Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichlo...Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichloroethane and tris(2-chloroethyl)amine, respectively in dimethyl formamide in the presence of anhydrous potassium carbonate. The crystal data are: monoclinic, P21/c, a = 7.571(2), b = 12.608(3), c = 7.357(2) ? b = 105.823(6)? V = 675.7(2) 3, Mr = 270.3, Z = 2, Dc = 1.328 g/cm3, F(000) = 284, m(MoKa) = 0.096 mm-1, R = 0.0537 and wR = 0.2189 for compound 1; and monoclinic, P21/n, a = 11.7162(6), b = 9.0042(6), c = 22.908(2) ? b = 99.505(1)? V = 2383.5(3) ?, Mr = 461.50, Z = 4, Dc = 1.286 g/cm3, F(000)= 976, m(MoKa) = 0.091 mm-1, R = 0.0464 and wR = 0.1462 for compound 2. The molecule of compound 1 (dialdehyde) is located at the crystallographic inversion center nearby the midpoint of C(8)C(8A) single bond. The three chains in the molecule of compound 2 (trialdehyde) are of non-crystallographic pseudo-C3 symmetry, and each of them is quite planar.展开更多
Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge.Herein,we report the immobilization of TsDPEN on SBA‐15 with...Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge.Herein,we report the immobilization of TsDPEN on SBA‐15 with an ionic liquid(IL)linkage via the one‐pot reaction of imidazole‐TsDPEN‐N‐Boc with 3‐(trimethoxysilyl)propyl bromide in the SBA‐15 mesopores.After coordination to Rh,the chiral solid catalysts could efficiently catalyze quinoline transfer hydrogenation,achieving 97%conversion with 93%ee,which was comparable to their homogeneous counterparts.The chiral solid catalyst with the IL linkage afforded much higher turnover frequency than that without the IL linkage(93 h^(–1)vs.33 h^(–1)),attributed to the phase transfer and formate‐enriching ability of the IL linkage.Furthermore,the effect of the pH on the reaction rate of the solid catalyst was investigated,preventing reaction rate retardation during the catalytic process.The tuning of the linkage group is an efficient approach for catalytic activity improvement of immobilized chiral catalysts.展开更多
Case 1: Mr. Li, a 55-year farmer from Hebeiprovince, paid his first visit on August 11, 1995. Thepatient complained of a sudden pain in the area fromhis left buttock down to the posterolateral aspect ofthe leg.
Acetyl crosslinked polystyrene (EPS) and crosslinked bromoacetyl polystyrene (BEPS)beads were synthesized by Fridel-Crafts acetylation of polystyrene (PS) and bromination of EPS respectively. FTIR, XPS, and TG-TDG wer...Acetyl crosslinked polystyrene (EPS) and crosslinked bromoacetyl polystyrene (BEPS)beads were synthesized by Fridel-Crafts acetylation of polystyrene (PS) and bromination of EPS respectively. FTIR, XPS, and TG-TDG were employed to characterize their structures. The results revealed there are two types of bromine in the BEPS molecule. One is in the main chain of polystyrene and the other is in the acetyl. The results of TG-DTG showed that the rates of loss weight of PS, EPS, and BEPS were 92.7%, 92.2%, and 81.3% among the 300 ℃～500 ℃; 7.3%, 7.8%, and 18. 7% in 594 ℃, 660 ℃, and 584.8 ℃, respectively.展开更多
The crystal and molecular structure of diethyl l-(p-toluenesulfon-amido ) - p chlofoPhenylmet hylphosphonate has been determined by X- ray d iffractionmethod- The crystal (C18,H23,ClNO5PS) is monoclinic with space gro...The crystal and molecular structure of diethyl l-(p-toluenesulfon-amido ) - p chlofoPhenylmet hylphosphonate has been determined by X- ray d iffractionmethod- The crystal (C18,H23,ClNO5PS) is monoclinic with space group P21/c, a =8. 162(6), b= l8. O64(7), c= l4. 362(4) A, β=96. 29(3)°, V=2lO4. 7 A3, M.=431, 88, Z=4, Dx= l. 364 g/cm3, μ, = 3. 765 cm-1, F(000) = 904, R=0. 047 andRw=0. 0049 for 998 reflections with I>3σ(I). The 1H NMR spetrum of the title com-pound shows that the two ethoxy groups are magnetic nonequivalent, which is in agree-ment with its X-ray analysis result-展开更多
