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白细胞介素-2(IL-2)是机体免疫网络系统是起重要调节作用的淋巴因子,它能激活多种免疫细胞使其产生免疫活性。以^99 43Tc标记IL-2,用^9943Tc-二乙三胺五乙酸(DTPA)-IL-2的三元一系产物作为标记物进行检测,然后将标记物用于体内的IL-2受体显像的研究,有助于认识某些疾病的发生机理,可用于监测某些疾病的动态变化和实验性治疗。 相似文献
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Interleukin-2(IL-2)isa133-aminoacidlymphokineproteinsecretedbyactivatedT-cels.Itsbiologicalefectsaremediatedbybeingboundtospe... 相似文献
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提出间氨基酚(MAP)-H2O2-辣根过氧化物酶(HRP)伏安酶联免疫分析新体系并用于人血清中总甲状腺素(T4)的测定。本方法以线性扫描二阶导数伏安法检测HRP催化H2O2氧化MAP的产物,用于游离HRP和HRP标记物的测定,灵敏度均坑于经典的ELISA显色光度法。本法对总甲状腺素测定的线性范围为0.5-320mg/L。用所建立的方法对人血清样品进行了测定,并与现行的ELISA显色光度法对照,二者 相似文献
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过氧化氢氧化藏红T催化荧光法测定痕量铬(Ⅵ) 总被引:25,自引:4,他引:25
1引言在HAc-NaAc缓冲介质中,痕量铬(Ⅵ)对过氧化氢氧化藏红T的反应有强烈地催化作用,结果使藏红T的红色迅速减褪并伴随荧光减弱,建立了催化荧光法测定痕量铬(Ⅵ)的新方法。方法具有操作简便,灵敏度高,重现性好等特点,用于环境水样中铬(Ⅵ)的测定,结果满意。2实验部分2.1主要仪器与试剂日立M-850荧光分光光度计;930型荧光光度计;铬(Ⅵ)标准溶液:1 mg/L;藏红T溶液:4.0×10-4mol/L;30%H2O2溶液;pH4.2的HAc-NaAc缓冲溶液;水为二次去离子水。2.2实验方… 相似文献
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1,9-二(4-安替比林偶氮)嘌呤酮与钯的显色反应及其用于光度法测定钯 总被引:1,自引:0,他引:1
1引言 新合成的试剂1,9-二[4-安替比林偶氮]嘌呤酮(BAPD),在pH=4.50.的HAc-NaAc缓冲溶液中与Pd(Ⅱ)生成稳定的红色络合物,其λmax= 510 nm,把含量在0. 12~2.4 mg/L范围内与吸光度呈线性关系。据此建立了测定Pd(Ⅱ)的分析方法,并应用于电镀液和镀层中钯含量的测定。2实验部分2.1仪器与试剂 DU-7 HS型分光光度计(美国 Beckman公司);760 CRT型紫外-可见光分光光度计(上海第三分析仪器厂);HM-20E型酸度计(日本TOA公司)。钯标准溶液… 相似文献
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A new and high yielding method for the synthesis of [M(CO)(3)(eta(5)-2,3-C(2)B(9)H(11))](-) and the bifunctional metal complexes, rac-[M(CO)(3)(eta(5)-2-R-2,3-C(2)B(9)H(10))](-) (R = CH(2)CH(2)CO(2)H), from [M(CO)(3)Br(3)](2)(-) (M = Re, (99)Tc) was developed. The general approach entailed the addition of nido-[(C(2)B(9)H(12))(-)], or the acid substituted analogue, to [M(CO)(3)Br(3)](2)(-) (M = Re, (99)Tc) in the presence of TlOEt in THF. It was also possible to prepare the reported products in water using sodium carbonate in place of TlOEt. The reported approach led to the preparation, and X-ray crystallographic structure determination, of the first Tc-carborane complex reported to date (a = 13.606(17) A, b = 10.685(13) A, c = 15.534(16) A, alpha = gamma = 90 degrees, beta = 111.84(2) degrees). Because of the stabilities of the metal complexes, and the fact that the compounds can be prepared in water, the bifunctional derivatives can be considered as novel synthons for the preparation of organometallic (99m)Tc and (186/188)Re radiopharmaceuticals. 相似文献
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《Journal of Coordination Chemistry》2012,65(15):2356-2370
Technetium dimers Tc2(O2CCH3)4X2 (X =?Cl, Br) were synthesized and studied by X-ray Absorption Fine Structure spectroscopy (XAFS). EXAFS analysis gave for Tc2(O2CCH3)4Cl2: d Tc-Tc =?2.18(1) Å, d Tc–Cl =?2.43(1) Å and for Tc2(O2CCH3)4Br2: d Tc–Tc =?2.19(1) Å, d Tc-Br =?2.63(1) Å. The Tc Tc separations are in agreement with Raman studies while the Tc–X distances are somewhat larger. Comparison with other Tc(III) quadruply bonded dimers indicates that the carboxylate compounds exhibit larger Tc–Tc separations. The effect of the terminal ligand (nature and position) on the Tc–Tc separation is discussed. 相似文献
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[Tc(NBCl2Ph)Cl2(Me2PhP)3] and [Tc(NBH3)Cl2(Me2PhP)3] – the First Technetium Complexes with Nitrido Bridges between Technetium and Boron [TcNCl2(Me2PhP)3] reacts with BCl2Ph or BH3 · THF at low temperatures under formation of complexes containing a nitrido bridge between technetium and boron. The compounds are instable and decompose at room temperature under cleavage of the N–B bonds. The pale‐purple [Tc(NBCl2Ph)Cl2(Me2PhP)3] crystallizes in the orthorhombic space group Fdd2. The Tc≡N bond is only slightly lengthened by the formation of the N–B bond of 1.564(4) Å. However, a considerable lengthening of the Tc–Cl bond in trans position to the nitrido ligand is observed which can be attributed to an decreasing of the structural trans influence of the nitrido moiety. A similar structural feature can be found in [Tc(NBH3)Cl2(Me2PhP)3] which is the first structurally characterized transition metal complex containing a nitrido bridge to unsubstituted borane. 相似文献
