The ring-opening alternating copolymerization(ROAC)of 3,4-dihydrocoumarin(DHC)/epoxides has been successfully developed using an imidazolium salt of 1-ethyl-3-methylimidazolium chloride(EMIMCl)as a catalyst.The result...The ring-opening alternating copolymerization(ROAC)of 3,4-dihydrocoumarin(DHC)/epoxides has been successfully developed using an imidazolium salt of 1-ethyl-3-methylimidazolium chloride(EMIMCl)as a catalyst.The resulting copolymer has a molecular weight of 13.7kg·mol^(-1),a narrow molecular weight distribution of 1.03 and a strictly alternating structure.The MALDI-TOF MS characterization and DFT calculations including electrostatic potential(ESP),hydrogen-atom abstraction(HAA),independent gradient model based on hirshfeld partition(IGMH)and atoms-in-molecules(AIM)analysis were used to investigate the metal-free catalytic process.The synergistic effect of anions and cations of EMIMCl for ROAC of DHC and epoxides was demonstrated.This study provides a metal-free catalytic system for the facile synthesis of alternating polyesters from DHC.展开更多
Polyhydroxyalkanoate(PHA),a well-known biodegradable polymer,featuresβ-lactones as its monomers,which can be selectively synthesized through ring-expansion carbonylation of epoxides using well-defined[Lewis acid]^(+)...Polyhydroxyalkanoate(PHA),a well-known biodegradable polymer,featuresβ-lactones as its monomers,which can be selectively synthesized through ring-expansion carbonylation of epoxides using well-defined[Lewis acid]^(+)[Co(CO)_(4)]^(-)catalysts.However,the decomposition of[Co(CO)_(4)]^(-)species at temperatures exceeding 80℃presents a hurdle for the development of commercially viable processes under high-temperature reaction conditions to reduce reaction time.Drawing insights from stable{(acyl)Co(CO)n}intermediates involved in historical HCo(CO)_(4)-catalyzed hydroformylation processes,we sought to the high-temperature catalytic activity of epoxide ring-expansion carbonylation.The developed catalyst system,[(acetyl)Co(CO)_(2)dppp]and[(TPP)CrCl],exhibited exceptional catalytic performance with an unprecedented initial turnover frequency of 4700 h^(-1)at 100℃and a turnover numbers of 93000.Notably,the catalyst displayed outstanding stability,operating at 80℃for 168 h while selectively generatingβ-lactones.展开更多
Herein, we report the first visible-light photoredox-catalyzed carboxylation of aryl epoxides with CO_(2)to synthesize hydroxy acid derivatives. A variety of valuable β-, γ-, δ-, ε–hydroxy acid derivatives are ob...Herein, we report the first visible-light photoredox-catalyzed carboxylation of aryl epoxides with CO_(2)to synthesize hydroxy acid derivatives. A variety of valuable β-, γ-, δ-, ε–hydroxy acid derivatives are obtained in moderate to high yields under mild conditions. This protocol shows noteworthy functionalgroup compatibility, high chemo-and regioselectivities under transition-metal-free conditions with an inexpensive organo-dye as photosensitizer. Mechanistic studies indicate that the benzylic carbanion is generated as an intermediate via the sequential single electron transfer(SSET) process.展开更多
The aim of ＂green chemistry＂ and ＂atom economy＂ is to utilize carbon dioxide and replace harmful reactants such as CO and phosgene for the production of cyclic carbonates. In this paper, metal-free catalysts inclu...The aim of ＂green chemistry＂ and ＂atom economy＂ is to utilize carbon dioxide and replace harmful reactants such as CO and phosgene for the production of cyclic carbonates. In this paper, metal-free catalysts including organic bases, ionic liquids, supported catalysts, organic copolymers and carbon materials for the synthesis of cyclic carbonates by the cycloaddition of carbon dioxide to epoxides are reviewed. Recent advances in the design of the catalysts and the understanding of the reaction mechanism are summarized and discussed. The synergistic effects of organic bases and hydrogen bond donors, organic bases and nucleophilic anions, hydrogen bond donors and nucleophilic anions and active components and supports are highlighted. The challenge is to develop metal-free catalysts suitable for carbon dioxide capture and fixation. The ultimate goal is to synthesize cyclic carbonates in a flow reactor directly using carbon dioxide from industrial flue gas at ambient temperature and atmospheric pressure. By using synergetic effects, a multi-functional approach can meet the design strategy of metal-free catalysts for carbon dioxide adsorption and activation as well as epoxide ring opening.展开更多
Three new cyclohexene epoxides,polysyphoside A,B and C,along with a known compound crotepoxide(4),were isolated from Piper polysyphorum C.DC.Based on spectroscopic analysis,their structures were established as 1-benzo...Three new cyclohexene epoxides,polysyphoside A,B and C,along with a known compound crotepoxide(4),were isolated from Piper polysyphorum C.DC.Based on spectroscopic analysis,their structures were established as 1-benzoyloxymethylene-2-hydroxy-3-benzoyloxy-1,6- epoxycyclohex-4-ene(1),1-benzoyloxymethylene-2-hydroxy-5-benzoyloxy-1,6-epoxycyclohex-3-ene (2)and 2-hydroxy-3-benzoyloxymethylene-5-benzoyloxy-1,6-epoxycyclohex-3-ene(3),respectively.It was the first time that(1),(2)and(3)had been isolated from a natural source.展开更多
This report presents a detailed density functional theory （DFT） study on the difference in regioselectivity for the copolymerization reactions of styrene oxide versus propylene oxide with CO2 utilizing binary （sale...This report presents a detailed density functional theory （DFT） study on the difference in regioselectivity for the copolymerization reactions of styrene oxide versus propylene oxide with CO2 utilizing binary （salen）cobalt（III） catalyst systems. This study focuses on the discrepancy of regioselective ring-opening of two terminal epoxides during the copolymerization with CO2. It was found that the nucleophilic ring-opening of styrene oxide occurred predominantly at the methine C a--O bond due to the election delocalization of phenyl group to stabilize the transition state for the methine C--O bond cleavage.展开更多
