A series of 2-phenyliminothiazolidines has been successfully synthesized; and 2-(2-methylphenyl)iminothiazolidine(Ⅰa) and 2-(4-methylphenyl) iminothiazolidine(Ⅰb) have been selected to determine their crystal struct...A series of 2-phenyliminothiazolidines has been successfully synthesized; and 2-(2-methylphenyl)iminothiazolidine(Ⅰa) and 2-(4-methylphenyl) iminothiazolidine(Ⅰb) have been selected to determine their crystal structures by X-ray diffraction technique, from their molecular graph of it is shown that double bond at 2-carbon atom of the heterocycle is all extro-cyclic at the crystal state, and there are two main plaines in Ⅰa and Ⅰb . But in Ⅰa , the angle between the planes is 61.4° and in Ⅰb the angle is about 41.4°. And so there is a strong conjugative effect in Ⅰb than in Ⅰa. So it is thought that the difference in fungicidal activies between 2-substitutedphenyl compounds(Ⅰa) and 4-substitutedphenyl compounds(Ⅰb) is due to their space factors.展开更多
Poly(p-phenylene terephthalamide)(PPTA)pulp was prepared by polycondensation of the p-phenylene diamine(PPDA)with terephthaloyl chloride(TPC)in the completely anhydrous solvent system of N-methyl pyrrolidone(NMP)havin...Poly(p-phenylene terephthalamide)(PPTA)pulp was prepared by polycondensation of the p-phenylene diamine(PPDA)with terephthaloyl chloride(TPC)in the completely anhydrous solvent system of N-methyl pyrrolidone(NMP)having calcium chloride,in the presence of poly(vinyl pyrrolidone)(PVP)having a viscosity average molecular weight lower than 40 000.It was confirmed that the polycondensation could be accelerated,the inherent viscosity of the polymer could be increased,and the polymers could be fibrillated more easily by the addition of the PVP.FTIR and X-ray spectra proved that PVP had not combined into molecular chains of the resultant PPTA pulps.The morphology of the resultant pulps,the effect of viscosity average molecular weight,amount and adding mode of PVP on inherent viscosity,specific surface area,and mean length of the resultant pulps were discussed in detail.And the friction and wear properties of the compound reinforced by the resultant pulps were simply investigated.展开更多
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
N-(5-phenylseleno)pentyl succinimide 1, C15H19NO2Se (Mr = 324.27), was prepared by treating Br(CH2)5SePh with potassium succinimide. Its crystal structure has been determined by X-ray single-crystal diffraction. The c...N-(5-phenylseleno)pentyl succinimide 1, C15H19NO2Se (Mr = 324.27), was prepared by treating Br(CH2)5SePh with potassium succinimide. Its crystal structure has been determined by X-ray single-crystal diffraction. The crystal of 1 belongs to monoclinic system, space group P21/c with the crystal cell parameters: a = 18.018(6), b = 5.980(2), c = 14.682(5) ? = 109.977(6)? V = 1486.7(9) 3, Z = 4, Dc = 1.449 g/cm3, (MoK? = 2.523 mm-1, F(000) = 664,the final R = 0.0302 and wR = 0.0666 for 2623 independent observed reflections with I > 2(I). Structure analyses revealed that there exist strong nonclassical hydrogen bonds (CH…O).展开更多
It is investigated the interaction of Ge（IV） with bis（2,3,4-trigodroksifenolazo） benzidine （R） in the presence of KSAS （cationic surface active substances）-CPCl （cetylpyridinium chloride）, CPBr （cetylpyridi...It is investigated the interaction of Ge（IV） with bis（2,3,4-trigodroksifenolazo） benzidine （R） in the presence of KSAS （cationic surface active substances）-CPCl （cetylpyridinium chloride）, CPBr （cetylpyridinium bromide） and CTMABr （cetyltrimethylammonium bromide）. It is studied the effect pH, time on the formation of ternary complexes. It is determinated of molar absorption coefficients and stability constants of germanium. Binary （Ge-R） and triple （Ge-R-CPCI, Ge-R-CPBr, Ge-R-CTMaBr） complex form at pH 4 and pH 1, respectively. The composition proportion of binar system is 1：2 and the composition proportion triple complex is 1：1：2. The concentration interval of germanium which obeying beer low in the Ge-R 0.12-2.92 mkq/mL, in the Ge-R-CPCI is 0.04-1.46 mkq/mL, in the Ge-R-CPBr is 0.00-1.00 mkq/mL and in the Ge-R-CTMaBr is 0.00-1.00 mkq/mL. Molar absorbtivities of complexes are 45,000, 57,000, 59,000 and 60,000, respectively. The effect of interfering ions and masking agents has been learned. Stability constants of complexes have been determined： lgKl = 7.21 ＋ 0.06 （Ge-R）,＇ lgK1 = 12.08 _＋ 0.05 （Ge-R-CPCI）, lgK1 = 12.12 ＋ 0.07 （Ge-R-CPBr） and lgK1 = 12.85 ＋ 0.06 （Ge-R-CTMaBr）. It is developed highly selective method of photometric determination of trace amounts of Ge（IV） in petroleum coke.展开更多
文摘A series of 2-phenyliminothiazolidines has been successfully synthesized; and 2-(2-methylphenyl)iminothiazolidine(Ⅰa) and 2-(4-methylphenyl) iminothiazolidine(Ⅰb) have been selected to determine their crystal structures by X-ray diffraction technique, from their molecular graph of it is shown that double bond at 2-carbon atom of the heterocycle is all extro-cyclic at the crystal state, and there are two main plaines in Ⅰa and Ⅰb . But in Ⅰa , the angle between the planes is 61.4° and in Ⅰb the angle is about 41.4°. And so there is a strong conjugative effect in Ⅰb than in Ⅰa. So it is thought that the difference in fungicidal activies between 2-substitutedphenyl compounds(Ⅰa) and 4-substitutedphenyl compounds(Ⅰb) is due to their space factors.