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The distribution ratio of Mo(VI) and Tc(VII) in different acid media on D-2-EHPA-kieselguhr was studied in batch experiments. From these data a separation procedure for Mo-Tc is proposed, which consists in the selective elution of Tc(VII) and Mo(VI) by reverse-phase partition chromatography. The D-2-EHPA-kieselguhr column can also be used as a solid phase for a(99m)Tc generator. 相似文献
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The Raman and infrared spectra of gas phase Re(2)O(7) are reported. The experimental vibrational spectra of molecular Tc(2)O(7) and Re(2)O(7) are compared with calculated spectra. The results of these studies agree with a nonlinear M-O-M bridge for Tc(2)O(7) and Re(2)O(7). For infrared intensity calculations, the point charge approximation is used, while for the Raman calculations a combination of bond and atom polarizabilities is adopted. Pure Re(2)O(7) was prepared from rhenium wire, but attempts to prepare it from rhenium powder and oxygen always led to infrared spectra showing serious contamination from a species containing an -OH linkage. Detailed experiments identified this molecule as HReO(4), a unique transition metal analogue of the perhalic acids, and a partial infrared spectrum of this molecule is reported. 相似文献
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New ionic technetium complexes of the type trans-[Tc(PR3)4Cl2]+ are synthesized by various methods. The simplest method is the reaction of [TcO4]- with the phosphine in methanol in the presence of a chloride salt. Compounds containing PMe2Ph and PMe3 are synthesized and characterized by crystallographic methods. The complexes containing the less bulky phosphine can be prepared from complexes containing the bulker phosphine. The compounds are paramagnetic, with two unpaired electrons. The complexes studied by X-ray diffraction methods are the trans isomers. [Tc(PMe2Ph)4Cl2]PF6 crystallizes in the monoclinic space group P2(1)/c, with a = 11.511(2) A, b = 26.713(7) A, c = 12.688(3) A, beta = 92.79(1) degrees, Z = 4, and R1 = 0.0574. [Tc(PMe3)4Cl2]BPh4 (II) crystallizes in the orthorhombic space group Pbcn, with a = 18.213(5) A, b = 22.950(5) A, c = 19.428(6) A, Z = 8, and R1 = 0.0691. [Tc(PMe3)4Cl2]PF6 crystallizes in the monoclinic space group P2(1)/c, with a = 18.152(7) A, b = 16.838(9) A, c = 18.090(6) A, beta = 106.63(1) degrees, Z = 8, and R1 = 0.0670. The compounds all have octahedral coordination, but an important tetrahedral deformation of the plane containing the Tc and the four P atoms is observed in each case. In II, the two independent Tc atoms are both located on 2-fold axes. 相似文献
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Nitrosylation reactions are rare in the context of low valent Re(I)- and Tc(I)-tricarbonyl complexes so far. We herein describe a method for the conversion of a “M(CO)3-moiety” (M = Re, Tc) into a dicarbonyl-nitrosyl moiety “M(CO)2NO”, the synthesis of important precursor complexes and intermediates and possible applications for this new kind of Re- and Tc-chemistry.The behavior of the complex [ReCl3(CO)2(NO)]− in water was studied in detail and compared to that of [ReCl3(CO)3]2−. Contrary to the conversion of [ReCl3(CO)3]2− to the mixed aquo-carbonyl complex [Re(OH2)3(CO)3]+ in water, one chloride remains initially bound to the metal center in the dicarbonyl-nitrosyl complex, making [ReCl(OH2)2(CO)2(NO)]+ the main species for further reactions. In this context, we isolated and characterized the complex [Re(μ3-O)(CO)2(NO)]4. Examples of complexes with different bi- and tridentate ligands based on ReCl3(CO)2(NO)]− are discussed.For the development of potential new radiopharmaceuticals we also adapted the nitrosylation technique to the n.c.a. level with 99mTc. [99mTc(OH2)3(CO)3]+ served as starting material to form a 99mTc(CO)2(NO)-core. Labelling reactions with ligands such as iminodiacetic acid (IDA), nitrilotriacetic acid (NTA) and diethylenetriamine pentaacetic acid (DTPA) were performed, resulting in the complexes [99mTc(IDA)(CO)2(NO)], [99mTc(NTA)(CO)2(NO)] and [99mTc(DTPA)(CO)2(NO)]. In this way, the “nitrosyl-approach” adds a new and challenging synthetic tool to the already established organometallic chemistry of Re- and Tc-tricarbonyl complexes. 相似文献