[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane was synthesized,using tert-butyldimethylsilane(TBDMS)and 1,2-epoxy-4-vinylcyclohexane(EVC)as the main raw materials and tris(triphenylphosphine)chlororhodium(I)[...[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane was synthesized,using tert-butyldimethylsilane(TBDMS)and 1,2-epoxy-4-vinylcyclohexane(EVC)as the main raw materials and tris(triphenylphosphine)chlororhodium(I)[RhCl(Ph3P)3]as the catalyst.[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane is a novel kind of silicon-containing epoxide.The factors affecting the reaction yield,such as catalyst use,reaction time and reaction temperature,were investigated,and the synthesized product was characterized and analyzed by FT-IR and 1H-NMR.A series of amine-curing resins were prepared with[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane,bisphenol A epoxy resin(E-51)and modified amine(593 amine).The mechanical properties of cured splines with the different proportions of amine-curing resins were tested.When the content of 593 amine was 20%,the content of E-51 was 75%and the amount of[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane was 5%,the mechanical properties of the cured splines were the best with the tensile strength being 23.3 MPa,the elongation at break being 7.8%,and the Young's modulus being 421.3 MPa.展开更多
In the context of peaking carbon dioxide emissions and carbon neutrality,development of feasible methods for converting CO_(2)into high value-added chemicals stands out as a hot subject.In this study,P[D+COO^(−)][Br^(...In the context of peaking carbon dioxide emissions and carbon neutrality,development of feasible methods for converting CO_(2)into high value-added chemicals stands out as a hot subject.In this study,P[D+COO^(−)][Br^(−)][DBUH^(+)],a series of novel heterogeneous dual-ionic poly(ionic liquid)s(PILs)were synthesized readily from 2-(dimethylamino)ethyl methacrylate(DMAEMA),bromo-substituted aliphatic acids,organic bases and divinylbenzene(DVB).The structures,compositions and morphologies were characterized or determined by nuclear magnetic resonance(NMR),thermal gravimetric analysis(TGA),infrared spectroscopy(IR),scanning electron microscopes(SEM),and Brunauer-Emmett-Teller analysis(BET),etc.Application of the P[D+COO^(−)][Br^(−)][DBUH^(+)]series as catalysts in converting CO_(2)into cyclic carbonates showed that P[D+COO^(−)][Br^(−)][DBUH^(+)]-2/1/0.6was able to catalyze epiclorohydrin-CO_(2)cycloaddition the most efficiently.This afforded chloropropylene carbonate(CPC)in 98.4%yield with≥99%selectivity in 24 hr under solvent-and additive-free conditions at atmospheric pressure.Reusability experiments showed that recycling of the catalyst 6 times only resulted in a slight decline in the catalytic performance.In addition,it could be used for the synthesis of a variety of differently substituted cyclic carbonates in good to excellent yields.Finally,key catalytic active sites were probed,and a reasonable mechanism was proposed accordingly.In summary,this work poses an efficient strategy for heterogenization of dual-ionic PILs and provides amild and environmentally benign approach to the fixation and utilization of carbon dioxide.展开更多
Selective oxidation of olefin to epoxides is an important reaction in industry,however,developing heterogeneous catalysts to achieve the effective catalysis for this reaction under O_(2)atmosphere at room temperature ...Selective oxidation of olefin to epoxides is an important reaction in industry,however,developing heterogeneous catalysts to achieve the effective catalysis for this reaction under O_(2)atmosphere at room temperature is challenging but highly desired.In this work,two novel 2D cobalt metal-organic complexes,namely[Co(L)(5-HIP)]·2H_(2)O(Co-MOC-1)and[Co(L)(BTEC)_(0.5)]·H_(2)O(Co-MOC-2)(L=(E)-4,4-(ethene-1,2-diyl))bis(N-(pyridin-3-yl)benzamide;5-H_(2)HIP=5-hydroxyisophthalic acid;H4BTEC=pyromellitic acid)were designed and synthesized through hydrothermal method,which exhibited different metal coordination modes(4-coordinate and 5-coordinate,respectively)and 2D layer structures directed by different carboxylates co-ligands.Two Co-MOCs can serve as heterogeneous catalysts for the selective oxidation of olefins to epoxides at room temperature using O_(2)as oxidant.Furthermore,a higher catalysis activity of Co-MOC-1 than Co-MOC-2(96.7%vs.90.2%yield of 1,2-epoxycyclooctane)was observed,which may be attributed to the coordination unsaturated Co centers,the less coordination number and larger interlayer spacing of Co-MOC-1.展开更多
Resin plugging agents play a pivotal role in addressing casing damage in oil and gas fields.However,the widespread use of epoxy resin is constrained by its high cost and non-renewable origin,while plant-based resins o...Resin plugging agents play a pivotal role in addressing casing damage in oil and gas fields.However,the widespread use of epoxy resin is constrained by its high cost and non-renewable origin,while plant-based resins often suffer from inadequate mechanical properties,which limit their effectiveness in such applications.This study introduces BEOPA,an innovative,renewable,high-strength resin plugging agent derived from epoxidized soybean oil(ESO)and enhanced with bisphenol A-type benzoxazine(BZ).In this study,the synthesis process,reactionmechanism,and application performance of this novelmaterial are systematically presented,explored and optimized.It is shown that the optimal formulation of BEOPA includes 41.4 wt%ESO,24.8 wt%BZ,24.8 wt%methylhexahydrophthalic anhydride(MHHPA),8.2 wt%styrene(ST),and 0.8 wt%N,N-dimethylbenzylamine(BDMA),yielding an impressive compressive strength of 93.7 MPa.The integration of ESO and BZ creates an intricate and robust double crosslinking network,significantly enhancing material strength and durability.BEOPA exhibits a tunable curing time,ranging from 0.5 to 15 h,with viscosities below 300 mPa⋅s at 25℃and 75mPa⋅s at 50℃.Furthermore,it demonstrates exceptional thermal stability within the 100℃-150℃range,even in environments with mineral salt concentrations as high as 43,330 mg/L.Remarkably,BEOPA achieves superior plugging performance,sustaining breakthrough pressures exceeding 29.7 MPa in 1 mm crack cores.展开更多