A group of grafted PET fibers with different graft yield are formed by grafting acrylamide onto the PET main chains. The structure of grafted fibers are studied by scanning electronic microscope ( SEM ), infra-red spe...A group of grafted PET fibers with different graft yield are formed by grafting acrylamide onto the PET main chains. The structure of grafted fibers are studied by scanning electronic microscope ( SEM ), infra-red spectrophotometer ( IR ), and differential scanning calorimetry(DSC). At the same time, the moisture regain, dyeability, strength, and elongation at break of the samples are measured and their relations with structural changes are discussed. Compared with ungrafted fiber, shape of the fiber cross-section, IR characteristic absorption peaks, and melting behavior of the grafted fibers have been changed, causing the fiber dyeability and moisture regain to be increased, and mechanical properties to be changed.展开更多
A microporous luminescent metal-organic framework [Zn4L2（H2O）2]＇（H2O）m（DMA）n （1） （H4L=5,5＇-（（1H-pyrazole-3,5-di- carbonyl）bis（azanediyl））diisophthalic acid, DMA=N,N-dimethylacetamide） was synthesized...A microporous luminescent metal-organic framework [Zn4L2（H2O）2]＇（H2O）m（DMA）n （1） （H4L=5,5＇-（（1H-pyrazole-3,5-di- carbonyl）bis（azanediyl））diisophthalic acid, DMA=N,N-dimethylacetamide） was synthesized and characterized by infrared ra- diation （IR）, thermogravimetric analyses （TGA）, powder X-ray diffraction spectra （PXRD） and X-ray diffraction. Complex 1 has a three dimensional （3D） framework, which can be simplified as 5,5,5,5-c net with the Schlafi symbol of {43.64.83} {44.65.8 } {45.65 }2. This luminescent metal-organic framework （MOF） shows selectively sensitive to nitrobenzene and series of nitroaromatic explosives such as 4-nitrotoluene, 1,4-dinitrobenzene, 1,3-dinitrobenzene and 2,4-dinitrotoluene, and exhibits well recyclability. So complex 1 could be used to detect nitroaromatic explosives as a selective sensing material.展开更多
Various polysulfonamide （PSA） statistical copolymers were synthesized by polycondensation of three aromatic diamines and terephthaloyl chloride. The inherent viscosities of the resulting PSA copolymers range from 1....Various polysulfonamide （PSA） statistical copolymers were synthesized by polycondensation of three aromatic diamines and terephthaloyl chloride. The inherent viscosities of the resulting PSA copolymers range from 1.54 to 1.66 dL/g. The precipitated PSA copolymers with feed content of p-phenylene diamine （PPD） being less than 50% （mole fraction） can be redissolved in N-methyl-2-pryrrolidone （NMP） or N, N-dimethylacetamide （DMAc） with lithium chloride of WLiC1 ： 0.02. All of the PSA copolymers exhibit enhanced tensile strength in comparison with PSA and still maintain excellent thermal stability in either air or nitrogen atmosphere展开更多
基金The authors thank the financial support of the Natural Science Foundation of Fujian Province (No. E0110010)
文摘Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichloroethane and tris(2-chloroethyl)amine, respectively in dimethyl formamide in the presence of anhydrous potassium carbonate. The crystal data are: monoclinic, P21/c, a = 7.571(2), b = 12.608(3), c = 7.357(2) ? b = 105.823(6)? V = 675.7(2) 3, Mr = 270.3, Z = 2, Dc = 1.328 g/cm3, F(000) = 284, m(MoKa) = 0.096 mm-1, R = 0.0537 and wR = 0.2189 for compound 1; and monoclinic, P21/n, a = 11.7162(6), b = 9.0042(6), c = 22.908(2) ? b = 99.505(1)? V = 2383.5(3) ?, Mr = 461.50, Z = 4, Dc = 1.286 g/cm3, F(000)= 976, m(MoKa) = 0.091 mm-1, R = 0.0464 and wR = 0.1462 for compound 2. The molecule of compound 1 (dialdehyde) is located at the crystallographic inversion center nearby the midpoint of C(8)C(8A) single bond. The three chains in the molecule of compound 2 (trialdehyde) are of non-crystallographic pseudo-C3 symmetry, and each of them is quite planar.
文摘Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge.Herein,we report the immobilization of TsDPEN on SBA‐15 with an ionic liquid(IL)linkage via the one‐pot reaction of imidazole‐TsDPEN‐N‐Boc with 3‐(trimethoxysilyl)propyl bromide in the SBA‐15 mesopores.After coordination to Rh,the chiral solid catalysts could efficiently catalyze quinoline transfer hydrogenation,achieving 97%conversion with 93%ee,which was comparable to their homogeneous counterparts.The chiral solid catalyst with the IL linkage afforded much higher turnover frequency than that without the IL linkage(93 h^(–1)vs.33 h^(–1)),attributed to the phase transfer and formate‐enriching ability of the IL linkage.Furthermore,the effect of the pH on the reaction rate of the solid catalyst was investigated,preventing reaction rate retardation during the catalytic process.The tuning of the linkage group is an efficient approach for catalytic activity improvement of immobilized chiral catalysts.
