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971.
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974.
Yali Fu Jingchang Zhang Zhong Huang Xiuyu Wang Yuguang Lv Weiliang Cao 《Journal of photochemistry and photobiology. A, Chemistry》2008,197(2-3):329-334
Four ternary complexes of Tb(III) were synthesized by introducing the first ligand (L1) (N-phenylanthranilic acid (N-HPA), α-furoic acid (FURA)) and the second ligand (L2) (1,10-phenanthroline (Phen), 2,2′-dipyridyl (Bipy)), respectively. These complexes were characterized by elemental analysis, infrared spectra, XRD, UV spectra and fluorescence spectra. The effect of L1 and L2 on the fluorescence properties of terbium complexes was discussed. It showed that all the complexes exhibited ligand-sensitized green emission. The fluorescent intensity increased in the sequence of Tb(FURA)3Bipy < Tb(N-PA)3Phen < Tb(FURA)3Phen < Tb(N-PA)3Bipy. It indicated that L1 affected fluorescence properties of the complexes differently when the corresponding L2 altered. Meanwhile, the influence of L2 on the luminescence properties of the complexes also depends on L1. The results showed that L1 and L2 affected each other and worked together as a whole. The matching of L1, L2 and Tb3+ ion is very important to the luminescence properties of Tb(III) ternary complexes. 相似文献
975.
1IntroductionAconsiderableresearcheforthasbeenmadeduringthepastfewyearstodevelopopticallogicoperationsbasedonphotorefractivem... 相似文献
976.
Ming Zhao Yuji Wang Caixia Huo Chunyu Li Xiaoyi Zhang Li Peng Shiqi Peng 《Tetrahedron: Asymmetry》2009,20(2):247-258
In lead detoxification, the α-anomer of N-glycocyl-l-amino acid is more potent than its β-anomer. Here a six-step-reaction route for stereoselectively preparing N-(α-l-arabinose-1-yl)-l-amino acids is reported. Treating l-arabinose with acetic anhydride and sodium acetate provided 1,2,3,5-tetra-O-acetyl-l-arabinofuranose in 90% yield. After removing the 1-acetyl group, the thus formed 2,3,5-tri-O-acetyl-l-arabinofuranose and N-(2-nitrophenylsulfonyl)-l-amino acid t-butylesters were treated with triphenylphosphine to perform Mitsunobu dehydration and form 2,3,5-tri-O-acetyl-l-arabinofuranosyl-l-[N-(2-nitrophenylsulfonyl)]amino acid t-butylesters 2a–f, and the ratios of their α- to β-anomer ranged from 8/1 to 9/1. Chromatographic separation provided epimerically pure 2a–f-α and 2a–f-β. In the presence of CF3CO2H, 2a–f-α and 2a–f-β were converted to α- and β-anomers of N-(2,3,5-tri-O-acetyl-l-arabinofuranosyl)-N-(2-nitrobenzenesulfonyl)-l-amino acids, 3a–f-α and 3a–f-β, in 87–92% yields. While in the presence of NaOCH3, 3a–f-α and 3a–f-β were converted to α- and β-anomers of N-(l-arabinofuranosyl)-N-(2-nitrobenzenesulfonyl)-l-amino acids, 4a–f-α and 4a–f-β, in 90–96% yields. Treating 4a–f-α and 4a–f-β with N-ethyldiisopropylamine (DIPEA) and thiophenol, their 2-nitrophenylsulfonyl groups were removed, and the α- and β-anomers of N-(l-arabinose-1-yl)-l-amino acids were formed in 70–79% yields. The bioassay confirmed that the lead detoxification activity of the α-anomer was significantly higher than that of the β-anomer. 相似文献
977.
Electron–hole recombination and photocorrosion are two challenges that seriously limit the application of two-dimensional (2D) transition metal dichalcogenides (TMDs) for photocatalytic water splitting. In this work, we propose a 2D van der Waals MoSe2/Ti2CO2 heterojunction that features promising resistance to both electron–hole recombination and photocorrosion existing in TMDs. By means of first-principles calculations, the MoSe2/Ti2CO2 heterojunction is demonstrated to be a direct Z-scheme photocatalyst for overall water splitting with MoSe2 and Ti2CO2 serving as photocatalysts for hydrogen and oxygen evolution reactions, respectively, which is beneficial to electron–hole separation. The ultrafast migration of photo-generated holes from MoSe2 to Ti2CO2 as well as the anti-photocorrosion ability of Ti2CO2 are responsible for photocatalytic stability. This heterojunction is experimentally reachable and exhibits a high solar-to-hydrogen efficiency of 12%. The strategy proposed here paves the way for developing 2D photocatalysts for water splitting with high performance and stability in experiments.The two challenges of electron–hole recombination and photocorrosion for two-dimensional transition metal dichalcogenides in the application of photocatalytic water splitting are simultaneously suppressed by rational design of heterojunctions. 相似文献
978.
The cyclic voltammetry, convolution voltammetry and chronopotentiometry were used to study the electrode process of Nd (III) reduced on iron electrode in molten NaCl-KCl-NdCl3 from 700 to 850°C. The electrodeposited products were analysed by X-ray diffraction. The results indicate that the intermetallic compound Fe2Nd forms first, and then the metallic neodymium deposits when Nd (III) is reduced on iron electrode. The Nd-Fe alloys rich in neodymium can be obtained by electrolysis with iron cathode in molten chlorides. The Nd-Fe alloys are composed of Fe2Nd and Nd. 相似文献
979.
By describing the evolution of a quantum state with the trajectories of the Majorana stars on a Bloch sphere,Majorana’s stellar representation provides an intuitive geometric perspective to comprehend the quantum system with highdimensional Hilbert space.However,the representation of a two-spin coupling system on a Bloch sphere has not been solved satisfactorily yet.Here,a practical method is presented to resolve the problem for the mixed-spin(s,1/2)system and describe the entanglement of the system.The system can be decomposed into two spins:spin-(s+1/2)and spin-(s?1/2)at the coupling bases,which can be regarded as independent spins.Besides,any pure state may be written as a superposition of two orthonormal states with one spin-(s+1/2)state and the other spin-(s?1/2)state.Thus,the whole initial state can be regarded as a state of a pseudo spin-1/2.In this way,the mixed spin decomposes into three spins.Therefore,the state can be represented by(2s+1)+(2s?1)+1=4s+1 sets of stars on a Bloch sphere.Finally,some examples are given to show symmetric patterns on the Bloch sphere and unveil the properties of the high-spin system by analyzing the trajectories of the Majorana stars on the Bloch sphere. 相似文献
980.
The calculation results of the R-branch transition emission spectra of(0–0) band of the A21 → X21 transition system of Sb Na molecule are presented in this paper. These R-branch high-lying transitional emission spectral lines are predicted by using the difference converging method(DCM). Our results show excellent agreement between DCM spectral lines and the experimental values, and the deviations are controlled within 0.0224 cm-1. What is more, based on the principle of over-determined linear equations, the prediction error is quantified in this work, which provides reliable theoretical support for our predicted DCM calculations. This work provides a lot of useful information for understanding the microstructure of Sb Na molecule. 相似文献