Objective:Soluble epoxide hydrolase(sEH)emerges as a target of interest for inflammatory diseases.Piperine is a natural amide alkaloid from Piper nigrum and displays an inhibitory effect toward sEH,its chemical struct...Objective:Soluble epoxide hydrolase(sEH)emerges as a target of interest for inflammatory diseases.Piperine is a natural amide alkaloid from Piper nigrum and displays an inhibitory effect toward sEH,its chemical structural transformation was carried out in order to obtain a library of sEH inhibitors based on its skeleton.Methods:Structural transformation of piperine was carried out by chemical methods,and piperine derivatives were assayed for their sEH potentials.A mouse acute lung injury model was constructed by lipopolysaccharide(LPS).Hematoxylin and eosin(H&E)staining,immunofluorescence staining,Western Blot,and enzyme-linked immunosorbent assay were used for investigating the protective potential of sEH inhibitor 11h.Results:Piperine derivatives 11e,11h,11j,and 11o showed inhibitory potentials toward sEH with values of half maximal inhibitory concentration(IC50)from 20 to 70 nM.Compound 11h attenuated the pathological course of LPS-mediated acute lung injury(ALI)in vivo.Furthermore,levels of cytokines tumor necrosis factor alpha(TNF-α),interleukin 6(IL-6),myeloperoxidase(MPO),and lactate dehydrogenase(LDH)were decreased after administration of 11h.The LPS-mediated inflammation and redox unbalance,including expressions of cyclooxygenase-2(COX-2),heme oxygenase-1(HO-1),intercellular cell adhesion molecule-1(ICAM-1),vascular cell adhesion molecule-1(VCAM-1),p-p65/p65,glutamate-cysteine ligase modifier subunit(GCLM),and nuclear factor erythroid-2-related factor 2(Nrf2),were ameliorated through nuclear factor kappa B(NF-κB)and Nrf2 pathways via enhancing levels of epoxyeicosatrienoic acids(EETs)in LPS-exposed ALI mice after compound 11h treatment.Molecular docking demonstrated that the aromatic unsaturated group of 11h occupied a hydrophobic pocket and its urea group formed three hydrogen bonds with Asp333,Tyr381,and Tyr465,which stabilized the active conformation of the ligand.Conclusions:These findings demonstrated that compound 11h may serve as a lead compound for developing sEH inhibitors and treating inflammation related to diseases,such as ALI.展开更多
Studies on the use of renewable materials for various applications,including polymers,have gained momentum due to global climate change and the push towards a circular economy.In this study,polymer resins were develop...Studies on the use of renewable materials for various applications,including polymers,have gained momentum due to global climate change and the push towards a circular economy.In this study,polymer resins were developed through Michael 1,4-addition.The precursors were synthesized from tall oil-based acetoacetates derived from epoxidized tall oil fatty acids or their methyl esters.Two different epoxidation methods were employed:enzymatic epoxidation of tall oil fatty acids and ion-exchange resin epoxidation of tall oil fatty acid methyl esters.Following oxirane opening and transesterification with trimethylolpropane,further esterification or transesterification was carried out to obtain the acetoacetates.These synthesized acetoacetates were then reacted with acrylates of various functionalities to obtain polymer resins with differing degrees of crosslinking.The developed polymer resins were characterized using differential scanning calorimetry,dynamic mechanical analysis,and thermogravimetric analysis.The results indicated that the glass transition temperature and storage modulus of the polymer resins were significantly influenced by both the functionality of the acrylates used and the epoxidation technique employed.Higher acrylate functionality resulted in increased stiffness,while enzymatic epoxidation enhanced the polymer’s mechanical properties,nearly doubling the storage modulus,achieving approximately 470 MPa,compared to the ion-exchange resin technique.Therefore,selecting the appropriate acrylate functionality and epoxidation method could tailor the mechanical properties of the polymer resins.展开更多
In this study,epoxidized soybean oil(ESO)and ricinoleic acid(RA)were used to synthesize polyol esters,designated ESO-RA(ER)resin.The esters were further crosslinked with 4,4-diphenylmethane diisocyanate(PMDI)to create...In this study,epoxidized soybean oil(ESO)and ricinoleic acid(RA)were used to synthesize polyol esters,designated ESO-RA(ER)resin.The esters were further crosslinked with 4,4-diphenylmethane diisocyanate(PMDI)to create a biodegradable flame-retardant thermoset foam,referred to as ESO-RA-PMDI(ERP)foam,using water as a foaming agent.Additionally,flame retardants such as triethyl phosphate(TEP)and expanded graphite(EG)have been combined for foam preparation without the need for catalysts or foaming agents.The study findings showed that the incorporation of TEP and EG diminished the pulverization ratio while augmenting the compressive strength and shore hardness.Furthermore,the ERP foam exhibited exceptional flame retardant characteristics,as evidenced by a reported limiting oxygen index(LOI)value of 30.6vol%.A peak heat release rate of 97.12 kW/m^(2)was reported during the fire test.Significantly,a low peak smoke production rate(pSPR)of 0.026m^(2)/s and a total smoke production(TSP)of 0.62 m^(2)were achieved.In addition,ERP foam exhibited exceptional ultraviolet(UV)resistance,thermal insulation,and biodegradability.After 60 days of exposure to Penicillium sp.,foam containing both TEP and EG exhibited a mass loss of 9.39%,indicating that the incorporation of flame retardants did not negatively impact its biodegradability.展开更多
Propylene oxide(PO),with its reactive three-membered epoxide functional group,exhibits remarkable functional versatility and serves as a crucial bridge connecting the gaps between fossil energy utilization and chemica...Propylene oxide(PO),with its reactive three-membered epoxide functional group,exhibits remarkable functional versatility and serves as a crucial bridge connecting the gaps between fossil energy utilization and chemical intermediate generation for new material innovation [1].For instance,PO's downstream derivatives,such as polyether polyols,carbonic esters,and polyurethanes,are widely utilized in wind power generation,battery electrolytes,solar cells,and CO_(2)-based degradable polymers,contributing to sustainable decarbonization in industry [2].展开更多
