The work is dedicated to develop a one-step eco-friendly method to prepare antibacterial polyethylene terephthalate(PET).We report a one-step eco-friendly method to manufacture antibacterial PET via on-line amination ...The work is dedicated to develop a one-step eco-friendly method to prepare antibacterial polyethylene terephthalate(PET).We report a one-step eco-friendly method to manufacture antibacterial PET via on-line amination reaction by melt coextrusion.Beside evenly mixing of poly(hexamethylene guanidine)(PHMG)and PET in the melt coextrusion procedure,the amination reaction also occurred between PHMG and PET under high temperature(230-270℃).The antibacterial ability of composite PET showed obvious PHMG concentration dependence,and antibacterial activity reached more than 99%when PHMG content was 2.5 wt%.Moreover,LIVE/DEAD fluorescence test further confirmed that the composite PET could kill bacteria quickly and efiectively(within 30 min);while negligible cytotoxicity was observed to HSF and HUVEC cells.Onestep eco-friendly fabrication of composite antibacterial PET was accomplished by on-line melt coextrusion.The composite antibacterial PET has potential use in multiple fields to combat with pathogenic including textiles,packaging materials,decoration materials and biomedical devices,etc.展开更多
The effects of RE modified mordenite catalysts on the activity and selectivity of amination reaction at atmospheric pressure in a fixed bed reactor were studied. The experimental result shows that the Y modified mor...The effects of RE modified mordenite catalysts on the activity and selectivity of amination reaction at atmospheric pressure in a fixed bed reactor were studied. The experimental result shows that the Y modified mordenite catalyst exhibits very good activity and selectivity to dimethylamine(DMA). The results of the catalyst characterization demonstrate that the rare earth modification of mordenite mainly causes the changes of B acidic sites in mordenite. The crystal structure and the Si/Al ratio on the surface of mordenite basically remain unchanged after mordenite is modified by rare earth elements. Rare earth modification improves the thermal stability and prolongs the life of the catalyst.展开更多
An optimization study on the amination reaction of epoxy polyisobutylene for synthesis of polyisobutylene amine is presented. The experimental results indicate that n-butanol and ethylenediamine are the suitable solve...An optimization study on the amination reaction of epoxy polyisobutylene for synthesis of polyisobutylene amine is presented. The experimental results indicate that n-butanol and ethylenediamine are the suitable solvent and amination agents for the reaction, respectively. The reaction yield of the amination reaction is notably increased with the enhanced molar ratio of either n-butanol against epoxy polyisobutylene or ethylenediamine against epoxy polyisobutylene. Also, the yield is enhanced with increasing temperature and time during the experimental range. Strikingly, the yield reaches as high as 91. 30% under optimal conditions; with the molar ratio of ethylenediamine, n-butanol and PIBO of 10∶ 6∶ 1, the reaction temperature of 150 ℃ and the reaction time of 6 h. In addition, the yield of the reaction is slightly decreased with the enhanced water content of the system. Accordingly, the mass concentration of water should be controlled within 1. 7% during the reaction.展开更多
Ni-Re/SiO2 catalysts with controllable Ni particle sizes(4.5–18.0 nm)were synthesized to investigate the effects of the particle size on the amination of monoethanolamine(MEA).The catalysts were characterized by vari...Ni-Re/SiO2 catalysts with controllable Ni particle sizes(4.5–18.0 nm)were synthesized to investigate the effects of the particle size on the amination of monoethanolamine(MEA).The catalysts were characterized by various techniques and evaluated for the amination reaction in a trickle bed reactor at 170℃,8.0 MPa,and 0.5 h^-1 liquid hourly space velocity of MEA(LHSVMEA)in NH3/H2 atmosphere.The Ni-Re/SiO2 catalyst with the lowest Ni particle size(4.5 nm)exhibited the highest yield(66.4%)of the desired amines(ethylenediamine(EDA)and piperazine(PIP)).The results of the analysis show that the turnover frequency of MEA increased slightly(from 193 to 253 h^-1)as the Ni particle sizes of the Ni-Re/SiO2 catalysts increased from 4.5 to 18.0 nm.Moreover,the product distribution could be adjusted by varying the Ni particle size.The ratio of primary to secondary amines increased from 1.0 to 2.0 upon increasing the Ni particle size from 4.5 to 18.0 nm.Further analyses reveal that the Ni particle size influenced the electronic properties of surface Ni,which in turn affected the adsorption of MEA and the reaction pathway of MEA amination.Compared to those of small Ni particles,large particles possessed a higher proportion of high-coordinated terrace Ni sites and a higher surface electron density,which favored the amination of MEA and NH3 to form EDA.展开更多
Heterocyclic ketene aminals 1 react with aryl azides 2 to give the titled compounds 3,and in some cases also with the formation of fused heterocycles 4.
