The title compounds 3 and 4 condensed with aromatic aldehydes to give a--aroylsicinnamoyl ketene cyclic dithioacetals 5 and 6 with sodium ethoxide as the base. The stereochemistryofs and 6 was assigned as E-configurat...The title compounds 3 and 4 condensed with aromatic aldehydes to give a--aroylsicinnamoyl ketene cyclic dithioacetals 5 and 6 with sodium ethoxide as the base. The stereochemistryofs and 6 was assigned as E-configuration by 1H NMR.展开更多
The reactions of α-(alkoxysilyl)allyl anions 4 with electrophiles were studied. α-Alkylation with alkyl halides was favoured, whereas γ-selection was achieved in the reaction with aldehydes.
The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy i...The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy is dependent on using a platinumdivinyltetramethyldisiloxane complex(Pt^(0)-DVTMS)as the precursor,which we demonstrate can be removed through a H_(2)-treatment under mild conditions.This,in turn,allowed for the synthesis of catalysts with well dispersed Pt particles.The presence of FeO_(x) species also aided Pt dispersion;when coated onto SBA-15,FeO_(x) strongly interacted with dissociated Pt species,inhibiting both Pt aggregation and metal leaching.Using cinnamaldehyde as a modelα,β-unsaturated aldehyde,it was demonstrated that this catalyst was highly selective towards the unsaturated alcohol and no obvious loss in activity was observed over five recycles.This catalyst was determined to be significantly more effective than an analogous catalyst prepared using chloroplatinic acid as a precursor,evidencing the importance of using the Pt0-DVTMS precursor.We corroborate the excellent catalytic performance to highly dispersed Pt-species,whereby Pt0 and Pt^(2+) play a critical role in activating H_(2) and the C=O bond.This research demonstrates that the Pt precursor can have a significant impact on the physicochemical properties and thus,the performance of the final catalyst.It also evidences how metal support interactions can dramatically influence selectivity in such hydrogenation reactions.This novel catalyst preparation protocol,using a DVTMS ligand for Pt impregnation,offers a facile approach to the design of multi-component heterogeneous catalysts.展开更多
As an important technology in fine chemical production,the selective hydrogenation ofα,β-unsaturated aldehydes has attracted much attention in recent years.In the process ofα,β-unsaturated aldehyde hydrogenation,a...As an important technology in fine chemical production,the selective hydrogenation ofα,β-unsaturated aldehydes has attracted much attention in recent years.In the process ofα,β-unsaturated aldehyde hydrogenation,a conjugated system is formed between>C=C<and>C=O,leading to hydrogenation at both ends of the conjugated system,which competes with each other and results in more complex products.Therefore,improving the reaction selectivity is also difficult in industrial fields.Recently,many researchers have reported that surface-active sites on catalysts play a crucial role inα,β-unsaturated aldehyde hydrogenation.This review attempts to summarize recent advances in understanding the effects of surface-active sites(SASs)over metal catalysts for enhancing the process of hydrogenation.The construction strategies and roles of SASs for hydrogenation catalysts are summarized.Particular attention has been given to the adsorption configuration and transformation mechanism ofα,β-unsaturated aldehydes on catalysts,which contributes to understanding the relationship between SASs and hydrogenation activity.In addition,recent advances in metal-supported catalysts for the selective hydrogenation ofα,β-unsaturated aldehydes to understand the role of SASs in hydrogenation are briefly reviewed.Finally,the opportunities and challenges will be highlighted for the future development of the precise construction of SASs.展开更多
Selective upgrading of C=O bonds to afford carboxylic acid is significant for the petrochemical industry and biomass utilization.Here we declared the efficient electrooxidation of biomass-derived aldehydes family over...Selective upgrading of C=O bonds to afford carboxylic acid is significant for the petrochemical industry and biomass utilization.Here we declared the efficient electrooxidation of biomass-derived aldehydes family over NiV-layered double hydroxides(LDHs) thin films.Mechanistic studies confirmed the hydroxyl active intermediate(-OH*) generated on the surface of NiV-LDHs films by employing electrochemical impedance spectroscopy and the electron paramagnetic resonance spectroscopy.By using advanced techniques,e.g.,extended X-ray absorption fine structure and high-angle annular dark-field scanning transmission electron microscopy,NiV-LDHs films with 2.6 nm could expose larger specific surface area.Taking benzaldehyde as a model,high current density of 200 mA cm^(-2)at 1.8 V vs.RHE,81.1% conversion,77.6% yield of benzoic acid and 90.8% Faradaic efficiency were reached,which was superior to most of previous studies.Theoretical DFT analysis was well matched with experimental findings and documented that NiV-LDHs had high adsorption capacity for the aldehydes to suppress the side reaction,and the aldehydes were oxidized by the electrophilic hydroxyl radicals formed on NiV-LDHs.Our findings offer a universal strategy for the robust upgrading of diverse biomass-derived platform chemicals.展开更多