A versatile heteropoly acid(H_(3)PMo_(12)O_(40))-catalyzed coupling of diarylmethanols with epoxides was established for the synthesis of polyaryl-substituted aldehydes.Furthermore,the catalytic system was also suitab...A versatile heteropoly acid(H_(3)PMo_(12)O_(40))-catalyzed coupling of diarylmethanols with epoxides was established for the synthesis of polyaryl-substituted aldehydes.Furthermore,the catalytic system was also suitable for the reaction of diarylmethanols and diols/aldehydes.The application of such an earthabundant,readily accessible,and nontoxic catalyst provides a green approach for the construction of polyaryl-substituted aldehydes.展开更多
Copolymerization is a commonly employed method for optimizing the properties of polymer materials.Incorporating ether segments into polyesters main chain to obtain polyether-polyester copolymers is an effective strate...Copolymerization is a commonly employed method for optimizing the properties of polymer materials.Incorporating ether segments into polyesters main chain to obtain polyether-polyester copolymers is an effective strategy to realize the integration of multiple properties of polyester and polyether,and to develop more high-performance,multi-purpose polymer materials.Herein,the synthesis of poly(ether-ester)s is accessible by employing the biphenyl-linked heterodinuclear salen Cr-AI complex in the presence of PPNCI for the copolymerization of epoxides and£-caprolactone(CL).Monitoring the copolymerization process reveals that catalyst 1 exhibited good performance for the copolymerization of epoxides and CL,affording copolymers with a gradient sequence structure.The dynamic thermomechanical analysis(DMA)study indicates the obtained poly(ether-ester)s possess enhanced flexibility compared with the block copolymers or blend of PPO and PCL homopolymers with the same ratio.This study provides a theoretical basis for the preparation of high-performance polymer materials.展开更多
Silk fabrics is finished with epoxide TDEA or TDEB. By the determination of washing fastness, DSC, IR spectrum and amino acid contents tests, TDEA or TDEB is confirmed to react with silk fibroin. By means of tests of ...Silk fabrics is finished with epoxide TDEA or TDEB. By the determination of washing fastness, DSC, IR spectrum and amino acid contents tests, TDEA or TDEB is confirmed to react with silk fibroin. By means of tests of silk fibroin swelling and solubility in some solvents, crosslinking reactions between TDEA or TDEB and silk fibroin arc further proved, which is obviously responsible to the increase of wet-crease recovery of silk fabrics finished with epoxide TDEA or TDEB.展开更多
A highly effective and mild protocol for ring opening of epoxides with NH4SCN in the presence of catalytic amount of a multi- site phase-transfer catalyst, α,α＇,α＂-N-hexakis（triethylammoniummethylene chloride）-...A highly effective and mild protocol for ring opening of epoxides with NH4SCN in the presence of catalytic amount of a multi- site phase-transfer catalyst, α,α＇,α＂-N-hexakis（triethylammoniummethylene chloride）-melamine, is developed. A variety of ^-hydroxy thiocyanates as important intermediates in agricultural and pharmaceutical chemistry were obtained in high yields with excellent regioselectivity and in short reaction times. 2009 Ali Reza Kiasat. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
Metal(Al,Ti,Zr)triflate grafted mesoporous SBA‐15(AlTf/S,TiTf/S,ZrTf/S)samples were synthesizedas inexpensive solid acid materials by a simple one‐pot‐two‐step synthesis methodology.These materials were characteri...Metal(Al,Ti,Zr)triflate grafted mesoporous SBA‐15(AlTf/S,TiTf/S,ZrTf/S)samples were synthesizedas inexpensive solid acid materials by a simple one‐pot‐two‐step synthesis methodology.These materials were characterized by X‐ray diffraction,N2‐sorption,thermogravimetric analysis,Fourier transform infrared spectroscopy(FT‐IR),in‐situ pyridine FT‐IR spectroscopy,and elementalanalysis.ZrTf/S was found to be a highly efficient and reusable solid acid catalyst for ring opening ofepoxides with amines and alcohols and producedβ‐amino alcohols andβ‐alkoxy alcohols respectivelyunder ambient reaction conditions.The ZrTf/S catalyst showed the highest activity,whichwas attributed to its high acidity compared with that of the Ti and Al containing samples.展开更多
Silica sulfuric acid was developed as a stable and efficient heterogeneous catalyst in organic synthesis. This solid acid catalyzed the regioselective ring opening of epoxides by thiocyanate anion to give thiocyanohyd...Silica sulfuric acid was developed as a stable and efficient heterogeneous catalyst in organic synthesis. This solid acid catalyzed the regioselective ring opening of epoxides by thiocyanate anion to give thiocyanohydrins as key intermediates in agricultural and pharmaceutical chemistry in high yields under solvent-free conditions.展开更多
基金financially supported by the National Natural Science Foundation of China(No.22161040)Natural Science Foundation of Gansu(No.24JRRA125)Science Research Project of Northwest Normal University(No.NWNU-LKZD2021-3)。
文摘The ring-opening alternating copolymerization(ROAC)of 3,4-dihydrocoumarin(DHC)/epoxides has been successfully developed using an imidazolium salt of 1-ethyl-3-methylimidazolium chloride(EMIMCl)as a catalyst.The resulting copolymer has a molecular weight of 13.7kg·mol^(-1),a narrow molecular weight distribution of 1.03 and a strictly alternating structure.The MALDI-TOF MS characterization and DFT calculations including electrostatic potential(ESP),hydrogen-atom abstraction(HAA),independent gradient model based on hirshfeld partition(IGMH)and atoms-in-molecules(AIM)analysis were used to investigate the metal-free catalytic process.The synergistic effect of anions and cations of EMIMCl for ROAC of DHC and epoxides was demonstrated.This study provides a metal-free catalytic system for the facile synthesis of alternating polyesters from DHC.