The anion of heterocyclic ketene aminals reacted with 2,4-dini- tro-halobenzenes to give an arylated product through the radical nucleo- philic substitution confirmed by ESR spectroscopy,ESR-spin trapping techni- que,...The anion of heterocyclic ketene aminals reacted with 2,4-dini- tro-halobenzenes to give an arylated product through the radical nucleo- philic substitution confirmed by ESR spectroscopy,ESR-spin trapping techni- que,and depression of the reaction rate by the addition of inhibitor.展开更多
Photoinduced charge transfer reaction of benzophenone(BP) with, mine was carried out in the vesicles of dicetyldimethylammonium bromide (DCDAB) over wide ranges of amine concentration (0. 01～4. 0M). Linear plots of ...Photoinduced charge transfer reaction of benzophenone(BP) with, mine was carried out in the vesicles of dicetyldimethylammonium bromide (DCDAB) over wide ranges of amine concentration (0. 01～4. 0M). Linear plots of φ^(-1) vs. [TEA]^(-1) at low concentration of amine (<0.02M) and Φ^(-1) vs. [TEA]^(-2) at high concentration were obtained. Kinetic data demonstrate that the electron transfer is promoted significantly by DCDAB vesicles and proton transfer becomes more efficient at high Rmlne concentrations, leading to a decrease of Kd/Kr and increase of Kh/Ke. The kinetic expressions of photoreaction of BP bound to DCDAB bilayer are developed.展开更多
A series of 2 (E) (4 hydroxy 3 methoxybenzylidene) 5 (N substituted ami nomethyl) cyclopentanones was synthesized and evaluated for the anti inflammatory activity. All of the target compounds were confirmed ...A series of 2 (E) (4 hydroxy 3 methoxybenzylidene) 5 (N substituted ami nomethyl) cyclopentanones was synthesized and evaluated for the anti inflammatory activity. All of the target compounds were confirmed by spectral analysis and elemental analysis. Preliminary pharmacological tests showed that several compounds exerted appreciable inhibitory effect on xylene induced ear edema in mice and that alteration of the substituents of anilines had significant influence in anti inflammatory potency.展开更多
The performance applications(e.g.,photocatalysis)of zirconium(Zr)and hafnium(Hf)based complexes are greatly hindered by the limited development of their structures and the relatively inert metal reactivity.In this wor...The performance applications(e.g.,photocatalysis)of zirconium(Zr)and hafnium(Hf)based complexes are greatly hindered by the limited development of their structures and the relatively inert metal reactivity.In this work,we constructed two ultrastable Zr/Hf-based clusters(Zr_(9)-TC4A and Hf_(9)-TC4A)using hydrophobic 4-tert-butylthiacalix[4]arene(H4TC4A)ligands,in which unsaturated coordinated sulfur(S)atoms on the TC4A^(4-)ligand can generate strong metal–ligand synergy with nearby active metal Zr/Hf sites.As a result,these two functionalized H4TC4A ligands modified Zr/Hf-oxo clusters,as catalysts for the amine oxidation reaction,exhibited excellent catalytic activity,achieving very high substrate conversion(>99%)and product selectivity(>90%).Combining comparative experiments and theoretical calculations,we found that these Zr/Hf-based cluster catalysts accomplish efficient amine oxidation reactions through synergistic effect between metals and ligands:(i)The photocatalytic benzylamine(BA)oxidation reaction was achieved by the synergistic effect of the dual active sites,in which,the naked S sites on the TC4A^(4-)ligand oxidize the BA by photogenerated hole and oxygen molecules are reduced by photogenerated electrons on the metal active sites;(ii)in the aniline oxidation reaction,aniline was adsorbed by the bare S sites on ligands to be closer to metal active sites and then oxidized by the oxygen-containing radicals activated by the metal sites,thus completing the catalytic reaction under the synergistic catalytic effect of the proximity metal–ligand.In this work,the Zr/Hf-based complexes applied in the oxidation of organic amines have been realized using active S atom-directed metal–ligand synergistic catalysis and have demonstrated very high reactivity.展开更多
