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 kinetics of PTC-Wittig reaction between substituted aromatic aldehydes and 2-butenyl methyldiphenylphosphonium salt has been studied. The low reaction constant (ρ=0. 30) implies that these PTC-Wittig reactions ta...The kinetics of PTC-Wittig reaction between substituted aromatic aldehydes and 2-butenyl methyldiphenylphosphonium salt has been studied. The low reaction constant (ρ=0. 30) implies that these PTC-Wittig reactions take place through low polar intermediate.展开更多
The seleno substituted aromatic compounds were prepared via the Diels-Alder reaction of seleno substituted 3-sulfolenes with dimethyl acetylenedicarboxylate followed by DDQ dehydrogenation.
In the presence of alkali nitrite and carbonate,some nitrobenzenes subs- tituted by strongly electron withdrawing group undergo a self condensation in an aprotic polar sotvent to give symmetrical disubstituted dipheny...In the presence of alkali nitrite and carbonate,some nitrobenzenes subs- tituted by strongly electron withdrawing group undergo a self condensation in an aprotic polar sotvent to give symmetrical disubstituted diphenyl ethers in good yields.A possible mechanism is discussed,the nucteophilic aromatic substitution S_NAr and S_(Ru)Ar may occur simultaneously.展开更多
The cycloaddition reactions between ketene or substituted ketenes and cyelopentadiene have been studied theoretically by means of the semiempirical AMI method.Three different substituted ketenes have been selected and...The cycloaddition reactions between ketene or substituted ketenes and cyelopentadiene have been studied theoretically by means of the semiempirical AMI method.Three different substituted ketenes have been selected and ten transition states,corresponding to different approach geometries have been located and characterized,The regioselectivity and stereoselectivity of the reactions are correctly predicted by the calculations and the reaction mechanisms are analyzed in terms of electronic and steric effects of the substitutents on the reacting ketene and cyc-lopentadiene.展开更多
Conducted in the ionic liquids, activated and inactivated halides, acyl chlorides, tosylate, and bezotriazolyl acylates were converted to corresponding azide and thiocyanide compounds in high yields under mild conditi...Conducted in the ionic liquids, activated and inactivated halides, acyl chlorides, tosylate, and bezotriazolyl acylates were converted to corresponding azide and thiocyanide compounds in high yields under mild conditions.展开更多
α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yiel...α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yield under mild conditions.展开更多
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
Cd, Zn-thionelns were isolated from the rat liver by improved Winge method and purified further. The composition was determined. The mobilization of Cd ions from the Cd, Zn-metallothioneins was studied with spectropho...Cd, Zn-thionelns were isolated from the rat liver by improved Winge method and purified further. The composition was determined. The mobilization of Cd ions from the Cd, Zn-metallothioneins was studied with spectrophotometric method. The results show that the reaction of DTP A or EDTA with Cd, Zn-thioneins occurs through three steps. The first step follows pseudo-first order reaction with association mechanism. The formation constants and the dissociation rate constants of the relevant intermediate ternary complexes and apparent rate constants, Kapp were determined. The properties and structure of Cd, Zn-thioneins and ligands with low molecular weights affect the values of Kapp.展开更多
The title compound FeCo2 (CO)8 (μ3-S) [P (OCH2Ph )3] was synthe-sized by the reaction of P (OCH2Ph)3 with FeCo2 (CO)9 (μ3-S) at room temperature.Crystal data: C29H21 O11 PSCo2Fe, Mr=782. 23, monoclinic, space group ...The title compound FeCo2 (CO)8 (μ3-S) [P (OCH2Ph )3] was synthe-sized by the reaction of P (OCH2Ph)3 with FeCo2 (CO)9 (μ3-S) at room temperature.Crystal data: C29H21 O11 PSCo2Fe, Mr=782. 23, monoclinic, space group P21/n(14), a= l5. 123(4), b=14. 580(4), c=15. 942(3)A, g=115. 66(1), V=3168293K, final R= 0. 032, R= 0. 037 for 3010 observed reflections with I>3. 00(I).The monosubstituted ligand P (OCH2Ph )3 in FeCo2 (CO)8 (μ3-S ) [P (OCH2Ph )3] islinked to one cobalt atom of the tetrahedron FeCo2S framework.展开更多