文摘Polyhydroxyalkanoate(PHA),a well-known biodegradable polymer,featuresβ-lactones as its monomers,which can be selectively synthesized through ring-expansion carbonylation of epoxides using well-defined[Lewis acid]^(+)[Co(CO)_(4)]^(-)catalysts.However,the decomposition of[Co(CO)_(4)]^(-)species at temperatures exceeding 80℃presents a hurdle for the development of commercially viable processes under high-temperature reaction conditions to reduce reaction time.Drawing insights from stable{(acyl)Co(CO)n}intermediates involved in historical HCo(CO)_(4)-catalyzed hydroformylation processes,we sought to the high-temperature catalytic activity of epoxide ring-expansion carbonylation.The developed catalyst system,[(acetyl)Co(CO)_(2)dppp]and[(TPP)CrCl],exhibited exceptional catalytic performance with an unprecedented initial turnover frequency of 4700 h^(-1)at 100℃and a turnover numbers of 93000.Notably,the catalyst displayed outstanding stability,operating at 80℃for 168 h while selectively generatingβ-lactones.
基金the National Natural Science Foundation of China (Nos. 22225106, 22301193)Fundamental Research Funds from Sichuan University (No. 2020SCUNL102)the Fundamental Research Funds for the Central Universities。
文摘Herein, we report the first visible-light photoredox-catalyzed carboxylation of aryl epoxides with CO_(2)to synthesize hydroxy acid derivatives. A variety of valuable β-, γ-, δ-, ε–hydroxy acid derivatives are obtained in moderate to high yields under mild conditions. This protocol shows noteworthy functionalgroup compatibility, high chemo-and regioselectivities under transition-metal-free conditions with an inexpensive organo-dye as photosensitizer. Mechanistic studies indicate that the benzylic carbanion is generated as an intermediate via the sequential single electron transfer(SSET) process.
基金supported by the National Science and Technology Support Project of China(2013BAC11B03)the National Natural Science Foundation of China(21401054,21476065,21273067)the Graduate Student Scientific Research Innovation Fund Project of Hunan Province(CX2015B082)~~
文摘The aim of ＂green chemistry＂ and ＂atom economy＂ is to utilize carbon dioxide and replace harmful reactants such as CO and phosgene for the production of cyclic carbonates. In this paper, metal-free catalysts including organic bases, ionic liquids, supported catalysts, organic copolymers and carbon materials for the synthesis of cyclic carbonates by the cycloaddition of carbon dioxide to epoxides are reviewed. Recent advances in the design of the catalysts and the understanding of the reaction mechanism are summarized and discussed. The synergistic effects of organic bases and hydrogen bond donors, organic bases and nucleophilic anions, hydrogen bond donors and nucleophilic anions and active components and supports are highlighted. The challenge is to develop metal-free catalysts suitable for carbon dioxide capture and fixation. The ultimate goal is to synthesize cyclic carbonates in a flow reactor directly using carbon dioxide from industrial flue gas at ambient temperature and atmospheric pressure. By using synergetic effects, a multi-functional approach can meet the design strategy of metal-free catalysts for carbon dioxide adsorption and activation as well as epoxide ring opening.
文摘Three new cyclohexene epoxides,polysyphoside A,B and C,along with a known compound crotepoxide(4),were isolated from Piper polysyphorum C.DC.Based on spectroscopic analysis,their structures were established as 1-benzoyloxymethylene-2-hydroxy-3-benzoyloxy-1,6- epoxycyclohex-4-ene(1),1-benzoyloxymethylene-2-hydroxy-5-benzoyloxy-1,6-epoxycyclohex-3-ene (2)and 2-hydroxy-3-benzoyloxymethylene-5-benzoyloxy-1,6-epoxycyclohex-3-ene(3),respectively.It was the first time that(1),(2)and(3)had been isolated from a natural source.
