The title compound 2,5-bis(morpholino)-3,4-bis(p-chlorophenyl) thiophene 2 was obtained by the reaction of -thio-p-chlorobenzoyl thioformmorpholine 1 with trimethyl phosphite in refluxing xylene. The crystal is of tri...The title compound 2,5-bis(morpholino)-3,4-bis(p-chlorophenyl) thiophene 2 was obtained by the reaction of -thio-p-chlorobenzoyl thioformmorpholine 1 with trimethyl phosphite in refluxing xylene. The crystal is of triclinic, space group P?with unit cell constants: a = 6.0740(1), b = 10.3250(1), c = 19.779(2) , ?= 76.740(1), = 87.110(1), = 74.920(1), C24H24Cl2N2O2S, Mr = 475.41, Z = 2, V = 1165.7(3) ?, Dc = 1.354 g/cm3, (MoK) = 0.71073, = 0.392 mm-1, F(000) = 496, the final R = 0.0324 and wR = 0.0819 for 3102 observed reflections (I > 2(I)). X-ray analysis reveals that the two morpholinyl groups are located at the -position of thiophene, and the two p-chlorophenyl groups at the -position. Therefore, the title compound is a new symmetric thiophene derivative.展开更多
The title compound 2,5-dimorpholinyl-3,4-di(p-chlorophenyl)thiophene (C24H24Cl2N2O2S, Mr=475.41) was obtained by the reaction of a-(p-chlorothiobenzoyl)- thioformmorpholine with trimethyl phosphite. The crystal is tri...The title compound 2,5-dimorpholinyl-3,4-di(p-chlorophenyl)thiophene (C24H24Cl2N2O2S, Mr=475.41) was obtained by the reaction of a-(p-chlorothiobenzoyl)- thioformmorpholine with trimethyl phosphite. The crystal is triclinic, space group Pī, with unit cell constants a=6.074(1), b=10.325(1), c=19.779(2)? a=76.74(1), b=87.11(1), g=74.92(1), Z=2, V=1165.7(3)?, Dc=1.354g穋m-3, m (MoKa)=0.392mm-1, F(000)=496, R=0.0324, Rw=0.0458 for 3102 observed reflections(I>2s(I)). X-ray analysis reveals that interatomic distances for C(7)C(19) and C(8)C(20) are 1.368(2) and 1.365(2)? respectively, which shows that they are C=C double bonds. The atoms of C(7), C(8), C(19), C(20) and S form a thiophene ring and the morpholine adopts chair conformation.展开更多
[Na (N- (p-chlorophenyl ) aza-15--crown--5 ) (Et2O )]2 (Na2W0.5 Mo7.5 O26), Mr= 2119. 4, monoclinic, space group P21/c, a= 17. 803(4), b= 13. 674 (3), c= 14. 610(3), β= 112. 33(3)°, V=3290(1) A3, Z= 2, Dc= 2. 13...[Na (N- (p-chlorophenyl ) aza-15--crown--5 ) (Et2O )]2 (Na2W0.5 Mo7.5 O26), Mr= 2119. 4, monoclinic, space group P21/c, a= 17. 803(4), b= 13. 674 (3), c= 14. 610(3), β= 112. 33(3)°, V=3290(1) A3, Z= 2, Dc= 2. 139 g/cm3, μ= 1.704 mm-1, F (000) = 2079, R = 0. 026, Rw= 0. 030. The supermolecular complexconsists of one [Na2W0.5Mo7.5O28)2- anion in which only two Mo atoms are replaced byW in 25% (M= l/4W+3/4Mo) and the two Na+ are linked symmetrically to neighbouring [W0.5Mo7.5O26]4- units on the right and the left respectively and two complexcanons in which each Na+ deviates from the plane of the four ether oxygens and is coordinated to every hetero--atom in the crownether ring, and is also coordinated to the Oatom of Et2O.展开更多
The application of electron donor and electron shuttle substances has a vital influence on electron transfer,thus may affect the reductive dechlorination of 1,1,1-trichoro-2,2-bis（p-chlorophenyl）ethane（DDT） in ana...The application of electron donor and electron shuttle substances has a vital influence on electron transfer,thus may affect the reductive dechlorination of 1,1,1-trichoro-2,2-bis（p-chlorophenyl）ethane（DDT） in anaerobic reaction systems.To evaluate the roles of citric acid and anthraquinone-2,6-disulfonate（AQDS） in accelerating the reductive dechlorination of DDT in Hydragric Acrisols that contain abundant iron oxide,a batch anaerobic incubation experiment was conducted in a slurry system with four treatments of（1） control,（2） citric acid,（3） AQDS,and（4） citric acid ＋ AQDS.Results showed that DDT residues decreased by 78.93%-92.11% of the initial quantities after 20 days of incubation,and 1,1-dichloro-2,2-bis（4-chlorophenyl）-ethane（DDD） was the dominant metabolite.The application of citric acid accelerated DDT dechlorination slightly in the first 8 days,while the methanogenesis rate increased quickly,and then the acceleration effect improved after the 8th day while the methanogenesis rate decreased.The amendment by AQDS decreased the Eh value of the reaction system and accelerated microbial reduction of Fe（III） oxides to generate Fe（II）,which was an efficient electron donor,thus enhancing the reductive dechlorination rate of DDT.The addition of citric acid ＋ AQDS was most efficient in stimulating DDT dechlorination,but no significant interaction between citric acid and AQDS on DDT dechlorination was observed.The results will be of great significance for developing an efficient in situ remediation strategy for DDT-contaminated sites.展开更多
基金The project was supported by the Natural Science Foundation of Jiangsu Education Committee (99KJB 150001)
文摘The title compound 2,5-bis(morpholino)-3,4-bis(p-chlorophenyl) thiophene 2 was obtained by the reaction of -thio-p-chlorobenzoyl thioformmorpholine 1 with trimethyl phosphite in refluxing xylene. The crystal is of triclinic, space group P?with unit cell constants: a = 6.0740(1), b = 10.3250(1), c = 19.779(2) , ?= 76.740(1), = 87.110(1), = 74.920(1), C24H24Cl2N2O2S, Mr = 475.41, Z = 2, V = 1165.7(3) ?, Dc = 1.354 g/cm3, (MoK) = 0.71073, = 0.392 mm-1, F(000) = 496, the final R = 0.0324 and wR = 0.0819 for 3102 observed reflections (I > 2(I)). X-ray analysis reveals that the two morpholinyl groups are located at the -position of thiophene, and the two p-chlorophenyl groups at the -position. Therefore, the title compound is a new symmetric thiophene derivative.