Under the guidance of the finding that the tyrosine residues in proteins could undergo three-component Mannich-type reactions with formaldehyde and electron-rich aniline-containing compounds,which forms covalent bondi...Under the guidance of the finding that the tyrosine residues in proteins could undergo three-component Mannich-type reactions with formaldehyde and electron-rich aniline-containing compounds,which forms covalent bonding connections between the protein of interest and the aniline with high levels of selectivity under relatively mild conditions,an orange aromatic primary amine-containing acid dye AMODB was designed and readily synthesized.The molecular structure was characterized by FTIR,^1H NMR,mass spectrometry and elemental analysis.The synthesized dye and a similar control dye（C.I.Acid Yellow 11） without primary amine groups were applied to dye silk fabric by three dyeing processes：Mannich-type dyeing（with and without the addition of formaldehyde） and acidic dyeing.Their washing and rubbing fastness properties with different dyeing methods were examined and compared.It was found that the dyed silk fabric with AMODB by the Mannich-type dyeing showed higher color depth,better anti-stripping ability to DMF and better washing fastness than those of the dyed silk fabric with C.I.Acid Yellow 11 by acidic dyeing due to the covalent bond formation between the dye chromophore of AMODB and silk fiber.In addition,mild Mannich dyeing conditions suitable for silk（AMODB at 3%owf,75：1 liquor-to-goods ratio,dyebath pH 5.5,30℃,10 h） were provided.展开更多
A concise and efficient approach was developed for the synthesis of mono-substituted and di-substituted pyrimidines products via palladium-catalyzed amination of chloro-substituted 5-nitropyrimidines and amines. This ...A concise and efficient approach was developed for the synthesis of mono-substituted and di-substituted pyrimidines products via palladium-catalyzed amination of chloro-substituted 5-nitropyrimidines and amines. This synthetic methodology can produce various di-substituted pyrimidines in high yields with good functional group tolerance, and provide a complementary tool for the syntheses of important intermediates of nucleosides and purines with bioactivities.展开更多
An intramolecular organocatalytic enantioselective aza-Michael reaction of carbamates, sulfonamides and acetamides to a,b-unsaturated ketones was developed. This process is promoted by 9-amino-9-deoxy-epi-quinine and ...An intramolecular organocatalytic enantioselective aza-Michael reaction of carbamates, sulfonamides and acetamides to a,b-unsaturated ketones was developed. This process is promoted by 9-amino-9-deoxy-epi-quinine and diphenyl hydrogen phosphate to afford a straightforward and expeditious synthesis of several synthetically useful five-and six-membered heterocycles with excellent enantioselectivity（92%–97.5% ee） and very good yields（up to 99%）.展开更多
基金Funded by the National Natural Science Foundation of China(No.51703169)Key Program of Science and Technology of Jieyang City(No.2019016)Key Research and Development Program of Shandong Province of China(No.2019JZZY010338)。
文摘The work is dedicated to develop a one-step eco-friendly method to prepare antibacterial polyethylene terephthalate(PET).We report a one-step eco-friendly method to manufacture antibacterial PET via on-line amination reaction by melt coextrusion.Beside evenly mixing of poly(hexamethylene guanidine)(PHMG)and PET in the melt coextrusion procedure,the amination reaction also occurred between PHMG and PET under high temperature(230-270℃).The antibacterial ability of composite PET showed obvious PHMG concentration dependence,and antibacterial activity reached more than 99%when PHMG content was 2.5 wt%.Moreover,LIVE/DEAD fluorescence test further confirmed that the composite PET could kill bacteria quickly and efiectively(within 30 min);while negligible cytotoxicity was observed to HSF and HUVEC cells.Onestep eco-friendly fabrication of composite antibacterial PET was accomplished by on-line melt coextrusion.The composite antibacterial PET has potential use in multiple fields to combat with pathogenic including textiles,packaging materials,decoration materials and biomedical devices,etc.
文摘The effects of RE modified mordenite catalysts on the activity and selectivity of amination reaction at atmospheric pressure in a fixed bed reactor were studied. The experimental result shows that the Y modified mordenite catalyst exhibits very good activity and selectivity to dimethylamine(DMA). The results of the catalyst characterization demonstrate that the rare earth modification of mordenite mainly causes the changes of B acidic sites in mordenite. The crystal structure and the Si/Al ratio on the surface of mordenite basically remain unchanged after mordenite is modified by rare earth elements. Rare earth modification improves the thermal stability and prolongs the life of the catalyst.