A new cluster {Mo3S4[NH2CH2CH(O)CH2NH2]3}(DTP)?(H2O)2?(DMF) (DTP = diethyldithiophosphate) has been synthesized via ligand substitution reaction of Mo3S4(DTP)4(H2O) with an alkaline ligand 1,3-diamino-2-propanol(DAPRO...A new cluster {Mo3S4[NH2CH2CH(O)CH2NH2]3}(DTP)?(H2O)2?(DMF) (DTP = diethyldithiophosphate) has been synthesized via ligand substitution reaction of Mo3S4(DTP)4(H2O) with an alkaline ligand 1,3-diamino-2-propanol(DAPROH) in a mixed organic solvent, and its crys- tal structure was determined with the following data: Mo3S6PC16H48O8N7, Mr = 977.76, triclinic, space group P1, Z = 2, a = 10.319(2), b = 12.843(3), c = 15.335(3) ?, α = 65.26(3), β = 82.18(3), γ = 70.67(3)o, V = 1741.7(6) ?3, Dc = 1.864 g/cm3, μ = 1.517 mm-1, F(000) = 988, the final R = 0.0794 and wR = 0.2111 for 6318 observed reflections (I>2σ(I)). The structure analysis indicates that all DTP ligands of Mo3S4(DTP)4(H2O) are replaced and each DAPRO molecule acts as a tri- dentate ligand chelating to each Mo atom of the Mo3S4 core. Different from the precursor, the clus- ter symmetry is elevated to C3. In addition, the UV-spectrum of the title compound was measured.展开更多
A phosphrous-containing poly(aryl ether ketone) was synthesized derived from bisphenol-A and bis[4-(4- fluorobenzoyl)phenyl] phenyl phosphine oxide (FPPPO) by nucleophilic substitution reaction. The structure of...A phosphrous-containing poly(aryl ether ketone) was synthesized derived from bisphenol-A and bis[4-(4- fluorobenzoyl)phenyl] phenyl phosphine oxide (FPPPO) by nucleophilic substitution reaction. The structure of the polymer was characterized by FT-IR, ^1H-NMR and ^31p-NMR. The thermal property of the PAEK was measured by DSC and TGA. The glass transition temperature (Tg) of the polymer was 205℃, and the 5% weight loss temperature under nitrogen was 475℃. Good solubility of the polymer in organic solvents, such as N-methylpyrrolidone, dimethylformamide, dimethylacetamide, dimethylsulfoxide and chloroalkanes was observed, flexible film was obtained from the polymer's CH2Cl2 solution. The limiting oxygen index (LOI) of the PAEK was 40, which indicated that organic phosphorus moiety can offer good flame retardant property to the polymer.展开更多
The negative secondary ion mass spectrometry,in combination with the stereoselective derivatizations with substituted boronic acid RB(OH)_2,was used in the analysis of fourteen oligosac- charides.The mass spectra of t...The negative secondary ion mass spectrometry,in combination with the stereoselective derivatizations with substituted boronic acid RB(OH)_2,was used in the analysis of fourteen oligosac- charides.The mass spectra of the derivatives provide information on their linkage Positions and iso- merism of the individual monoscaccharide units.The results indicated that among the derivatives of the oligosaccharides analyzed,those with 1—4 and 1—6 linkages all presented the ion peaks at m/z 287,sometimes one more peak at m/z 449.Furthermore,a relationship was found between the linkage positions and the intensity orders of the derivative ions.Finally,the derivatives of the disaccharides with a galactose presented an intense ion peak at m/z 347,and those of oligosaccharides with 1—6 linkage to a galactose at terminal presented the ion at m/z 317.In the case of oligosaccharides with a fructose residue,characteristic ion of m/z 155 was produced.The conditions of stereoselective derivatizations and mass spectrometry were studied,in order to obtain a better reproducibility of the mass spectra.展开更多