基金financially supported by the National Natural Science Foundation of China(Nos.21134002 and 21174023)Program for Changjiang Scholars and Innovative Research Teams in University(No.IRT13008)the Chang Jiang Scholars Program(No.T2011056)from the Ministry of Education of China
文摘This report presents a detailed density functional theory （DFT） study on the difference in regioselectivity for the copolymerization reactions of styrene oxide versus propylene oxide with CO2 utilizing binary （salen）cobalt（III） catalyst systems. This study focuses on the discrepancy of regioselective ring-opening of two terminal epoxides during the copolymerization with CO2. It was found that the nucleophilic ring-opening of styrene oxide occurred predominantly at the methine C a--O bond due to the election delocalization of phenyl group to stabilize the transition state for the methine C--O bond cleavage.
基金Funded by the National Natural Science Foundation of China(No.21865017)。
文摘[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane was synthesized,using tert-butyldimethylsilane(TBDMS)and 1,2-epoxy-4-vinylcyclohexane(EVC)as the main raw materials and tris(triphenylphosphine)chlororhodium(I)[RhCl(Ph3P)3]as the catalyst.[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane is a novel kind of silicon-containing epoxide.The factors affecting the reaction yield,such as catalyst use,reaction time and reaction temperature,were investigated,and the synthesized product was characterized and analyzed by FT-IR and 1H-NMR.A series of amine-curing resins were prepared with[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane,bisphenol A epoxy resin(E-51)and modified amine(593 amine).The mechanical properties of cured splines with the different proportions of amine-curing resins were tested.When the content of 593 amine was 20%,the content of E-51 was 75%and the amount of[2-(3,4-epoxy-cyclohexyl)ethyl]dimethyltert-butylsilane was 5%,the mechanical properties of the cured splines were the best with the tensile strength being 23.3 MPa,the elongation at break being 7.8%,and the Young's modulus being 421.3 MPa.
基金supported by the Applied Basic Research Foundation of Guangdong Province(No.2019A1515110551)the Science Foundation for Distinguished Scholars of Dongguan University of Technology(No.196100041051).
文摘In the context of peaking carbon dioxide emissions and carbon neutrality,development of feasible methods for converting CO_(2)into high value-added chemicals stands out as a hot subject.In this study,P[D+COO^(−)][Br^(−)][DBUH^(+)],a series of novel heterogeneous dual-ionic poly(ionic liquid)s(PILs)were synthesized readily from 2-(dimethylamino)ethyl methacrylate(DMAEMA),bromo-substituted aliphatic acids,organic bases and divinylbenzene(DVB).The structures,compositions and morphologies were characterized or determined by nuclear magnetic resonance(NMR),thermal gravimetric analysis(TGA),infrared spectroscopy(IR),scanning electron microscopes(SEM),and Brunauer-Emmett-Teller analysis(BET),etc.Application of the P[D+COO^(−)][Br^(−)][DBUH^(+)]series as catalysts in converting CO_(2)into cyclic carbonates showed that P[D+COO^(−)][Br^(−)][DBUH^(+)]-2/1/0.6was able to catalyze epiclorohydrin-CO_(2)cycloaddition the most efficiently.This afforded chloropropylene carbonate(CPC)in 98.4%yield with≥99%selectivity in 24 hr under solvent-and additive-free conditions at atmospheric pressure.Reusability experiments showed that recycling of the catalyst 6 times only resulted in a slight decline in the catalytic performance.In addition,it could be used for the synthesis of a variety of differently substituted cyclic carbonates in good to excellent yields.Finally,key catalytic active sites were probed,and a reasonable mechanism was proposed accordingly.In summary,this work poses an efficient strategy for heterogenization of dual-ionic PILs and provides amild and environmentally benign approach to the fixation and utilization of carbon dioxide.
基金financially supported by the National Natural Science Foundation of China(Nos.22271021,21971024,22201021)the Doctoral Scientific Research Foundation of Liaoning Province(No.2022-BS-302)。
文摘Selective oxidation of olefin to epoxides is an important reaction in industry,however,developing heterogeneous catalysts to achieve the effective catalysis for this reaction under O_(2)atmosphere at room temperature is challenging but highly desired.In this work,two novel 2D cobalt metal-organic complexes,namely[Co(L)(5-HIP)]·2H_(2)O(Co-MOC-1)and[Co(L)(BTEC)_(0.5)]·H_(2)O(Co-MOC-2)(L=(E)-4,4-(ethene-1,2-diyl))bis(N-(pyridin-3-yl)benzamide;5-H_(2)HIP=5-hydroxyisophthalic acid;H4BTEC=pyromellitic acid)were designed and synthesized through hydrothermal method,which exhibited different metal coordination modes(4-coordinate and 5-coordinate,respectively)and 2D layer structures directed by different carboxylates co-ligands.Two Co-MOCs can serve as heterogeneous catalysts for the selective oxidation of olefins to epoxides at room temperature using O_(2)as oxidant.Furthermore,a higher catalysis activity of Co-MOC-1 than Co-MOC-2(96.7%vs.90.2%yield of 1,2-epoxycyclooctane)was observed,which may be attributed to the coordination unsaturated Co centers,the less coordination number and larger interlayer spacing of Co-MOC-1.
基金supported by the National Natural Science Foundation of China(U23B20156,52174033).
文摘Resin plugging agents play a pivotal role in addressing casing damage in oil and gas fields.However,the widespread use of epoxy resin is constrained by its high cost and non-renewable origin,while plant-based resins often suffer from inadequate mechanical properties,which limit their effectiveness in such applications.This study introduces BEOPA,an innovative,renewable,high-strength resin plugging agent derived from epoxidized soybean oil(ESO)and enhanced with bisphenol A-type benzoxazine(BZ).In this study,the synthesis process,reactionmechanism,and application performance of this novelmaterial are systematically presented,explored and optimized.It is shown that the optimal formulation of BEOPA includes 41.4 wt%ESO,24.8 wt%BZ,24.8 wt%methylhexahydrophthalic anhydride(MHHPA),8.2 wt%styrene(ST),and 0.8 wt%N,N-dimethylbenzylamine(BDMA),yielding an impressive compressive strength of 93.7 MPa.The integration of ESO and BZ creates an intricate and robust double crosslinking network,significantly enhancing material strength and durability.BEOPA exhibits a tunable curing time,ranging from 0.5 to 15 h,with viscosities below 300 mPa⋅s at 25℃and 75mPa⋅s at 50℃.Furthermore,it demonstrates exceptional thermal stability within the 100℃-150℃range,even in environments with mineral salt concentrations as high as 43,330 mg/L.Remarkably,BEOPA achieves superior plugging performance,sustaining breakthrough pressures exceeding 29.7 MPa in 1 mm crack cores.