文摘Poly(p-phenylene terephthalamide)(PPTA)pulp was prepared by polycondensation of the p-phenylene diamine(PPDA)with terephthaloyl chloride(TPC)in the completely anhydrous solvent system of N-methyl pyrrolidone(NMP)having calcium chloride,in the presence of poly(vinyl pyrrolidone)(PVP)having a viscosity average molecular weight lower than 40 000.It was confirmed that the polycondensation could be accelerated,the inherent viscosity of the polymer could be increased,and the polymers could be fibrillated more easily by the addition of the PVP.FTIR and X-ray spectra proved that PVP had not combined into molecular chains of the resultant PPTA pulps.The morphology of the resultant pulps,the effect of viscosity average molecular weight,amount and adding mode of PVP on inherent viscosity,specific surface area,and mean length of the resultant pulps were discussed in detail.And the friction and wear properties of the compound reinforced by the resultant pulps were simply investigated.
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.
基金This work was supported by the NNSFC (No. 29832030)
文摘N-(5-phenylseleno)pentyl succinimide 1, C15H19NO2Se (Mr = 324.27), was prepared by treating Br(CH2)5SePh with potassium succinimide. Its crystal structure has been determined by X-ray single-crystal diffraction. The crystal of 1 belongs to monoclinic system, space group P21/c with the crystal cell parameters: a = 18.018(6), b = 5.980(2), c = 14.682(5) ? = 109.977(6)? V = 1486.7(9) 3, Z = 4, Dc = 1.449 g/cm3, (MoK? = 2.523 mm-1, F(000) = 664,the final R = 0.0302 and wR = 0.0666 for 2623 independent observed reflections with I > 2(I). Structure analyses revealed that there exist strong nonclassical hydrogen bonds (CH…O).
文摘It is investigated the interaction of Ge（IV） with bis（2,3,4-trigodroksifenolazo） benzidine （R） in the presence of KSAS （cationic surface active substances）-CPCl （cetylpyridinium chloride）, CPBr （cetylpyridinium bromide） and CTMABr （cetyltrimethylammonium bromide）. It is studied the effect pH, time on the formation of ternary complexes. It is determinated of molar absorption coefficients and stability constants of germanium. Binary （Ge-R） and triple （Ge-R-CPCI, Ge-R-CPBr, Ge-R-CTMaBr） complex form at pH 4 and pH 1, respectively. The composition proportion of binar system is 1：2 and the composition proportion triple complex is 1：1：2. The concentration interval of germanium which obeying beer low in the Ge-R 0.12-2.92 mkq/mL, in the Ge-R-CPCI is 0.04-1.46 mkq/mL, in the Ge-R-CPBr is 0.00-1.00 mkq/mL and in the Ge-R-CTMaBr is 0.00-1.00 mkq/mL. Molar absorbtivities of complexes are 45,000, 57,000, 59,000 and 60,000, respectively. The effect of interfering ions and masking agents has been learned. Stability constants of complexes have been determined： lgKl = 7.21 ＋ 0.06 （Ge-R）,＇ lgK1 = 12.08 _＋ 0.05 （Ge-R-CPCI）, lgK1 = 12.12 ＋ 0.07 （Ge-R-CPBr） and lgK1 = 12.85 ＋ 0.06 （Ge-R-CTMaBr）. It is developed highly selective method of photometric determination of trace amounts of Ge（IV） in petroleum coke.
