建立了一种土壤中2,4-D的液相色谱-串联质谱的检测分析方法。样品经酸化乙腈提取,浓缩定容后过0.22μm微孔滤膜,采用色谱柱分离,以乙腈和0.25%甲酸溶液为流动相进行梯度洗脱,采用电喷雾ESI离子源方式和多信号扫描,外标法定量。在10.0~1...建立了一种土壤中2,4-D的液相色谱-串联质谱的检测分析方法。样品经酸化乙腈提取,浓缩定容后过0.22μm微孔滤膜,采用色谱柱分离,以乙腈和0.25%甲酸溶液为流动相进行梯度洗脱,采用电喷雾ESI离子源方式和多信号扫描,外标法定量。在10.0~1000μg/kg的质量浓度范围内,相关系数R^(2)为0.9999,该方法的定量检测限为10.0μg/kg。进行100μg/kg、200μg/kg和1000μg/kg三个不同水平浓度的添加回收试验,2,4-D的回收率在75.91%~98.05%之间,RSD介于5.94%~18.75%之间。该方法操作简单、灵敏度高、快速准确。利用该方法测定土壤中2,4-D残留量,施药后2 h 2,4-D在土壤上的原始附着量为73.4μg/kg,第21天残留量为≤10.0μg/kg,消解率为≥86.38%,半衰期T1/2为5.42 d。展开更多
The title compound （E）-4-tert-butyl-N-（2,4-dichlorobenzylidene）-5-（1,2,4-triazol-1-yl）-thiazol-2-amine was synthesized by the reaction of 4-tert-butyl-5-（1,2,4-triazol-1-yl）-thiazol-2-amine with 2,4-dichlorobe...The title compound （E）-4-tert-butyl-N-（2,4-dichlorobenzylidene）-5-（1,2,4-triazol-1-yl）-thiazol-2-amine was synthesized by the reaction of 4-tert-butyl-5-（1,2,4-triazol-1-yl）-thiazol-2-amine with 2,4-dichlorobenzaldehyde, and its crystal structure was determined by singlecrystal X-ray diffraction. The crystal belongs to the triclinic system, space group P1 with a = 7.9748（4）, b = 10.1803（5）, c = 11.4603（6）, α = 102.882（1）, β = 100.253（1）, γ = 104.457（1）°, V = 850.95（7）3, Z = 2, F（000） = 392, C16H15Cl2N5S, Mr = 380.29, Dc = 1.484 g/cm3, S = 1.095, μ = 0.512 mm-1, the final R = 0.0301 and wR = 0.0965 for 3334 observed reflections （I 〉 2σ（I））. The preliminary antitumor activity shows that for the title compound the IC50 of Hela is 0.175 μmol/mL and that of Bel7402 is 0.156 μmol/mL.展开更多
The title compound N-tert-butyl-N(-(2,4-dichlorobenzoyl)-N-[1-(4-chlorophenyl)- 1,4-dihydro-6-methylpyridazine-4-oxo-3-carbonyl]hydrazine [(C23H_21N4O3Cl3)2·1.5H_2O, Mr = 1042.60] was prepared by the reaction of ...The title compound N-tert-butyl-N(-(2,4-dichlorobenzoyl)-N-[1-(4-chlorophenyl)- 1,4-dihydro-6-methylpyridazine-4-oxo-3-carbonyl]hydrazine [(C23H_21N4O3Cl3)2·1.5H_2O, Mr = 1042.60] was prepared by the reaction of 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6- methylpyridazine-3-carboxylic acid with chloroformate ethyl ester, then with N′-tert-butyl-N- (2,4-dichlorobenzoyl) hydrazine in the present of triethylamine. The crystal structure has been determined by X-ray diffraction. The crystal belongs to Monoclinic, space group P21/c, with unit cell constants a =11.4948(9), b=12.7495(10), c=35.854(3) ?, β =92.964(2)°, Z=4, V=5247.6(7) ?3, Dc = 1.320 Mg/m3, F(000) = 2156 , μ (MoKa)= 0.385, R = 0.0661, wR = 0.1875, for 9151 observed reflections( I >2σ(I)). The structure is a dimer linked by intermolecular hydrogen bond which can be observed between N(1)- H...O(6), N(5)- H...O(3). The distances are 2.068 and 2.027? respectively.展开更多
文摘建立了一种土壤中2,4-D的液相色谱-串联质谱的检测分析方法。样品经酸化乙腈提取,浓缩定容后过0.22μm微孔滤膜,采用色谱柱分离,以乙腈和0.25%甲酸溶液为流动相进行梯度洗脱,采用电喷雾ESI离子源方式和多信号扫描,外标法定量。在10.0~1000μg/kg的质量浓度范围内,相关系数R^(2)为0.9999,该方法的定量检测限为10.0μg/kg。进行100μg/kg、200μg/kg和1000μg/kg三个不同水平浓度的添加回收试验,2,4-D的回收率在75.91%~98.05%之间,RSD介于5.94%~18.75%之间。该方法操作简单、灵敏度高、快速准确。利用该方法测定土壤中2,4-D残留量,施药后2 h 2,4-D在土壤上的原始附着量为73.4μg/kg,第21天残留量为≤10.0μg/kg,消解率为≥86.38%,半衰期T1/2为5.42 d。
基金Supported by the Natural Science Foundation of Hunan Province (No. 07JJ302)
文摘The title compound （E）-4-tert-butyl-N-（2,4-dichlorobenzylidene）-5-（1,2,4-triazol-1-yl）-thiazol-2-amine was synthesized by the reaction of 4-tert-butyl-5-（1,2,4-triazol-1-yl）-thiazol-2-amine with 2,4-dichlorobenzaldehyde, and its crystal structure was determined by singlecrystal X-ray diffraction. The crystal belongs to the triclinic system, space group P1 with a = 7.9748（4）, b = 10.1803（5）, c = 11.4603（6）, α = 102.882（1）, β = 100.253（1）, γ = 104.457（1）°, V = 850.95（7）3, Z = 2, F（000） = 392, C16H15Cl2N5S, Mr = 380.29, Dc = 1.484 g/cm3, S = 1.095, μ = 0.512 mm-1, the final R = 0.0301 and wR = 0.0965 for 3334 observed reflections （I 〉 2σ（I））. The preliminary antitumor activity shows that for the title compound the IC50 of Hela is 0.175 μmol/mL and that of Bel7402 is 0.156 μmol/mL.
文摘The title compound N-tert-butyl-N(-(2,4-dichlorobenzoyl)-N-[1-(4-chlorophenyl)- 1,4-dihydro-6-methylpyridazine-4-oxo-3-carbonyl]hydrazine [(C23H_21N4O3Cl3)2·1.5H_2O, Mr = 1042.60] was prepared by the reaction of 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6- methylpyridazine-3-carboxylic acid with chloroformate ethyl ester, then with N′-tert-butyl-N- (2,4-dichlorobenzoyl) hydrazine in the present of triethylamine. The crystal structure has been determined by X-ray diffraction. The crystal belongs to Monoclinic, space group P21/c, with unit cell constants a =11.4948(9), b=12.7495(10), c=35.854(3) ?, β =92.964(2)°, Z=4, V=5247.6(7) ?3, Dc = 1.320 Mg/m3, F(000) = 2156 , μ (MoKa)= 0.385, R = 0.0661, wR = 0.1875, for 9151 observed reflections( I >2σ(I)). The structure is a dimer linked by intermolecular hydrogen bond which can be observed between N(1)- H...O(6), N(5)- H...O(3). The distances are 2.068 and 2.027? respectively.
