evolution. This mutant showed an 85% increase in specific carboxyla- tion activity and a 45% improvement in catalytic efficiency towards CO2. The small-subunit E49V mutation was speculated to influence holoenzyme catalysis through interaction with the large-subunit Q225. This interaction is conserved among various Rubisco from higher plants and Chlamydomonas reinhardtii. Knowledge of these might provide clues for engineering Rubisco from higher plants, with the potential of increasing the crop yield.
基金We thank the National Natural Science Foundation of China (Nos. 21602052 and 21702151) for financial support.
文摘Carbon dioxide is a ubiquitous and inexpensive one-carbon source for chemical synthesis, and the efficient incorporation of CO2 into organic molecules is of widespread research interest both for economic and ecological reasons. The methodologies to employ carbon dioxide as a single-carbon unit to construct molecules relevant for agrochemical and pharmaceutical research include many elegant approaches, including asymmetric transformations. Even though remarkable achievements have been made in the field of light-driven catalysis, especially photoredox catalysis, homogeneous light-driven catalytic carboxylation by employing CO2 as the key reagent has only become a subject of increasing attention in recent years. Therefore, this concise review will discuss the latest advances in this research area.
基金Financial support by the National Key Research and Development Program of China(Grants 2017YFA0204503 and 2017YFA0207800)the National Natural Science Foundation of China(Grants 51903187,21734006 and 21975178)the China Postdoctoral Science Foundation(No.2020M670642)is gratefully acknowledged.
文摘The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mild reaction conditions,stoichiometric acceptor/donorless conditions(visible light photoredox catalysis)and chiral catalysts contributed to a rapid development of this intriguing research area capable of creating chemical diversity/complexity from readily available unsaturated hydrocarbons and CO2 as a C1-buinding block.The most recent developments in the field have been collected in the present review article and organized,based on the different sets ofπ-systems/intermediates/reactive partners employed(i.e.,nickelalactones,organo-halides)as well as synthetic strategies(i.e.,visible-light photo redox catalysis).
基金financial support from the King Abdullah University of Science and Technology(KAUST).
文摘The increase in anthropogenic carbon dioxide(CO_(2))emissions has exacerbated the deterioration of the global environment,which should be controlled to achieve carbon neutrality.Central to the core goal of achieving carbon neutrality is the utilization of CO_(2) under economic and sustainable conditions.Recently,the strong need for carbon neutrality has led to a proliferation of studies on the direct conversion of CO_(2) into carboxylic acids,which can effectively alleviate CO_(2) emissions and create high-value chemicals.The purpose of this review is to present the application prospects of carboxylic acids and the basic principles of CO_(2) conversion into carboxylic acids through photo-,electric-,and thermal catalysis.Special attention is focused on the regulation strategy of the activity of abundant catalysts at the molecular level,inspiring the preparation of high-performance catalysts.In addition,theoretical calculations,advanced technologies,and numerous typical examples are introduced to elaborate on the corresponding process and influencing factors of catalytic activity.Finally,challenges and prospects are provided for the future development of this field.It is hoped that this review will contribute to a deeper understanding of the conversion of CO_(2) into carboxylic acids and inspire more innovative breakthroughs.
基金Financial support was provided by the the National Natural Science Foundation of China(nos.21822108,21822303,21801176,21772129,and 21772020)the Fok Ying Tung Education Foundation(no.161013)+1 种基金Sichuan Science and Technology Program(nos.2019YJ0379 and 20CXTD0112)the Fundamental Research Funds for the Central Universities.
文摘Light-driven carbon dioxide(CO_(2))capture and utilization is one of the most fundamental reactions in Nature.Herein,we report the first visible-light-driven photocatalyst-free hydrocarboxylation of alkenes with CO_(2).Diverse acrylates and styrenes,including challenging tri-and tetrasubstituted ones,undergo anti-Markovnikov hydrocarboxylation with high selectivities to generate valuable succinic acid derivatives and 3-arylpropionic acids.In addition to the use of stoichiometric aryl thiols,the thiol catalysis is also developed,representing the first visible-lightdriven organocatalytic hydrocarboxylation of alkenes with CO_(2).The UV-vis measurements,NMR analyses,and computational investigations support the formation of a novel charge-transfer complex(CTC)between thiolate and acrylate/styrene.Further mechanistic studies and density functional theory(DFT)calculations indicate that both alkene and CO_(2)radical anions might be generated,illustrating the unusual selectivities and providing a novel strategy for CO_(2)utilization.