基金The Natural Science Foundation of Jiangsu Province(No.BK20130602)the Project of the Collaborative Innovation Center of Suzhou Nano Science and Technology
文摘An optimization study on the amination reaction of epoxy polyisobutylene for synthesis of polyisobutylene amine is presented. The experimental results indicate that n-butanol and ethylenediamine are the suitable solvent and amination agents for the reaction, respectively. The reaction yield of the amination reaction is notably increased with the enhanced molar ratio of either n-butanol against epoxy polyisobutylene or ethylenediamine against epoxy polyisobutylene. Also, the yield is enhanced with increasing temperature and time during the experimental range. Strikingly, the yield reaches as high as 91. 30% under optimal conditions; with the molar ratio of ethylenediamine, n-butanol and PIBO of 10∶ 6∶ 1, the reaction temperature of 150 ℃ and the reaction time of 6 h. In addition, the yield of the reaction is slightly decreased with the enhanced water content of the system. Accordingly, the mass concentration of water should be controlled within 1. 7% during the reaction.
基金supported by the National Natural Science Foundation of China(21273227)Strategic Priority Research Program of Chinese Academy of Sciences(XDB17000000)~~
文摘Ni-Re/SiO2 catalysts with controllable Ni particle sizes(4.5–18.0 nm)were synthesized to investigate the effects of the particle size on the amination of monoethanolamine(MEA).The catalysts were characterized by various techniques and evaluated for the amination reaction in a trickle bed reactor at 170℃,8.0 MPa,and 0.5 h^-1 liquid hourly space velocity of MEA(LHSVMEA)in NH3/H2 atmosphere.The Ni-Re/SiO2 catalyst with the lowest Ni particle size(4.5 nm)exhibited the highest yield(66.4%)of the desired amines(ethylenediamine(EDA)and piperazine(PIP)).The results of the analysis show that the turnover frequency of MEA increased slightly(from 193 to 253 h^-1)as the Ni particle sizes of the Ni-Re/SiO2 catalysts increased from 4.5 to 18.0 nm.Moreover,the product distribution could be adjusted by varying the Ni particle size.The ratio of primary to secondary amines increased from 1.0 to 2.0 upon increasing the Ni particle size from 4.5 to 18.0 nm.Further analyses reveal that the Ni particle size influenced the electronic properties of surface Ni,which in turn affected the adsorption of MEA and the reaction pathway of MEA amination.Compared to those of small Ni particles,large particles possessed a higher proportion of high-coordinated terrace Ni sites and a higher surface electron density,which favored the amination of MEA and NH3 to form EDA.
文摘Heterocyclic ketene aminals 1 react with aryl azides 2 to give the titled compounds 3,and in some cases also with the formation of fused heterocycles 4.
文摘The anion of heterocyclic ketene aminals reacted with 2,4-dini- tro-halobenzenes to give an arylated product through the radical nucleo- philic substitution confirmed by ESR spectroscopy,ESR-spin trapping techni- que,and depression of the reaction rate by the addition of inhibitor.
文摘Photoinduced charge transfer reaction of benzophenone(BP) with, mine was carried out in the vesicles of dicetyldimethylammonium bromide (DCDAB) over wide ranges of amine concentration (0. 01～4. 0M). Linear plots of φ^(-1) vs. [TEA]^(-1) at low concentration of amine (<0.02M) and Φ^(-1) vs. [TEA]^(-2) at high concentration were obtained. Kinetic data demonstrate that the electron transfer is promoted significantly by DCDAB vesicles and proton transfer becomes more efficient at high Rmlne concentrations, leading to a decrease of Kd/Kr and increase of Kh/Ke. The kinetic expressions of photoreaction of BP bound to DCDAB bilayer are developed.
文摘A series of 2 (E) (4 hydroxy 3 methoxybenzylidene) 5 (N substituted ami nomethyl) cyclopentanones was synthesized and evaluated for the anti inflammatory activity. All of the target compounds were confirmed by spectral analysis and elemental analysis. Preliminary pharmacological tests showed that several compounds exerted appreciable inhibitory effect on xylene induced ear edema in mice and that alteration of the substituents of anilines had significant influence in anti inflammatory potency.
基金supported by the National Natural Science Foundation of China(22225109,92061101,22071109,and 22101089)the Top Youth Project of Guangdong Province Pearl River Talents Program(2021QN02L617)+2 种基金the Excellent Youth Foundation of Jiangsu Provincial Natural Science Foundation(BK20211593)the Open Fund of Energy and Materials Chemistry Joint Laboratory of South China Normal University and Guangzhou Tinci Materials Technology(SCNU-TINCI-202204)Guangdong Provincial Basic and Applied Basic Research Foundation(2023A1515030097 and 2020A1515110836).
