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11.
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Abstract

An efficient asymmetric oxidation of sulfides was achieved using (R)-6,6'-dibromo-BINOL as chiral ligand in combination with Ti(OiPr)4 using 70% aqueous tertiary butyl hydroperoxide as oxidant. The resulting sulfoxides had high enantiopurities and good yields. A range of aryl alkyl and aryl benzyl sulfides were oxidized to the corresponding sulfoxides with 78–95% ee in 72–80% yields.  相似文献   
13.
The novel octanuclear cluster [Mn8O2(OH)2(OMe)12(OAc)2(Mesalim)4] (1) presents SMM behaviour with a relatively high experimental energy barrier (eff/kB= 36.0 K) as shown by its dc and ac magnetic properties.  相似文献   
14.
Vanadate garnet systems namely Ca2NaMg2V3O12, individually doped with Dy and Sm and also co-doped with both the RE ions were synthesized via the solid-state reaction route and their photoluminescence (PL) properties were investigated. The method of synthesis was verified by the formation of single phase compound through X-ray diffraction (XRD) studies. Existence of energy transfer in between the host and the dopant ions was established by PL investigation. Color coordinates of all the compounds were calculated and plotted on the CIE diagram. It was seen that the co-doped system has a near white light emission. It was concluded that this single phosphor is capable of converting the ultraviolet emission of a UV-LED into white light.  相似文献   
15.
A novel protocol for intramolecular ketyl-olefin radical cyclization with low-valent titanium reagent is outlined. It allows the formation of the benzopyran nucleus from ortho-allyloxy propiophenones as the sole product in moderate yields via intramolecular radical cyclization.  相似文献   
16.
Americium from analytical solid waste containing U and metallic impurities was separated using hollow fiber supported liquid membrane (HFSLM) technique impregnated with DHOA–TODGA from nitric acid medium. An aliquot of 5 g of the solid waste containing Am (19.95 mg) as minor actinide and of U (2,588 mg), Fe (1,360 mg), Ca (1,810 mg) and Na (3,130 mg) as major impurities was processed. The feed solution obtained after the dissolution of the residue in ~4 M HNO3 was passed through HFSLM module. In the first stage using 1 M DHOA–dodecane U was recovered while Am and other impurities were left in the raffinate. In the second stage, 0.5 M DHOA + 0.1 M TODGA/dodecane was used for the separation of Am from other impurities. Though, majority of the elements were separated in this cycle, Ca was co extracted along with the americium. CMPO extraction chromatographic technique was used for further separation of americium from Ca. Significant decontamination factors were achieved in this three step separation process with respect to U, Fe, Na and Ca with ~77 % recovery of americium.  相似文献   
17.
Due to the multi-electronic nature, uranium is having line rich emission spectra and is expected to interfere during the determination of analytes at the trace level in uranium matrix. Therefore, chemical separation of uranium followed by the determination of trace metallic impurities in the raffinate by ICP-AES is generally adopted procedure in nuclear industries. There is restriction on choosing alternate analytical lines of elements by photomultiplier tube based ICP-AES associated with the polychromator while monochromator needs significant time to scan different analytical lines of all the elements. Since charged coupled detector (CCD) consists of array of pixels, it is having more option in choosing alternative analytical lines of the analytes. Therefore, an attempt was made to study the spectral interference of uranium on different analytical lines of analytes viz. Al, Ga, In, Si, Li, Ti, Mg, Sr, K, Ce, Nd, Lu, Sc, V, Er, Y, Ba, Bi, Pb, W, La, Tl, Sn, Yb, Mo, Sb, Pr and Zr; and the correction factors were evaluated (where ever necessary) using CCD based ICP-AES technique. The sensitivity and the detection limits of the analytical channels of the elements in presence of uranium matrix were calculated. The present study also deals with the identification of suitable analytical lines of uranium and its detection limits.  相似文献   
18.
We study the bremsstrahlung production of the ? meson in the reaction e+e? → e+e?? (→ e+e?π+π?). This reaction gives a C = ?1 background which complicates the study of C = +1 two-photon processes at the new colliding-beam facilities. The cross section for the reaction rises from approximately 0.3 nb to 0.7 nb as the beam energy increases from 2 GeV to 15 GeV. From a study of the distributions of the final leptons and pions, we find a suitable choice of cuts which will reduce the event rate down to a small fraction of R. It is not possible to attribute the three-prong events seen at DELCO and PLUTO to this particular production mechanism.  相似文献   
19.
20.
Lithium titanate ceramics doped with Eu were synthesized and their photoluminescence (PL) and emission spectral characteristics were investigated. PL spectra of the sample showed peaks corresponding to the 5D07FJ (J=0, 1, 2, 3 and 4) transitions under 230 nm excitation. The fluorescence lifetimes of Eu3+ ions were found out to be 645 μs. Strong red emission coming from the hypersensitive 5D07F2 transition of Eu3+ ion suggested the presence of the dopant ion in highly asymmetric environment. Further analysis of the emission spectrum revealed that the symmetry of the metal ion is very low i.e. C2. The emission intensity of the sample was compared with a commercial phosphor to get an idea about the commercial utility of the phosphor. Various emission properties for the system namely Judd-Ofelt intensity parameters, spontaneous emission probabilities, branching ratios, radiative lifetimes and quantum efficiency were evaluated for the dopant ion by adopting standard procedure.  相似文献   
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