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We reported on a new amperometric sensor for the sensitive and selective determination of iodate in table salt. The iodate sensor was constructed by the integration of a novel nanocomposite which was made from 9,10-phenanthrenequinone(PQ) and graphene(GP) with a glassy carbon electrode(GCE). The synthesized graphene and the nanocomposite were well characterized by X-ray diffraction(XRD), transmission electron microscopy(TEM), Fourier transform infrared(FTIR) spectroscopy and Raman spectroscopy. We fully studied the electrochemical behavior and kinetic characteristics of the PQ/GP nanocomposite at GCE. The PQ/GP electrode shows a good electrochemical catalytic activity towards the reduction of iodate, which makes itself a sensitive and selective electrochemical sensor for iodate. The iodate sensor displays a high sensitivity(1.04 mA·mmol·L-1), a low detection limit(1.0×10-8 mol/L), a rapid response(less than 2 s), and a broad linear range(from 5.0×10-8 mol/L to 6.0×10-3 mol/L ). In addition, the sensor is interference free. The practical application of the proposed sensor was tested by the detection of iodate in table salt. 相似文献
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用循环伏安法研究了2-氨基-9,10-蒽醌及其衍生物在DMF-0.1mol/LTBAP溶液中的电化学行为,结果表明它们在铂电极上均发生两步连续的单电子还原过程,取代基R及水和苯甲酸等质子性试剂的加对伏安曲线有很大的影响。 相似文献
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N. A. Len’shina M. Yu. Zakharina R. S. Kovylin M. A. Baten’kin T. I. Kulikova M. V. Arsen’ev S. A. Chesnokov 《High Energy Chemistry》2018,52(5):378-383
The effective rate constants for the photoreduction (kH) of 9,10-phenanthrenequinone (PQ) in the presence of dimethacrylate monomers (ethylene glycol dimethacrylate (DMEG), triethylene glycol dimethacrylate (TGM-3), and oligocarbonate dimethacrylate (OKM-2)) and porous polymers based on them have been spectrophotometrically determined. The values of kH in the presence of DMEG and TGM-3 in benzene solutions and in the monomer media are two times greater than in the presence of OKM-2. The values of kH for PQ in pores of polyDMEG, polyTGM-3, and polyOKM-2 are approximately identical and do not depend on the pore size (up to hundreds of nanometers) and the specific surface area. 相似文献
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Photoreduction of 9,10-phenanthrenequinone (PQ) in the presence of p-substituted N,N-dimethylanilines and polymethylbenzenes affords corresponding phenolethers as primary products. In the subsequent process shielded from light, phenolethers, which were formed by photoreaction of PQ with N,N-dimethylanilines, were quantitatively converted to give corresponding ketols. Phenolethers of 9,10-phenanthrenequinone and polymethylbenzenes are rearranged only under irradiation and in the presence of second molecule of PQ to form ketols. Stability of phenolethers is determined by redox properties and structure of hydrogen donors. 相似文献
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The basic characteristics of anthracene(AN) and dibenz[a,c]anthracene(D[a,c]A) derivatives, important semiconductors, were systematically studied. Differential scanning calorimetry(DSC) shows that D[a,c]A has the reversibility of solid and liquid phases. Thermalgravimetric analysis(TGA) shows that D[a,c]A exhibits higher Td(decomposition temperature), which indicates D[a,c]A, as active layers, should be more suitable to being made into stable devices. D[a,c]A shows blue-shifted UV-Vis absorption and emission despite increased conjugation compared to anthracene due to different symmetries. Both the compounds are planar and show weak blue fluorescence in the tetrahydrofuran(THF) solution and higher fluorescence in the solid-state, due to different energy levels in solution and solid-state, explained via Jablonski diagram. 相似文献