As one of the few renewable aromatic resources,the research of depolymerization of lignin into highvalue chemicals has attracted extensive attention in recent years.Catalytic wet aerobic oxidation(CWAO)is an effective...As one of the few renewable aromatic resources,the research of depolymerization of lignin into highvalue chemicals has attracted extensive attention in recent years.Catalytic wet aerobic oxidation(CWAO)is an effective technology to convert lignin like sodium lignosulfonate(SL),a lignin derivative,into aromatic aldehydes such as vanillin and syringaldehyde.However,how to improve the yield of aromatic aldehyde and conversion efficiency is still a challenge,and many operating conditions that significantly affect the yield of these aromatic compounds have rarely been investigated systematically.In this work,we adopted the stirred tank reactor(STR)for the CWAO process with nano-CuO as catalyst to achieve the conversion of SL into vanillin and syringaldehyde.The effect of operating conditions including reaction time,oxygen partial pressure,reaction temperature,SL concentration,rotational speed,catalyst amount,and NaOH concentration on the yield of single phenolic compound was systematically investigated.The results revealed that all these operating conditions exhibit a significant effect on the aromatic aldehyde yield.Therefore,they should be regulated in an optimal value to obtain high yield of these aldehydes.More importantly,the reaction kinetics of the lignin oxidation was explored.This work could provide basic data for the optimization and design of industrial operation of lignin oxidation.展开更多
Selective hydrogenation of α, β-unsaturated aldehydes with modified Pd/C catalyst was developed.The reduction of C=O bond could be efficiently inhibited by the addition of carbonates,and high selectivity to the corr...Selective hydrogenation of α, β-unsaturated aldehydes with modified Pd/C catalyst was developed.The reduction of C=O bond could be efficiently inhibited by the addition of carbonates,and high selectivity to the corresponding saturated aldehydes was achieved under mild conditions.This protocol provides an alternative for efficient preparation of saturated aldehydes.展开更多
文摘The title compounds 3 and 4 condensed with aromatic aldehydes to give a--aroylsicinnamoyl ketene cyclic dithioacetals 5 and 6 with sodium ethoxide as the base. The stereochemistryofs and 6 was assigned as E-configuration by 1H NMR.
文摘The reactions of α-(alkoxysilyl)allyl anions 4 with electrophiles were studied. α-Alkylation with alkyl halides was favoured, whereas γ-selection was achieved in the reaction with aldehydes.
基金the National Natural Science Foundation(Nos.U1910202 and 21978194)the Key Research and Development Program of Shanxi Province(No.202102090301005)the Fund for Shanxi“1331 Project”.
文摘The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy is dependent on using a platinumdivinyltetramethyldisiloxane complex(Pt^(0)-DVTMS)as the precursor,which we demonstrate can be removed through a H_(2)-treatment under mild conditions.This,in turn,allowed for the synthesis of catalysts with well dispersed Pt particles.The presence of FeO_(x) species also aided Pt dispersion;when coated onto SBA-15,FeO_(x) strongly interacted with dissociated Pt species,inhibiting both Pt aggregation and metal leaching.Using cinnamaldehyde as a modelα,β-unsaturated aldehyde,it was demonstrated that this catalyst was highly selective towards the unsaturated alcohol and no obvious loss in activity was observed over five recycles.This catalyst was determined to be significantly more effective than an analogous catalyst prepared using chloroplatinic acid as a precursor,evidencing the importance of using the Pt0-DVTMS precursor.We corroborate the excellent catalytic performance to highly dispersed Pt-species,whereby Pt0 and Pt^(2+) play a critical role in activating H_(2) and the C=O bond.This research demonstrates that the Pt precursor can have a significant impact on the physicochemical properties and thus,the performance of the final catalyst.It also evidences how metal support interactions can dramatically influence selectivity in such hydrogenation reactions.This novel catalyst preparation protocol,using a DVTMS ligand for Pt impregnation,offers a facile approach to the design of multi-component heterogeneous catalysts.
基金supported by the National Natural Science Foundation of China (Grant No.21968007)the Guangxi Natural Science Foundation (Grant No.2020GXNSFDA297007)+1 种基金the Opening Project of Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology (Grant No.2023K002)Special funding for‘Guangxi Bagui Scholars’.