For the isomerization reaction of monofluoro-disilene,the geometrical structures of reac- tant,product and transition state have been optimized and energy constant,vibrational frequency calculated.By means of the stat...For the isomerization reaction of monofluoro-disilene,the geometrical structures of reac- tant,product and transition state have been optimized and energy constant,vibrational frequency calculated.By means of the statistical thermodynamics and Eyring's transition state theory,the equilibrium constant,rate constant and heat of isomerization have also been computed.Hence, this reaction has been analysed completely.展开更多
Eight new complexes with the formula [PhC_2C(OH)R^2R^2]Co_2(CO)_6 were prepared from phenyl substituted propargylic alcohols and dicobalt octacarbonyl.The reactions of these propargylio alcohol complexes with active m...Eight new complexes with the formula [PhC_2C(OH)R^2R^2]Co_2(CO)_6 were prepared from phenyl substituted propargylic alcohols and dicobalt octacarbonyl.The reactions of these propargylio alcohol complexes with active methylene compounds,2,4-pentanedione or ethyl acetoacetate,in the presnce of an acid,HBF_4(40%)+P_2O_5(in excess)or BF_3·Et_2O,at room temperature in dichlorome- thane were investigated.From the 1-alkyl substituted tertiary propargylic alcohol complexes,three new conjugated ene-yne complexes produced by intramolecular dehydration reaction were isolated in high yields(82—95%).On the other hand,four new alkylated complexes were obtained with satisfactory yields(44—66%)from the secondary propargylic alcohol complexes.The influence of other acids,phosphorus pentoxide and polyphosphoric acid,on both dehydration reaction and alkylated reaction was also studied.展开更多
Cross-linked poly(diallyldimethylammonium chloride) and its derivative copolymers were synthesized and used as phase transfer catalyst in the nucleophilic substitution reaction especially halogen exchange reactions....Cross-linked poly(diallyldimethylammonium chloride) and its derivative copolymers were synthesized and used as phase transfer catalyst in the nucleophilic substitution reaction especially halogen exchange reactions.In addition,the effect of hydrophilic-hydrophobic character of the polymers in the nucleophilic reactions was investigated.展开更多
In this paper, the activities of electrophilic sites on benzene ring of 4-substituted anilines and their acyl compounds were studied with the quantitative indicator of multiphilicity descriptor. Four substituents were...In this paper, the activities of electrophilic sites on benzene ring of 4-substituted anilines and their acyl compounds were studied with the quantitative indicator of multiphilicity descriptor. Four substituents were synthe- sized with microwave irradiation in good yields to verify the quantitative analysis data. Friedel-Crafts acylation was carried out by the microwave method for the first time.展开更多
Defect states in perovskite films restrict the interfacial stability and open-circuit voltage of perovskite solar cells.Here,aiming at superior interfacial passivation,we investigate the reconfiguration of perovskite ...Defect states in perovskite films restrict the interfacial stability and open-circuit voltage of perovskite solar cells.Here,aiming at superior interfacial passivation,we investigate the reconfiguration of perovskite interface by the interaction between a series of quaternary ammonium bromides(QAB)and lead—halide(Pb—X)octahedrons.Bromide—iodide substitution reaction or R4NBr addition reaction may occur on the perovskite surface,which is related to the steric hindrance of quaternary ammonium cations.On this basis,the perovskite surface morphology,band structure,growth orientation and defect states are reconstructed via the R4NBr addition reaction.This ordered lead—halide adduct could effectively repair the imperfect perovskite/hole transportation layer interface to suppress non-radiative recombination and ion migration toward ultralong carrier lifetime surpassing 10µs.The resulting perovskite solar cells yield the efficiency of 23.89%with steady-state efficiency of 23.70%.The passivated cells can sustain 86%of initial efficiency after 200-h operation,which is attributed to the passivation effect and hydrophobic characteristics.This work provides an avenue for reconfiguring perovskite surface by QABs.展开更多