文摘The performance applications(e.g.,photocatalysis)of zirconium(Zr)and hafnium(Hf)based complexes are greatly hindered by the limited development of their structures and the relatively inert metal reactivity.In this work,we constructed two ultrastable Zr/Hf-based clusters(Zr_(9)-TC4A and Hf_(9)-TC4A)using hydrophobic 4-tert-butylthiacalix[4]arene(H4TC4A)ligands,in which unsaturated coordinated sulfur(S)atoms on the TC4A^(4-)ligand can generate strong metal–ligand synergy with nearby active metal Zr/Hf sites.As a result,these two functionalized H4TC4A ligands modified Zr/Hf-oxo clusters,as catalysts for the amine oxidation reaction,exhibited excellent catalytic activity,achieving very high substrate conversion(>99%)and product selectivity(>90%).Combining comparative experiments and theoretical calculations,we found that these Zr/Hf-based cluster catalysts accomplish efficient amine oxidation reactions through synergistic effect between metals and ligands:(i)The photocatalytic benzylamine(BA)oxidation reaction was achieved by the synergistic effect of the dual active sites,in which,the naked S sites on the TC4A^(4-)ligand oxidize the BA by photogenerated hole and oxygen molecules are reduced by photogenerated electrons on the metal active sites;(ii)in the aniline oxidation reaction,aniline was adsorbed by the bare S sites on ligands to be closer to metal active sites and then oxidized by the oxygen-containing radicals activated by the metal sites,thus completing the catalytic reaction under the synergistic catalytic effect of the proximity metal–ligand.In this work,the Zr/Hf-based complexes applied in the oxidation of organic amines have been realized using active S atom-directed metal–ligand synergistic catalysis and have demonstrated very high reactivity.
基金supported by the National Natural Science Foundation of China(Nos.21106135 and 51173168)Zhejiang Provincial Key Innovation Team(No.2010R50038)+1 种基金Zhejiang Provincial Top Key Academic Discipline of Chemical Engineering and Technology"521" Talent Project of Zhejiang Sci-Tech University
文摘Under the guidance of the finding that the tyrosine residues in proteins could undergo three-component Mannich-type reactions with formaldehyde and electron-rich aniline-containing compounds,which forms covalent bonding connections between the protein of interest and the aniline with high levels of selectivity under relatively mild conditions,an orange aromatic primary amine-containing acid dye AMODB was designed and readily synthesized.The molecular structure was characterized by FTIR,^1H NMR,mass spectrometry and elemental analysis.The synthesized dye and a similar control dye（C.I.Acid Yellow 11） without primary amine groups were applied to dye silk fabric by three dyeing processes：Mannich-type dyeing（with and without the addition of formaldehyde） and acidic dyeing.Their washing and rubbing fastness properties with different dyeing methods were examined and compared.It was found that the dyed silk fabric with AMODB by the Mannich-type dyeing showed higher color depth,better anti-stripping ability to DMF and better washing fastness than those of the dyed silk fabric with C.I.Acid Yellow 11 by acidic dyeing due to the covalent bond formation between the dye chromophore of AMODB and silk fiber.In addition,mild Mannich dyeing conditions suitable for silk（AMODB at 3%owf,75：1 liquor-to-goods ratio,dyebath pH 5.5,30℃,10 h） were provided.
基金financially supported by the National Natural Science Foundation of China(No.21202116)Independent Innovation Foundation of Tianjin Universityof China(No.2016XZC-0071)Natural Science Foundation of Tianjin of China(No.16JCYBJC20300)
文摘A concise and efficient approach was developed for the synthesis of mono-substituted and di-substituted pyrimidines products via palladium-catalyzed amination of chloro-substituted 5-nitropyrimidines and amines. This synthetic methodology can produce various di-substituted pyrimidines in high yields with good functional group tolerance, and provide a complementary tool for the syntheses of important intermediates of nucleosides and purines with bioactivities.
基金financial support from the National Natural Science Foundation of China (No. 21262022)
文摘An intramolecular organocatalytic enantioselective aza-Michael reaction of carbamates, sulfonamides and acetamides to a,b-unsaturated ketones was developed. This process is promoted by 9-amino-9-deoxy-epi-quinine and diphenyl hydrogen phosphate to afford a straightforward and expeditious synthesis of several synthetically useful five-and six-membered heterocycles with excellent enantioselectivity（92%–97.5% ee） and very good yields（up to 99%）.