文摘As an important technology in fine chemical production,the selective hydrogenation ofα,β-unsaturated aldehydes has attracted much attention in recent years.In the process ofα,β-unsaturated aldehyde hydrogenation,a conjugated system is formed between>C=C<and>C=O,leading to hydrogenation at both ends of the conjugated system,which competes with each other and results in more complex products.Therefore,improving the reaction selectivity is also difficult in industrial fields.Recently,many researchers have reported that surface-active sites on catalysts play a crucial role inα,β-unsaturated aldehyde hydrogenation.This review attempts to summarize recent advances in understanding the effects of surface-active sites(SASs)over metal catalysts for enhancing the process of hydrogenation.The construction strategies and roles of SASs for hydrogenation catalysts are summarized.Particular attention has been given to the adsorption configuration and transformation mechanism ofα,β-unsaturated aldehydes on catalysts,which contributes to understanding the relationship between SASs and hydrogenation activity.In addition,recent advances in metal-supported catalysts for the selective hydrogenation ofα,β-unsaturated aldehydes to understand the role of SASs in hydrogenation are briefly reviewed.Finally,the opportunities and challenges will be highlighted for the future development of the precise construction of SASs.
基金supported by the National Natural Science Foundation of China(22078374,21776324)the Scientific and Technological Planning Project of Guangzhou(202206010145)+2 种基金the National Ten Thousand Talent Plan,Key-Area Research and Development Program of Guangdong Province(2019B110209003)the Guangdong Basic and Applied Basic Research Foundation(2019B1515120058,2020A1515011149)the Start-up Fund for Senior Talents in Jiangsu University(21JDG060)。
文摘Selective upgrading of C=O bonds to afford carboxylic acid is significant for the petrochemical industry and biomass utilization.Here we declared the efficient electrooxidation of biomass-derived aldehydes family over NiV-layered double hydroxides(LDHs) thin films.Mechanistic studies confirmed the hydroxyl active intermediate(-OH*) generated on the surface of NiV-LDHs films by employing electrochemical impedance spectroscopy and the electron paramagnetic resonance spectroscopy.By using advanced techniques,e.g.,extended X-ray absorption fine structure and high-angle annular dark-field scanning transmission electron microscopy,NiV-LDHs films with 2.6 nm could expose larger specific surface area.Taking benzaldehyde as a model,high current density of 200 mA cm^(-2)at 1.8 V vs.RHE,81.1% conversion,77.6% yield of benzoic acid and 90.8% Faradaic efficiency were reached,which was superior to most of previous studies.Theoretical DFT analysis was well matched with experimental findings and documented that NiV-LDHs had high adsorption capacity for the aldehydes to suppress the side reaction,and the aldehydes were oxidized by the electrophilic hydroxyl radicals formed on NiV-LDHs.Our findings offer a universal strategy for the robust upgrading of diverse biomass-derived platform chemicals.
基金supported by the National Key Research and Development Program of China(2019YFA0210302)the National Natural Science Foundation of China(21878009).
文摘As one of the few renewable aromatic resources,the research of depolymerization of lignin into highvalue chemicals has attracted extensive attention in recent years.Catalytic wet aerobic oxidation(CWAO)is an effective technology to convert lignin like sodium lignosulfonate(SL),a lignin derivative,into aromatic aldehydes such as vanillin and syringaldehyde.However,how to improve the yield of aromatic aldehyde and conversion efficiency is still a challenge,and many operating conditions that significantly affect the yield of these aromatic compounds have rarely been investigated systematically.In this work,we adopted the stirred tank reactor(STR)for the CWAO process with nano-CuO as catalyst to achieve the conversion of SL into vanillin and syringaldehyde.The effect of operating conditions including reaction time,oxygen partial pressure,reaction temperature,SL concentration,rotational speed,catalyst amount,and NaOH concentration on the yield of single phenolic compound was systematically investigated.The results revealed that all these operating conditions exhibit a significant effect on the aromatic aldehyde yield.Therefore,they should be regulated in an optimal value to obtain high yield of these aldehydes.More importantly,the reaction kinetics of the lignin oxidation was explored.This work could provide basic data for the optimization and design of industrial operation of lignin oxidation.
基金supported by the National High Technology Research and Development Program of China(863 Project)(No.2007AA03Z345)the Scientific Research Project for Institute of Higher Education of Education Bureau,Liaoning(No.LT2010021)the Fundamental Research Funds for Dalian University of Technology(No.DUT10RC(3)107)
文摘Selective hydrogenation of α, β-unsaturated aldehydes with modified Pd/C catalyst was developed.The reduction of C=O bond could be efficiently inhibited by the addition of carbonates,and high selectivity to the corresponding saturated aldehydes was achieved under mild conditions.This protocol provides an alternative for efficient preparation of saturated aldehydes.