文摘Case 1: Mr. Li, a 55-year farmer from Hebeiprovince, paid his first visit on August 11, 1995. Thepatient complained of a sudden pain in the area fromhis left buttock down to the posterolateral aspect ofthe leg.
基金National Natural Science Foundation of China (No.29906008) and Nature Science Foundation of Shandong Province (No.Q99B15).
文摘Acetyl crosslinked polystyrene (EPS) and crosslinked bromoacetyl polystyrene (BEPS)beads were synthesized by Fridel-Crafts acetylation of polystyrene (PS) and bromination of EPS respectively. FTIR, XPS, and TG-TDG were employed to characterize their structures. The results revealed there are two types of bromine in the BEPS molecule. One is in the main chain of polystyrene and the other is in the acetyl. The results of TG-DTG showed that the rates of loss weight of PS, EPS, and BEPS were 92.7%, 92.2%, and 81.3% among the 300 ℃～500 ℃; 7.3%, 7.8%, and 18. 7% in 594 ℃, 660 ℃, and 584.8 ℃, respectively.
文摘The crystal and molecular structure of diethyl l-(p-toluenesulfon-amido ) - p chlofoPhenylmet hylphosphonate has been determined by X- ray d iffractionmethod- The crystal (C18,H23,ClNO5PS) is monoclinic with space group P21/c, a =8. 162(6), b= l8. O64(7), c= l4. 362(4) A, β=96. 29(3)°, V=2lO4. 7 A3, M.=431, 88, Z=4, Dx= l. 364 g/cm3, μ, = 3. 765 cm-1, F(000) = 904, R=0. 047 andRw=0. 0049 for 998 reflections with I>3σ(I). The 1H NMR spetrum of the title com-pound shows that the two ethoxy groups are magnetic nonequivalent, which is in agree-ment with its X-ray analysis result-
文摘A group of grafted PET fibers with different graft yield are formed by grafting acrylamide onto the PET main chains. The structure of grafted fibers are studied by scanning electronic microscope ( SEM ), infra-red spectrophotometer ( IR ), and differential scanning calorimetry(DSC). At the same time, the moisture regain, dyeability, strength, and elongation at break of the samples are measured and their relations with structural changes are discussed. Compared with ungrafted fiber, shape of the fiber cross-section, IR characteristic absorption peaks, and melting behavior of the grafted fibers have been changed, causing the fiber dyeability and moisture regain to be increased, and mechanical properties to be changed.
基金supported by the National Basic Research Program of China (2014CB845600)the National Natural Science of Foundation of China (21371102, 21421001)+1 种基金the MOE Innovation Team of China (IRT13022)the China Postdoctoral Science Foundation funded project (2015M571260)
文摘A microporous luminescent metal-organic framework [Zn4L2（H2O）2]＇（H2O）m（DMA）n （1） （H4L=5,5＇-（（1H-pyrazole-3,5-di- carbonyl）bis（azanediyl））diisophthalic acid, DMA=N,N-dimethylacetamide） was synthesized and characterized by infrared ra- diation （IR）, thermogravimetric analyses （TGA）, powder X-ray diffraction spectra （PXRD） and X-ray diffraction. Complex 1 has a three dimensional （3D） framework, which can be simplified as 5,5,5,5-c net with the Schlafi symbol of {43.64.83} {44.65.8 } {45.65 }2. This luminescent metal-organic framework （MOF） shows selectively sensitive to nitrobenzene and series of nitroaromatic explosives such as 4-nitrotoluene, 1,4-dinitrobenzene, 1,3-dinitrobenzene and 2,4-dinitrotoluene, and exhibits well recyclability. So complex 1 could be used to detect nitroaromatic explosives as a selective sensing material.
基金the National Natural Science Foundation of China (No. 50973059)the Scientific Research Foundation of 2009 Graduate School of Shanghai University
文摘Various polysulfonamide （PSA） statistical copolymers were synthesized by polycondensation of three aromatic diamines and terephthaloyl chloride. The inherent viscosities of the resulting PSA copolymers range from 1.54 to 1.66 dL/g. The precipitated PSA copolymers with feed content of p-phenylene diamine （PPD） being less than 50% （mole fraction） can be redissolved in N-methyl-2-pryrrolidone （NMP） or N, N-dimethylacetamide （DMAc） with lithium chloride of WLiC1 ： 0.02. All of the PSA copolymers exhibit enhanced tensile strength in comparison with PSA and still maintain excellent thermal stability in either air or nitrogen atmosphere