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Dr. Ivana Radivojevic Jovanovic Dr. Colleen M. B. Gallagher Ramsey Salcedo Hossam Elshendidi Dr. Jacopo Samson Dr. Charles M. Drain Dr. Donna McGregor Dr. Wayne W. Lukens Jr. Dr. Benjamin P. Burton-Pye Dr. Lynn C. Francesconi 《欧洲无机化学杂志》2023,26(1):e202200507
Technetium-99 is a prevalent fission product from nuclear waste. The long half-life (211,000 yr) and environmental mobility of pertechnetate (TcO4−) render Tc particularly challenging to isolate and stabilize. Here we present two approaches for development of potential wasteforms using titanium dioxide, TiO2. Approach 1 is a low temperature chemical synthesis of TiO2 doped with Tc(IV) from TcO4− intended to mimic the Tc waste stream from the UREX family of separations and removes 98.5 % of the Tc, mainly present as edge-shared Tc(IV) pairs. Approach 2 utilizes TiO2 to photocatalytically reduce TcO4− to Tc(IV) stabilized on the surface of or within the TiO2 lattice. The %Tc removed from solution and adsorbed to TiO2 is pH dependent, with the maximum Tc(IV) adsorbed at pH 3–4 as either TcO2 or edge-sharing Tc(IV) octahedra. The Tc(IV)-TiO2 composites materials formed by both approaches are suitable for consolidation into a dense wasteform by Hot Isostatic Pressing (HIPing). 相似文献
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Grigoraviciute I Yamauchi H Karppinen M 《Journal of the American Chemical Society》2007,129(9):2593-2596
Among high-Tc superconductive copper oxides, there have been known phases that contain fluorite-structured layers as an additional "blocking block" between adjacent CuO2 planes. Here, we report that even a phase with the CuO2 planes separated by a 12-A thick quadruple-fluorite-layer block can be synthesized in a single phase and strongly oxygenated form to exhibit superconductivity with a Tc value as high as 55 K. The new phase is the fourth member of the (Cu,Mo)Sr2(Ce,Y)sCu2O(5+2s+delta) or (Cu,Mo)-12s2 homologous series. Comparison with the previously known s = 1, 2, and 3 members of the series reveals the amazing conclusion that Tc remains essentially unaffected upon inserting additional fluorite-structured layers between the two CuO2 planes as long as the hole-doping level of the planes is kept constant. 相似文献
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A new route to low-valent technetium complexes containing multiple acetonitrile ligands has been developed. The reduction of TcCl(4)(PPh(3))(2) with zinc metal dust in acetonitrile results in the formation of [Tc(CH(3)CN)(4)(PPh(3))(2)][Zn(2)Cl(6)](1/2). The hexafluorophosphate salt of the analogous Tc(II) cation can be prepared via chemical oxidation of the Tc(I) species, and the Tc(I) cation can be regenerated via chemical reduction. The compounds have been characterized in the solid state via single-crystal X-ray crystallography, and in solution via a combination of spectroscopic techniques and cyclic voltammetry. The structural parameters found in the two complexes are similar to each other; however, the difference in oxidation state is reflected, as expected, in the spectroscopic results. The electrochemical data, obtained from cyclic voltammograms of Tc(CH(3)CN)(4)(PPh(3))(2)](PF(6))(n)() (n = 1,2), mirror the synthetic results in that both compounds possess a reversible redox couple at -0.55 V versus ferrocene, which has been assigned to the Tc(II)/Tc(I) couple. 相似文献