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Current attempts to bridge the fields of what is conventionally called ‘electrocatalysis’ and of molecular catalysis of electrochemical reactions are surveyed and discussed. It amounts in many cases to ‘heterogenize’ molecular catalytic systems. Information on the meso- to nanostructures of the resulting catalytic films forms the basis of the understanding of new modes of transport of the reactants (catalysts, substrates and cosubstrates, products) that may govern the mechanistic competitions and consequently selectivity. Efforts to adapt benchmarking procedures developed in homogeneous molecular catalysis (catalytic Tafel plots) should be encouraged, taking into account, as additional factors, the transport of electrons and reacting species (including gases) through the catalytic system. 相似文献
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1,8-二羟基-9,10-二氢蒽的合成 总被引:1,自引:0,他引:1
以1,8-二羟基蒽醌为原料,经甲醚化,锌粉和金属钠还原,去甲基等4步反应合成1,8-二羟基-9,10-二氢蒽,总产率为37.1,8-二甲氧基蒽醌用NaBH4/CF3COOH还原生成二聚产物,并测定了其单晶结构. 相似文献
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合成了反式-9,10-二氢-9,10-二乙基蒽-11,12-二羧酸(EADA)及其与硼酸共同构建主体晶格的正四丁基铵阳离子管状包合物(n-C4H9)4N C18H13O-4?B(OH)3(1)和(n-C4H9)4N C18H13O-4(2),并通过单晶X射线衍射法对其进行了晶体结构测定.结果表明,晶体1属单斜晶系,P2(1)/c空间群,晶胞参数a=1.5699(1)nm,b=0.9955(6)nm,c=2.2933(1)nm,β=109.962(3)°,Z=4,R1=0.0434,wR=0.0759;晶体2属单斜晶系,C2/c空间群,晶胞参数a=1.4005(3)nm,b=1.2821(2)nm,c=1.7657(3)nm,β=100.388(1)°,Z=4,R1=0.0584,wR=0.0966.在晶体1中,EADA阴离子和硼酸分子的氢键四聚体链交错平行排列,生成具有矩形截面的管道式主体晶格,每个管道内包含了两列规则排列的正四丁基铵阳离子(n-C4H9)4N .在晶体2中,相互独立的EADA阴离子交错排列形成类蜂巢形截面的管道式主体晶格,正四丁基铵阳离子形成Z形长列被包合在这些管道里,阳离子的烃链穿插在管道壁中. 相似文献
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李宗良 《化学物理学报(中文版)》2011,24(2):194-198
Based on the first-principles computational method and the elastic scattering Green's func-tion theory, we have investigated the electronic transport properties of different oligothio-phene molecular junctions theoretically. The numerical results show that the difference of geometric symmetries of the oligothiophene molecules leads to the difference of the contact configurations between the molecule and the electrodes, which results in the difference of the coupling parameters between the molecules and electrodes as well as the delocalization properties of the molecular orbitals. Hence, the series of oligothiophene molecular junctions display unusual conductive properties on the length dependence. 相似文献
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Kazakov G. G. Druzhkov N. O. Cherkasov V. K. 《Russian Journal of Coordination Chemistry》2020,46(3):178-192
Russian Journal of Coordination Chemistry - The synthesis of N-hetero analogs of 9,10-phenanthrenequinones is discussed. The features of their structure are considered. Information on the use of... 相似文献
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阻燃抗氧剂9,10-二氢-9-氧杂-10-膦菲-10-氧的合成 总被引:2,自引:0,他引:2
Phenylphenol,phosphorus trichloride and aluminium trichloride were mixed and rea cted between 60~215℃ for about 11h,then vacuum-distill ed at 202~235℃ under pressure of -750mmHg.The distillate was added to sodium c arbonate solution for hydrolysis.The product was then crystallized by acid,filte red,dried.Vacuum-dehydration reaction and grinding were followed to give the ti tle product. 相似文献
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Bromodimethylsulfonium bromide(BDMS) was used as an efficient brominating reagent for the synthesis of 9,10-dibromoanthracene in dichloromethane. The desired products were obtained in excellent yields. 相似文献
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HTPB与Al不同晶面结合能和力学性能的分子动力学模拟 总被引:3,自引:0,他引:3
采用分子力学(MM)和分子动力学(MD)方法, 在250、300、350、400、450 K, 对固体推进剂端羟基聚丁二烯(HTPB)和铝晶胞不同晶面结构所组成的层模型在COMPASS力场下, 进行模拟计算, 求得结合能和静态力学性能(弹性系数、模量和泊松比). 模拟结果表明, 在400 K时HTPB与Al(011)面的结合能最大, 从综合力学性能优劣上看, 各个面从优到劣的排序为(011)>(221)>(001), HTPB与Al的结合能与力学性能具有对应关系, 结合能大的力学性能优异, 结合能小的力学性能较差. 相似文献