基金supported by the National Natural Science Foundation of China,Nos.91849115 and U1904207(to YX),81974211 and 82171247(to CS)Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences,No.2020-PT310-01(to YX).
文摘The E3 ubiquitin ligase,carboxyl terminus of heat shock protein 70(Hsp70)interacting protein(CHIP),also functions as a co-chaperone and plays a crucial role in the protein quality control system.In this study,we aimed to investigate the neuroprotective effect of overexpressed CHIP on Alzheimer’s disease.We used an adeno-associated virus vector that can cross the blood-brain barrier to mediate CHIP overexpression in APP/PS1 mouse brain.CHIP overexpression significantly ameliorated the performance of APP/PS1 mice in the Morris water maze and nest building tests,reduced amyloid-βplaques,and decreased the expression of both amyloid-βand phosphorylated tau.CHIP also alleviated the concentration of microglia and astrocytes around plaques.In APP/PS1 mice of a younger age,CHIP overexpression promoted an increase in ADAM10 expression and inhibitedβ-site APP cleaving enzyme 1,insulin degrading enzyme,and neprilysin expression.Levels of HSP70 and HSP40,which have functional relevance to CHIP,were also increased.Single nuclei transcriptome sequencing in the hippocampus of CHIP overexpressed mice showed that the lysosomal pathway and oligodendrocyte-related biological processes were up-regulated,which may also reflect a potential mechanism for the neuroprotective effect of CHIP.Our research shows that CHIP effectively reduces the behavior and pathological manifestations of APP/PS1 mice.Indeed,overexpression of CHIP could be a beneficial approach for the treatment of Alzheimer’s disease.
基金the financial support from the National Natural Science Foundation of China(Nos.21672001,51961135104)the technical support of high-performance computing platform of Anhui University。
文摘The recent Ir/Pd co-catalyzed photo carboxylation of aromatic halides with CO_(2) has shown high efficiency and excellent functional group tolerance for preparing aromatic carboxylic acids and esters.With the aid of density functional theory(DFT)calculations,the carboxylation starts with two parallel steps,i.e.,oxidative addition of aromatic halides on Pd~0 and reductive quenching of the photocatalyst Ir(ppy)_(2)(dtbpy)~+with amine.Thereafter,a successive oxidation of Pd~Ⅱwith the amine radical(generated by the reaction of cationic radical amine and Cs_(2) CO_(3)and Ir~Ⅱspecies occurs to generate Pd~0,from which the carboxylation occurs easily via a coordination,Pd-C insertion step.The release of the carboxylate product then regenerates the catalyst.
基金supported by the National Natural Science Foundation of China(21822108,21772129)the Fok Ying Tung Education Foundation(161013)+1 种基金Sichuan Science and Technology Program(20CXTD0112)Fundamental Research Funds for the Central Universities。
文摘Herein,we report a novel protocol for visible-light-driven alkylative carboxylation of alkenes with CO_(2) in the absence of external photocatalyst.Under the irradiation of visible light,a variety of 4-alkyl-1,4-dihydropyridines(alkyl-DHPs)serve as not only alkyl radical precursors but also photoexcited reductants probably with the potential to reduce benzyl radicals.Several styrenes and acrylates are applicable in this reaction to give structurally diverse carboxylic acids in good to excellent yields.These reactions feature mild reaction conditions(1 atm of CO_(2),room temperature,visible light,photocatalyst-and transition metalfree),good functional group tolerance,easy scalability,as well as high regio-,and chemo-selectivity.Mechanistic investigations provide evidence that alkyl radical,benzyl radical and carbanion might be involved in this reaction,providing a novel strategy for CO_(2) utilization.