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氧氟沙星—镁络合吸附波的研究 总被引:2,自引:0,他引:2
本文用多种电化学方法研究了氧氟沙星与镁离子的相互作用及其极谱伏安行为,在0.01mo1/L的NH3-NH4C1缓冲溶液中(pH=9.2),氧氟沙星与镁离子络合,产生一灵敏的还原峰,峰电位EP=-1.70V(vs.Ag/AgCl).该峰为不可逆的络合吸附峰,还原峰电流与镁离子浓度在4×10-6~2×10-5mol/L范围内呈良好的线性关系,可望用于镁离子的分析测定.本文还测定了该络合物的络合比,探讨了电极反应机理与络合物结构. 相似文献
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应用循环伏安法、微分脉冲伏安法对多菌灵在破碳电极上的电化学行为及其测定进行了研究。在pH=9.0的2mol/L NH3-NH4Cl底液中,对其进行循环伏安扫描,发现于0.61V(vs.Ag/AgCl)产生一灵敏的氧化峰。微分脉冲伏安法殉菌灵的检测限为4×10^-8mol/L。多菌灵的浓度在5.0×10^-7 ̄1.0×10^-5mol/L间与微分脉冲伏安峰电流呈线性关系(r=0.9942)。对于1× 相似文献
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头孢唑啉降解产物在银亚微盘电极上的电化学行为及其测定 总被引:3,自引:0,他引:3
基于头孢唑啉在 0.10mol/L NaOH溶液中水浴降解产物中含有巯基(-SH),在 pH 5.0NaAc-HAc介质中,于银亚微盘电极上产生一灵敏的吸附伏安氧化还原峰,其峰电位分别为 Epa=-0.530V和 EPc=-0.400V。动力学研究表明:电极反应的电子转移数为0.91,表观电子传递速率为ks=0.10s-1,峰电流与头孢唑啉浓度在1.0×10-6~50×10-1mol/L范围内呈良好的线性关系。方法可应用于人工合成样品头孢啉的检测。 相似文献
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一种基于形成杂多核络合物的荧光增敏效应的研究:Ⅲ.锰(Ⅱ),钴(… 总被引:3,自引:0,他引:3
本研究了Mn^2+和Co^2+对7-(8-羟基-3,6-二磺基萘偶氮)-8-羟基喹啉-5-磺酸-硼砂反应体系的混合荧光增敏作用。实验条件下,荧光增敏强度满足线性加和关系的范围是:Mn^2+浓度0 ̄2.9×10^-7mol/L;Co^2+浓度0 ̄8.8~10^-7mol/L;总浓度不超过1.0×10^-6mol/L。检出限量为Mn^2+4.5×10^-9mol/L和Co^2+1.4×10^-8mo 相似文献
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钒-槲皮素-氯酸盐体系极谱催化波的研究 总被引:1,自引:0,他引:1
在醋酸盐缓冲底液中,钒能与槲皮素形成络合物,并吸附在汞电极上,在氯酸盐存在下,在Ⅴ(Ⅳ)还原至Ⅴ(Ⅲ)过程中,形成催化波。用单扫二阶导数极谱法测定时,钒浓度在1.0×10 ̄(-9)~5.0×10 ̄(-6)mol/L与峰高有正比关系,检出下限为5.0×10 ̄(-10)mo1/mL。测得电活性络合物的组成为Ⅴ(Ⅳ:Qu=1:2。平行催化反应的速率常数K=1.5×10 ̄(4)(mol/L) ̄(-1)s(-1)。 相似文献
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本文报道一个光度法测定纳克量锡的新方法。在聚乙烯醇(PVA)存在下锡(Ⅳ)与钨酸盐和耐尔蓝(NB)反应形成离子缔合物,离子缔合物的最大吸收位于580nm,表观摩尔吸光系数ε值2.95×107L·mo1-1·cm-1,服从比耳定律范围0~2.0μg/L,检出限(3σ)0.083μg/L(n=10),对2.0μg/L锡测定的RSD为1.42%(n=11),离子缔合物至少稳定72h。考察了40多种共存离子的影响,大多数常见元素不干扰。测定锡的适宜条件[H2SO4]=1.20mo1/L,[WO2-4]=6.05×10-5mo1/L,[NB]=5.5×10-5mo1/L和PVA0.08%。本法已用于某些合金钢和锌合金中纳克量锡的测定,结果与推荐值吻合,回收率满意。 相似文献
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用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%. 相似文献
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Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction
Laurent Gavara Thomas Boisse Jean-Pierre Hénichart Adam Daïch Philippe Gautret 《Tetrahedron》2010,66(38):7544-5571
In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments. 相似文献
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The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula. 相似文献
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Rebecca J. Burton Mandy L. CrowtherNeal J. Fazakerley Shaun M. FilleryBarry M. Hayter Jason G. KettleCaroline A. McMillan Paula PerkinsPeter Robins Peter M. SmithEmma J. Williams Gail L. Wrigley 《Tetrahedron letters》2013
The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines. 相似文献
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KMnO4-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields. 相似文献
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N. A. Nedolya 《Chemistry of Heterocyclic Compounds》2008,44(10):1165-1219
The review contains a concise historical account and information on the most significant researches undertaken by the staff
at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry
of Heterocyclic Compounds.
Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008. 相似文献
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Regiospecific and direct imidation of the methyl C(sp3)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products. 相似文献
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《Tetrahedron》2014,70(21):3377-3384
The Rh(II)-catalyzed reaction of 2-carbonyl-substituted 2H-azirines with ethyl 2-cyano-2-diazoacetate or 2-diazo-3,3,3-trifluoropropionate provides an easy access to 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones. These compounds can be selectively prepared from the same starting material using temperature as the only varied parameter. The 2-azabuta-1,3-diene intermediate, a common precursor for both heterocyclic products, isomerizes into 2H-1,3-oxazine under kinetic control, while 1H-pyrrol-3(2H)-one is the sole product of the reaction at elevated temperatures. According to DFT-calculations a one-atom oxazine ring contraction involving ring-opening to a 2-azabuta-1,3-diene intermediate, followed by a 1,5- and 1,2-prototropic shift leads to the consecutive formation of imidoylketene and azomethine ylide, which then further undergo cyclization to the pyrrole derivative. 相似文献
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Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields. 相似文献