A rather satisfactory method of synthesis of aldoximes and ketoximes by direct nitrosation of alkanes and an adequate technique of separating the mixtures and identifying the components from the reactions were worked ...A rather satisfactory method of synthesis of aldoximes and ketoximes by direct nitrosation of alkanes and an adequate technique of separating the mixtures and identifying the components from the reactions were worked out.By these procedures, the nitrosation of pentane, hexane and heptane gave different results from those reported in literature, and the study on octane was new.展开更多
A new class of rhodium complexes with high catalytic activity as well as excellent stability, which was used as catalyst for carbonylation of methanol to acetic acid, is reported. It contains free donor (namely un-coo...A new class of rhodium complexes with high catalytic activity as well as excellent stability, which was used as catalyst for carbonylation of methanol to acetic acid, is reported. It contains free donor (namely un-coordinated donor) atoms which enable to improve its stability by intramolecular substitution reaction. Its synthesis, characteristic and catalytic reaction were discussed here.展开更多
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 kinetics of PTC-Wittig reaction between substituted aromatic aldehydes and 2-butenyl methyldiphenylphosphonium salt has been studied. The low reaction constant (ρ=0. 30) implies that these PTC-Wittig reactions take place through low polar intermediate.
文摘The seleno substituted aromatic compounds were prepared via the Diels-Alder reaction of seleno substituted 3-sulfolenes with dimethyl acetylenedicarboxylate followed by DDQ dehydrogenation.
基金Supported by the Education Department of Ministry of Metatturgical Industry of PRC.
文摘In the presence of alkali nitrite and carbonate,some nitrobenzenes subs- tituted by strongly electron withdrawing group undergo a self condensation in an aprotic polar sotvent to give symmetrical disubstituted diphenyl ethers in good yields.A possible mechanism is discussed,the nucteophilic aromatic substitution S_NAr and S_(Ru)Ar may occur simultaneously.
文摘The cycloaddition reactions between ketene or substituted ketenes and cyelopentadiene have been studied theoretically by means of the semiempirical AMI method.Three different substituted ketenes have been selected and ten transition states,corresponding to different approach geometries have been located and characterized,The regioselectivity and stereoselectivity of the reactions are correctly predicted by the calculations and the reaction mechanisms are analyzed in terms of electronic and steric effects of the substitutents on the reacting ketene and cyc-lopentadiene.
文摘Conducted in the ionic liquids, activated and inactivated halides, acyl chlorides, tosylate, and bezotriazolyl acylates were converted to corresponding azide and thiocyanide compounds in high yields under mild conditions.
文摘α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yield under mild conditions.
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.
基金This study was supported by National Natural Science Foundation of China.
文摘Cd, Zn-thionelns were isolated from the rat liver by improved Winge method and purified further. The composition was determined. The mobilization of Cd ions from the Cd, Zn-metallothioneins was studied with spectrophotometric method. The results show that the reaction of DTP A or EDTA with Cd, Zn-thioneins occurs through three steps. The first step follows pseudo-first order reaction with association mechanism. The formation constants and the dissociation rate constants of the relevant intermediate ternary complexes and apparent rate constants, Kapp were determined. The properties and structure of Cd, Zn-thioneins and ligands with low molecular weights affect the values of Kapp.