基金supported by the National Natural Science Foundation of China(82274069 and 82003580)Shenzhen science and technology research and development funds(JCYJ20190808171803553 and 2022071718149001)+4 种基金Young Scientific and Technological Talents(Level Two)in Tianjin(QN20230212)Tianjin Education Commission Research Program Project(2024KJ004)Young Elite Scientists Sponsorship Program by China Association of Chinese Medicine(2022-QNRC2-B09)“1+X”Research Project of the Second Hospital of Dalian Medical University(2024JJ11PT005)Eaglet Plan Project of Tianjin University of Traditional Chinese Medicine(XJS2024101)。
文摘Objective:Soluble epoxide hydrolase(sEH)emerges as a target of interest for inflammatory diseases.Piperine is a natural amide alkaloid from Piper nigrum and displays an inhibitory effect toward sEH,its chemical structural transformation was carried out in order to obtain a library of sEH inhibitors based on its skeleton.Methods:Structural transformation of piperine was carried out by chemical methods,and piperine derivatives were assayed for their sEH potentials.A mouse acute lung injury model was constructed by lipopolysaccharide(LPS).Hematoxylin and eosin(H&E)staining,immunofluorescence staining,Western Blot,and enzyme-linked immunosorbent assay were used for investigating the protective potential of sEH inhibitor 11h.Results:Piperine derivatives 11e,11h,11j,and 11o showed inhibitory potentials toward sEH with values of half maximal inhibitory concentration(IC50)from 20 to 70 nM.Compound 11h attenuated the pathological course of LPS-mediated acute lung injury(ALI)in vivo.Furthermore,levels of cytokines tumor necrosis factor alpha(TNF-α),interleukin 6(IL-6),myeloperoxidase(MPO),and lactate dehydrogenase(LDH)were decreased after administration of 11h.The LPS-mediated inflammation and redox unbalance,including expressions of cyclooxygenase-2(COX-2),heme oxygenase-1(HO-1),intercellular cell adhesion molecule-1(ICAM-1),vascular cell adhesion molecule-1(VCAM-1),p-p65/p65,glutamate-cysteine ligase modifier subunit(GCLM),and nuclear factor erythroid-2-related factor 2(Nrf2),were ameliorated through nuclear factor kappa B(NF-κB)and Nrf2 pathways via enhancing levels of epoxyeicosatrienoic acids(EETs)in LPS-exposed ALI mice after compound 11h treatment.Molecular docking demonstrated that the aromatic unsaturated group of 11h occupied a hydrophobic pocket and its urea group formed three hydrogen bonds with Asp333,Tyr381,and Tyr465,which stabilized the active conformation of the ligand.Conclusions:These findings demonstrated that compound 11h may serve as a lead compound for developing sEH inhibitors and treating inflammation related to diseases,such as ALI.
基金funded by the Latvian State Institute of Wood Chemistry Bioeconomic grant no.04-24“Development of Composites from Polymer Resin Synthesized from Tall Oil Fatty Acids and Reinforced with Various Fillers”(FiTeCo).
文摘Studies on the use of renewable materials for various applications,including polymers,have gained momentum due to global climate change and the push towards a circular economy.In this study,polymer resins were developed through Michael 1,4-addition.The precursors were synthesized from tall oil-based acetoacetates derived from epoxidized tall oil fatty acids or their methyl esters.Two different epoxidation methods were employed:enzymatic epoxidation of tall oil fatty acids and ion-exchange resin epoxidation of tall oil fatty acid methyl esters.Following oxirane opening and transesterification with trimethylolpropane,further esterification or transesterification was carried out to obtain the acetoacetates.These synthesized acetoacetates were then reacted with acrylates of various functionalities to obtain polymer resins with differing degrees of crosslinking.The developed polymer resins were characterized using differential scanning calorimetry,dynamic mechanical analysis,and thermogravimetric analysis.The results indicated that the glass transition temperature and storage modulus of the polymer resins were significantly influenced by both the functionality of the acrylates used and the epoxidation technique employed.Higher acrylate functionality resulted in increased stiffness,while enzymatic epoxidation enhanced the polymer’s mechanical properties,nearly doubling the storage modulus,achieving approximately 470 MPa,compared to the ion-exchange resin technique.Therefore,selecting the appropriate acrylate functionality and epoxidation method could tailor the mechanical properties of the polymer resins.