文摘The title compound 2,5-dimorpholinyl-3,4-di(p-chlorophenyl)thiophene (C24H24Cl2N2O2S, Mr=475.41) was obtained by the reaction of a-(p-chlorothiobenzoyl)- thioformmorpholine with trimethyl phosphite. The crystal is triclinic, space group Pī, with unit cell constants a=6.074(1), b=10.325(1), c=19.779(2)? a=76.74(1), b=87.11(1), g=74.92(1), Z=2, V=1165.7(3)?, Dc=1.354g穋m-3, m (MoKa)=0.392mm-1, F(000)=496, R=0.0324, Rw=0.0458 for 3102 observed reflections(I>2s(I)). X-ray analysis reveals that interatomic distances for C(7)C(19) and C(8)C(20) are 1.368(2) and 1.365(2)? respectively, which shows that they are C=C double bonds. The atoms of C(7), C(8), C(19), C(20) and S form a thiophene ring and the morpholine adopts chair conformation.
文摘[Na (N- (p-chlorophenyl ) aza-15--crown--5 ) (Et2O )]2 (Na2W0.5 Mo7.5 O26), Mr= 2119. 4, monoclinic, space group P21/c, a= 17. 803(4), b= 13. 674 (3), c= 14. 610(3), β= 112. 33(3)°, V=3290(1) A3, Z= 2, Dc= 2. 139 g/cm3, μ= 1.704 mm-1, F (000) = 2079, R = 0. 026, Rw= 0. 030. The supermolecular complexconsists of one [Na2W0.5Mo7.5O28)2- anion in which only two Mo atoms are replaced byW in 25% (M= l/4W+3/4Mo) and the two Na+ are linked symmetrically to neighbouring [W0.5Mo7.5O26]4- units on the right and the left respectively and two complexcanons in which each Na+ deviates from the plane of the four ether oxygens and is coordinated to every hetero--atom in the crownether ring, and is also coordinated to the Oatom of Et2O.
基金supported by the National Natural Science Foundation of China (No.41201314)the Open Fund Project of State Key Laboratory of Soil and Sustainable Agriculture (No.0812201227)
文摘The application of electron donor and electron shuttle substances has a vital influence on electron transfer,thus may affect the reductive dechlorination of 1,1,1-trichoro-2,2-bis（p-chlorophenyl）ethane（DDT） in anaerobic reaction systems.To evaluate the roles of citric acid and anthraquinone-2,6-disulfonate（AQDS） in accelerating the reductive dechlorination of DDT in Hydragric Acrisols that contain abundant iron oxide,a batch anaerobic incubation experiment was conducted in a slurry system with four treatments of（1） control,（2） citric acid,（3） AQDS,and（4） citric acid ＋ AQDS.Results showed that DDT residues decreased by 78.93%-92.11% of the initial quantities after 20 days of incubation,and 1,1-dichloro-2,2-bis（4-chlorophenyl）-ethane（DDD） was the dominant metabolite.The application of citric acid accelerated DDT dechlorination slightly in the first 8 days,while the methanogenesis rate increased quickly,and then the acceleration effect improved after the 8th day while the methanogenesis rate decreased.The amendment by AQDS decreased the Eh value of the reaction system and accelerated microbial reduction of Fe（III） oxides to generate Fe（II）,which was an efficient electron donor,thus enhancing the reductive dechlorination rate of DDT.The addition of citric acid ＋ AQDS was most efficient in stimulating DDT dechlorination,but no significant interaction between citric acid and AQDS on DDT dechlorination was observed.The results will be of great significance for developing an efficient in situ remediation strategy for DDT-contaminated sites.
