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1.
研究了新试剂 1 -( 2 ,6 -二氯 -4 -硝基苯 ) -3 -( 4-硝基苯 ) -三氮烯与镉的显色反应。在 Triton X-1 0 0存在下 ,于 p H=9.8~ 1 1 .0的 Na2 B4 O7-Na OH缓冲溶液中 ,镉与试剂有高灵敏的显色反应 ,生成 1∶ 3型黄色配合物 ,最大吸收波长为 44 5nm。用双峰双波长法测定 ,其表观摩尔吸光系数为 2 .85× 1 0 5L·mol- 1·cm- 1。用拟定的方法测定了人发和废水中的镉含量 ,标准加入回收率分别为 1 0 4.5%和 1 0 5.8% ,相对标准偏差分别为 3 .2 %和 4.1 %。  相似文献   

2.
研究了新试剂1-(2,6-二氯-4-硝基苯)-3-(4-硝基苯)-三氮烯(DCNPNPT)与铜(Ⅱ)显色反应。在表面活性剂Tween-80存在下,pH 9.0~10.0范围内,铜(Ⅱ)与DCNPNPT形成1:4黄色配合物,其最大吸收波长为460nm,用双峰双波长法测定,表观摩尔吸光系数为1.I×10~5L·mol~(-1)·cm~(-1)。铜(Ⅱ)含量在0~240μg·L~(-1)范围内符合比耳定律。拟定方法用于铜矿和环境水标样中铜的测定,结果满意。  相似文献   

3.
报道了显色剂1-(4-硝基苯)-3-(3-甲基吡啶)-三氮烯的合成及其与锌的显色反应研究。在Triton X-100存在下,pH 11.0的硼砂-氢氧化钠缓冲溶液中,该试剂能与锌发生显色反应,锌与显色剂形成摩尔比为1∶4的黄色配合物,在445 nm波长处有最大正吸收峰,在535 nm波长处有最大负吸收。以445 nm为参比波长,535 nm为测量波长进行双波长测定,表观摩尔吸光系数为1.88×105L.mol-1.cm-1,锌浓度在0~12μg/25 mL范围内符合比耳定律。用拟定方法测定植物样品中微量锌,分析结果的相对标准偏差均小于2.5%,加标回收率在99.6%~100.4%之间。  相似文献   

4.
三氮烯试剂与第IB、IIB族金属元素有高灵敏的显色反应 1 [1] ,可用来测定样品中微量的Cd2 + 、Hg2 + 、Zn2 + 、Ni2 + 。随着表面活性剂引入该显色体系 ,使该试剂与金属离子显色反应的灵敏度有了很大的提高。目前报道的三氮烯显色剂与Hg2 + 显色反应的灵敏度一般在ε =1 .0× 1 0 5L·mol-1·cm-1左右 ,但也有部分试剂的灵敏度较高 ,如OC Cadion[2 ] 的ε =1 .77× 1 0 5L·mol-1·cm-1,DNAAB[3 ] ε=1 .74× 1 0 5L·mol-1·cm-1,MDAA[4]的ε=1 .8× 1 0 5L·mol-1·cm-1,APD…  相似文献   

5.
合成了新试剂(2,6-二氯-4-硝基苯)-3-(4-硝基苯)-三氮烯(DCNPNPT),测定了试剂的亚氨基离解常数pKa=9.2。在TritonX-100存在下,pH9.8~11.0范围内,试剂与Hg2+形成14黄色型配合物,用双波长法测得其表观摩尔吸光系数为2.27×105L·mol-1·cm-1。汞含量在0~10μg/25ml范围内符合比耳定律,用此法测定了天然水和实验室废水中微量汞含量,结果满意。  相似文献   

6.
研究了(2-苯并噻唑)-3-(4-硝基苯)-三氮烯(BTNPT)与Hg(Ⅱ)的反应,在非离子表面活性剂聚乙二醇辛基苯基醚(OP)及pH 10.1的缓冲溶液中,该试剂与汞可形成稳定的橙红色配合物,其表观摩尔吸光系数为4.9×105L·mol-1·cm-1,汞含量在4-1μg/25ml范围内符合比耳定律。  相似文献   

7.
研究了新显色剂1-(6-硝基-2-苯并噻唑)-3-(4-硝基苯)-三氮烯(NBTNPT)与锌的显色反应,在非离子表面活性剂TritonX-100存在下,pH10.1~10.8的Na2B4O7-NaOH缓冲溶液中,Zn2+与试剂能形成1∶2的橙黄色配合物,最大吸收波长为446nm,同时在528nm处配合物表现有最大负吸收,其表观摩尔吸光系数分别为ε=7.03×104L·mol-1·cm-1和ε=1.06×105L·mol-1·cm-1.用拟定的方法测定了人发和婴儿奶粉中的微量锌,结果令人满意.  相似文献   