文摘The title compound FeCo2 (CO)8 (μ3-S) [P (OCH2Ph )3] was synthe-sized by the reaction of P (OCH2Ph)3 with FeCo2 (CO)9 (μ3-S) at room temperature.Crystal data: C29H21 O11 PSCo2Fe, Mr=782. 23, monoclinic, space group P21/n(14), a= l5. 123(4), b=14. 580(4), c=15. 942(3)A, g=115. 66(1), V=3168293K, final R= 0. 032, R= 0. 037 for 3010 observed reflections with I>3. 00(I).The monosubstituted ligand P (OCH2Ph )3 in FeCo2 (CO)8 (μ3-S ) [P (OCH2Ph )3] islinked to one cobalt atom of the tetrahedron FeCo2S framework.
基金This work was supported by the State Key Basic Research and Development Plan of China (001CB108906)the NNSF of China (20173063) NSF of Fujian Province (E0020001)
文摘A new cluster {Mo3S4[NH2CH2CH(O)CH2NH2]3}(DTP)?(H2O)2?(DMF) (DTP = diethyldithiophosphate) has been synthesized via ligand substitution reaction of Mo3S4(DTP)4(H2O) with an alkaline ligand 1,3-diamino-2-propanol(DAPROH) in a mixed organic solvent, and its crys- tal structure was determined with the following data: Mo3S6PC16H48O8N7, Mr = 977.76, triclinic, space group P1, Z = 2, a = 10.319(2), b = 12.843(3), c = 15.335(3) ?, α = 65.26(3), β = 82.18(3), γ = 70.67(3)o, V = 1741.7(6) ?3, Dc = 1.864 g/cm3, μ = 1.517 mm-1, F(000) = 988, the final R = 0.0794 and wR = 0.2111 for 6318 observed reflections (I>2σ(I)). The structure analysis indicates that all DTP ligands of Mo3S4(DTP)4(H2O) are replaced and each DAPRO molecule acts as a tri- dentate ligand chelating to each Mo atom of the Mo3S4 core. Different from the precursor, the clus- ter symmetry is elevated to C3. In addition, the UV-spectrum of the title compound was measured.
基金This work was supported by the National Natural Science Foundation of China(No.50203008).
文摘A phosphrous-containing poly(aryl ether ketone) was synthesized derived from bisphenol-A and bis[4-(4- fluorobenzoyl)phenyl] phenyl phosphine oxide (FPPPO) by nucleophilic substitution reaction. The structure of the polymer was characterized by FT-IR, ^1H-NMR and ^31p-NMR. The thermal property of the PAEK was measured by DSC and TGA. The glass transition temperature (Tg) of the polymer was 205℃, and the 5% weight loss temperature under nitrogen was 475℃. Good solubility of the polymer in organic solvents, such as N-methylpyrrolidone, dimethylformamide, dimethylacetamide, dimethylsulfoxide and chloroalkanes was observed, flexible film was obtained from the polymer's CH2Cl2 solution. The limiting oxygen index (LOI) of the PAEK was 40, which indicated that organic phosphorus moiety can offer good flame retardant property to the polymer.
基金Project supported by the National Natural Science Foundation of China
文摘The negative secondary ion mass spectrometry,in combination with the stereoselective derivatizations with substituted boronic acid RB(OH)_2,was used in the analysis of fourteen oligosac- charides.The mass spectra of the derivatives provide information on their linkage Positions and iso- merism of the individual monoscaccharide units.The results indicated that among the derivatives of the oligosaccharides analyzed,those with 1—4 and 1—6 linkages all presented the ion peaks at m/z 287,sometimes one more peak at m/z 449.Furthermore,a relationship was found between the linkage positions and the intensity orders of the derivative ions.Finally,the derivatives of the disaccharides with a galactose presented an intense ion peak at m/z 347,and those of oligosaccharides with 1—6 linkage to a galactose at terminal presented the ion at m/z 317.In the case of oligosaccharides with a fructose residue,characteristic ion of m/z 155 was produced.The conditions of stereoselective derivatizations and mass spectrometry were studied,in order to obtain a better reproducibility of the mass spectra.
基金This research was supported by the National Natural Science Foundation of China.