基金financially supported by the National Natural Science Foundation of China(No.32460363)Yunnan Province Agricultural Joint Key Foundation(No.202401BD070001-029)+3 种基金as well as the Yunnan Provincial Youth top talent project(No.YNWR-QNBJ-2020-166)Foreign Expert Workstation(No.202305 AF150006)111 project(No.D21027)Yunnan Province Natural Science Key Foundation(No.202301AS070043)。
文摘In this study,epoxidized soybean oil(ESO)and ricinoleic acid(RA)were used to synthesize polyol esters,designated ESO-RA(ER)resin.The esters were further crosslinked with 4,4-diphenylmethane diisocyanate(PMDI)to create a biodegradable flame-retardant thermoset foam,referred to as ESO-RA-PMDI(ERP)foam,using water as a foaming agent.Additionally,flame retardants such as triethyl phosphate(TEP)and expanded graphite(EG)have been combined for foam preparation without the need for catalysts or foaming agents.The study findings showed that the incorporation of TEP and EG diminished the pulverization ratio while augmenting the compressive strength and shore hardness.Furthermore,the ERP foam exhibited exceptional flame retardant characteristics,as evidenced by a reported limiting oxygen index(LOI)value of 30.6vol%.A peak heat release rate of 97.12 kW/m^(2)was reported during the fire test.Significantly,a low peak smoke production rate(pSPR)of 0.026m^(2)/s and a total smoke production(TSP)of 0.62 m^(2)were achieved.In addition,ERP foam exhibited exceptional ultraviolet(UV)resistance,thermal insulation,and biodegradability.After 60 days of exposure to Penicillium sp.,foam containing both TEP and EG exhibited a mass loss of 9.39%,indicating that the incorporation of flame retardants did not negatively impact its biodegradability.
基金supported by the National Natural Science Foundation of China (29792072, 22278441, 22478452)National Key Research and Development Program of China (937) (2006CB202508)the SINOPEC Project (419019-2, 413108)。
文摘Propylene oxide(PO),with its reactive three-membered epoxide functional group,exhibits remarkable functional versatility and serves as a crucial bridge connecting the gaps between fossil energy utilization and chemical intermediate generation for new material innovation [1].For instance,PO's downstream derivatives,such as polyether polyols,carbonic esters,and polyurethanes,are widely utilized in wind power generation,battery electrolytes,solar cells,and CO_(2)-based degradable polymers,contributing to sustainable decarbonization in industry [2].
基金the financial support from the National Natural Science Foundation of China(Nos.21871026,21971224)Research Found of East China University of Technology(Nos.DHBK2019265,DHBK2019267,DHBK2019264)。
文摘A versatile heteropoly acid(H_(3)PMo_(12)O_(40))-catalyzed coupling of diarylmethanols with epoxides was established for the synthesis of polyaryl-substituted aldehydes.Furthermore,the catalytic system was also suitable for the reaction of diarylmethanols and diols/aldehydes.The application of such an earthabundant,readily accessible,and nontoxic catalyst provides a green approach for the construction of polyaryl-substituted aldehydes.
基金the National Natural Science Foundation of China(Nos.21722402 and 21674015).
文摘Copolymerization is a commonly employed method for optimizing the properties of polymer materials.Incorporating ether segments into polyesters main chain to obtain polyether-polyester copolymers is an effective strategy to realize the integration of multiple properties of polyester and polyether,and to develop more high-performance,multi-purpose polymer materials.Herein,the synthesis of poly(ether-ester)s is accessible by employing the biphenyl-linked heterodinuclear salen Cr-AI complex in the presence of PPNCI for the copolymerization of epoxides and£-caprolactone(CL).Monitoring the copolymerization process reveals that catalyst 1 exhibited good performance for the copolymerization of epoxides and CL,affording copolymers with a gradient sequence structure.The dynamic thermomechanical analysis(DMA)study indicates the obtained poly(ether-ester)s possess enhanced flexibility compared with the block copolymers or blend of PPO and PCL homopolymers with the same ratio.This study provides a theoretical basis for the preparation of high-performance polymer materials.
文摘Silk fabrics is finished with epoxide TDEA or TDEB. By the determination of washing fastness, DSC, IR spectrum and amino acid contents tests, TDEA or TDEB is confirmed to react with silk fibroin. By means of tests of silk fibroin swelling and solubility in some solvents, crosslinking reactions between TDEA or TDEB and silk fibroin arc further proved, which is obviously responsible to the increase of wet-crease recovery of silk fabrics finished with epoxide TDEA or TDEB.
基金the partial support of this work by Shahid Chamran Research Council
文摘A highly effective and mild protocol for ring opening of epoxides with NH4SCN in the presence of catalytic amount of a multi- site phase-transfer catalyst, α,α＇,α＂-N-hexakis（triethylammoniummethylene chloride）-melamine, is developed. A variety of ^-hydroxy thiocyanates as important intermediates in agricultural and pharmaceutical chemistry were obtained in high yields with excellent regioselectivity and in short reaction times. 2009 Ali Reza Kiasat. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
基金supported by the CAS President’s International Fellowship Initiative (2016PT028)the National Natural Science Foundation of China (21273225 and 21403219)~~
文摘Metal(Al,Ti,Zr)triflate grafted mesoporous SBA‐15(AlTf/S,TiTf/S,ZrTf/S)samples were synthesizedas inexpensive solid acid materials by a simple one‐pot‐two‐step synthesis methodology.These materials were characterized by X‐ray diffraction,N2‐sorption,thermogravimetric analysis,Fourier transform infrared spectroscopy(FT‐IR),in‐situ pyridine FT‐IR spectroscopy,and elementalanalysis.ZrTf/S was found to be a highly efficient and reusable solid acid catalyst for ring opening ofepoxides with amines and alcohols and producedβ‐amino alcohols andβ‐alkoxy alcohols respectivelyunder ambient reaction conditions.The ZrTf/S catalyst showed the highest activity,whichwas attributed to its high acidity compared with that of the Ti and Al containing samples.
文摘Silica sulfuric acid was developed as a stable and efficient heterogeneous catalyst in organic synthesis. This solid acid catalyzed the regioselective ring opening of epoxides by thiocyanate anion to give thiocyanohydrins as key intermediates in agricultural and pharmaceutical chemistry in high yields under solvent-free conditions.