8.
1-(2-羟基-5-硝基苯基)-重氮氨基偶氮苯与汞的显色反应   总被引:50,自引:0,他引:50  
环境监测中通常采用双硫腙法和冷原子吸收光度法测定有毒元素汞。也有用三氮烯试剂测定微量汞的报道。三氮烯试剂与第ⅠB、ⅡB族金属元素有高灵敏度的显色反应,可用来测定样品中微量的Cd2+、Hg2+、Zn2+、Cu2+等金属离子[1-3]。本文用新合成的显色剂1 (2 羟基 5 硝基苯基) 重氮氨基偶氮苯测定工业废水样品中的汞,结果满意。1 实验部分移取一定量的汞标准溶液(不大于12μg)于25ml容量瓶中,依次加入3 5ml的Na2B4O7 NaOH缓冲溶液(pH=10 5),1 5ml2%的TritonX 100溶液和2 5ml0 04%的HNPDAAB无水乙醇溶液,以水定容,摇匀,于25°C发色…  相似文献   

9.
合成了新的三氮烯试剂2 羟基4 磺酰氨基苯3 (4 硝基苯) 三氮烯(HSNPT) ,并研究了在TritonX 1 0 0表面活性剂存在下与镍的显色反应。在pH 1 0~1 2. 0的Na2 B4 O7 NaOH缓冲溶液中,试剂与镍形成配合比为3∶1型淡黄色配合物。配合物最大负吸收峰位于λ=5 40nm处,表观摩尔吸光系数1 .1 8×1 0 5L·mol- 1·cm- 1。Ni2 +的质量浓度在0~480 μg/L范围内符合比尔定律。用拟定方法测定合金钢样品中的微量镍,结果满意。  相似文献   

10.
新试剂1-(6-硝基-2-苯并噻唑)-3-(4-硝基苯)-三氮烯与汞(Ⅱ)显色反应的研究及应用金传明龚楚儒胡宗球杨明华(湖北师范学院化学系黄石435002)关键词1-(6-硝基-2-苯并噻唑)-3-(4-硝基苯)-三氮烯显色反应汞中图分类号O657....  相似文献   

11.
The photoprocesses of nifedipine, a 4-(2-nitrophenyl)-1,4-dihydropyridine, and nimodipine and nitrendipine, two 3-nitrophenyl Hantzsch-type analogues, were studied by steady-state and time-resolved methods. The intramolecular photoreduction of nifedipine into its nitrosophenyl product takes place within a few ns. The quantum yield of conversion is Φred = 0.3 and does not depend significantly on the oxygen concentration and solvent properties. Formation of the fully reduced 4-(2-aminophenyl)-1,4-dihydropyridine as minor product is indicated by fluorescence spectroscopy. The photoreduction of nimodipine and nitrendipine is inefficient, Φred = 0.002 in acetonitrile, but markedly enhanced in the presence of donors such as triethylamine (TEA) and 2-propanol, e.g. for TEA Φred is up to 0.03. The triplet states of nimodipine and nitrendipine were characterized. They react intermolecularly with TEA and 2-propanol, forming radicals as intermediates and eventually several reduction products.  相似文献   

12.
The preparation of 4-(3-nitrophenyl)-2-pieoline (3) was accomplished in one step by the Zecher-Krohnke ring-closure reaction. Compound 3 is the starling material for 2-lormyl-4-(3-arninophenyl)pyridine thiosemicarbazone (4-APPT), a promising antineoplastie agent.  相似文献   

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14.
Reaction of 3-nitrobenzaldehyde with diethyl oxalacetate in the presence of piperidine acetate and then ammonium acetate/acetic acid gave a moderate yield of tetraethyl 1,4-dihydro-4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarboxylate. This was oxidized with nitric acid to tetraethyl 4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarhoxylate which was hydrolyzed and decarboxylated to give 4-(3-nitrophenyl)pyridine.  相似文献   

15.
The spectral kinetic characteristics of the triplet states of 1-(4-nitrophenyl)-3-methylpyrazole (1) and 1-ethyl-3-(4-nitrophenyl)-5-chloropyrazole (2) were studied by the laser nanosecond photolysis technique in different solvents. The triplet lifetimes (τT) of molecules 1 and 2 were found to depend strongly on the solvent nature. An increase in τT by approximately two orders of magnitude on going from nonpolar and polar aprotic solvents (τT ≤ 15 ns) to aqueous-acetonitrile solutions (τT = 1100 ns for a volume acetonitrile to water ratio of 1 : 3) was analyzed, taking into account the influence of the medium on the relative contribution of the n,π*- and π,π*-configurations to the lowest triplet state. __________ Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1115–1119, May, 2005.  相似文献   

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