文摘For the isomerization reaction of monofluoro-disilene,the geometrical structures of reac- tant,product and transition state have been optimized and energy constant,vibrational frequency calculated.By means of the statistical thermodynamics and Eyring's transition state theory,the equilibrium constant,rate constant and heat of isomerization have also been computed.Hence, this reaction has been analysed completely.
基金Work supported by the National Natural Science Foundation of China.
文摘Eight new complexes with the formula [PhC_2C(OH)R^2R^2]Co_2(CO)_6 were prepared from phenyl substituted propargylic alcohols and dicobalt octacarbonyl.The reactions of these propargylio alcohol complexes with active methylene compounds,2,4-pentanedione or ethyl acetoacetate,in the presnce of an acid,HBF_4(40%)+P_2O_5(in excess)or BF_3·Et_2O,at room temperature in dichlorome- thane were investigated.From the 1-alkyl substituted tertiary propargylic alcohol complexes,three new conjugated ene-yne complexes produced by intramolecular dehydration reaction were isolated in high yields(82—95%).On the other hand,four new alkylated complexes were obtained with satisfactory yields(44—66%)from the secondary propargylic alcohol complexes.The influence of other acids,phosphorus pentoxide and polyphosphoric acid,on both dehydration reaction and alkylated reaction was also studied.
文摘Cross-linked poly(diallyldimethylammonium chloride) and its derivative copolymers were synthesized and used as phase transfer catalyst in the nucleophilic substitution reaction especially halogen exchange reactions.In addition,the effect of hydrophilic-hydrophobic character of the polymers in the nucleophilic reactions was investigated.
文摘In this paper, the activities of electrophilic sites on benzene ring of 4-substituted anilines and their acyl compounds were studied with the quantitative indicator of multiphilicity descriptor. Four substituents were synthe- sized with microwave irradiation in good yields to verify the quantitative analysis data. Friedel-Crafts acylation was carried out by the microwave method for the first time.
基金supported by the National Natural Science Foundation of China (51872321, 11874402, 52172260, 52072402,52102332 and 52102267)Ministry of Sciecnce and Technology of the People’s Republic of China (2021YFB3800103)the Fundamental Research Fund for the Central University,Nankai University (023/63213101)。
文摘Defect states in perovskite films restrict the interfacial stability and open-circuit voltage of perovskite solar cells.Here,aiming at superior interfacial passivation,we investigate the reconfiguration of perovskite interface by the interaction between a series of quaternary ammonium bromides(QAB)and lead—halide(Pb—X)octahedrons.Bromide—iodide substitution reaction or R4NBr addition reaction may occur on the perovskite surface,which is related to the steric hindrance of quaternary ammonium cations.On this basis,the perovskite surface morphology,band structure,growth orientation and defect states are reconstructed via the R4NBr addition reaction.This ordered lead—halide adduct could effectively repair the imperfect perovskite/hole transportation layer interface to suppress non-radiative recombination and ion migration toward ultralong carrier lifetime surpassing 10µs.The resulting perovskite solar cells yield the efficiency of 23.89%with steady-state efficiency of 23.70%.The passivated cells can sustain 86%of initial efficiency after 200-h operation,which is attributed to the passivation effect and hydrophobic characteristics.This work provides an avenue for reconfiguring perovskite surface by QABs.
文摘A rather satisfactory method of synthesis of aldoximes and ketoximes by direct nitrosation of alkanes and an adequate technique of separating the mixtures and identifying the components from the reactions were worked out.By these procedures, the nitrosation of pentane, hexane and heptane gave different results from those reported in literature, and the study on octane was new.
基金Project (No. 29974035) supported by the National Natural Science Foundation of China
文摘A new class of rhodium complexes with high catalytic activity as well as excellent stability, which was used as catalyst for carbonylation of methanol to acetic acid, is reported. It contains free donor (namely un-coordinated donor) atoms which enable to improve its stability by intramolecular substitution reaction. Its synthesis, characteristic and catalytic reaction were discussed here.