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71.
72.
Tian-Qun Yu Yong-Sheng Hou Yi Jiang Wen-Xuan Xu Tao Shi Xia Wu Jin-Chao Zhang Dian He Zhen Wang 《Tetrahedron letters》2017,58(22):2084-2087
N-Substituted benzo[d]isothiazol-3(2H)-ones are a family of compounds with extremely important application. Recently, we have developed a new green pathway to synthesize these compounds via potassium bromide-catalyzed intramolecular oxidative dehydrogenative cyclization. This reaction has high functional group tolerance and affords excellent yield even in gram scale. 相似文献
73.
LIN Bi-Zhou HAN Guo-Hua DING Cong LIU Xue-Zhong BAI Ling 《结构化学》2007,26(9):1107-1111
A hybrid organic-inorganic material (H2enMe)[Mo3O10] (C3H12Mo3N2O10, Mr = 523.97) has been synthesized under hydrothermal conditions and its crystal structure was determined by X-ray diffraction. It crystallizes in the orthorhombic system, space group Pnma with a = 12.430(2), b = 7.6089(12), c = 11.9553(19) , V = 1130.7(3) 3, Dc = 3.078 g/cm3, Z = 4, μ(MoKa) = 3.328 mm1, F(000) = 1000, the final R = 0.0256 and wR = 0.0716 for 1314 observed reflections with I > 2σ(I). A total of 11780 reflections were measured and 1325 were unique (Rint = 0.0244). It consists of infinite one-dimensional edge-sharing MoO6 octahedral chains with [Mo3O10]2 moieties. The protonated diaminopropane cations are located between the chains and linked to the oxygen atoms of the inorganic skeletal backbones by hydrogen bonds. It is indicated that the as-synthesized compound displays photochromic property in the solid state. 相似文献
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本文报导了傅里哀变换红外发射光谱法研究多相氧化物催化剂的实验装置的建立及实验条件的考察。设计加工了一个温度范围宽,可在各种气氛和真空条件下原位研究氧化物催化剂的红外发射池。以MoO_3为例,考察了样品厚度,测试温度对发射光谱的影响。当样品量小于1mm·cm~(-2)时,随样品量增加,谱峰强度线性增加,但峰形不发生变化。当样品量高于1mg.cm~(-2)时,随样品量增加,谱图严重畸变。随样品温度升高,谱峰强度近似线性增加。并用该方法研究了MoO_3在还原和再氧化过程中表面氧物种的变化。结果表明桥式MO?O?Mo物种比端基Mo=O物种较易还原,再氧化时,Mo=O物种比Mo?O?Mo物种优先形成。 相似文献
76.
Addition of hydrochloric or hydrobromic acid to a solution of potassium permanganate in acetonitrile produced a homogeneous mixture, which is suitable for laboratory chlorination or bromination, respectively. Aromatic compounds more reactive than alkylbenzenes can be chlorinated or brominated without additional catalyst. Alkenes and alkynes give the corresponding vicinal dihaloalkanes and vinyl halides. All reactions complete within two hours under mild condition (25-60 °C) with excellent to moderate yields. 相似文献
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78.
碘化钾-乙基紫-水体系固相浮选分离镉的研究 总被引:4,自引:0,他引:4
研究了碘化钾 乙基紫 水体系固相浮选分离镉的行为及与常见金属离子分离的最佳条件。试验表明,将碘化钾溶液、乙基紫溶液和盐酸溶液混合稀释,生成稳定的CdI2-4·(EV+)2三元缔合物可很快浮于水相,使Cd(Ⅱ)被定量浮选。控制适当条件,可实现Cd(Ⅱ)与常见金属离子Mn(Ⅱ)、Al(Ⅲ)、Ni(Ⅱ)、Zn(Ⅱ)之间的分离。对合成水样进行了浮选分离测定,结果满意。 相似文献
79.
Metal nanoparticles are nanosized structures that have different potential applications in biological, chemical, medical, and agricultural fields because of their exotic characteristics. Their size ranges from 1 to 100 nm. Metal nanoparticles are either purer forms of metals (eg: Gold, Silver, Copper, Iron, etc.) or their compounds (eg: sulfides, hydroxides, oxides, etc.). Ionic liquids are generally used in the extraction of nanoparticles but they are challenging because of their indigent bio-degradability, bio-compatibility, and sustainability. So Deep Eutectic Solvent (DES) is reported as an alternative to ionic liquids in the formation of nanoparticles. The DESs are a complex of quaternary ammonium salts and hydrogen donors or metal salt. DESs contain higher non-symmetric ions which have lower lattice energy and hence they have a lower melting point. This research utilizes a novel DES (choline chloride – urea) as an effective solvent to produce mercuric sulfide (HgS), zirconium oxide (ZrO), manganese oxide (MnO), and copper oxide (CuO) nanoparticles. As a result, the production of these metal nanoparticles using Choline Chloride (C5H14ClNO) – Urea DES can be treated as a promising way in chemical manufacturing. The nanoparticles have been analyzed using Ultra Violet Spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FT-IR), X-Ray Diffraction (XRD) and Energy Dispersive X-Ray Analysis (EDAX). 相似文献
80.
K.B. Ibrahim W.-N. Su M.-C. Tsai A.W. Kahsay S.A. Chala M.K. Birhanu J.-F. Lee B.J. Hwang 《Materials Today Chemistry》2022
Developing oxygen evolution reaction (OER) electrocatalyst based on earth-abundant materials holds great promise for ascertaining water-splitting to surmount its deprived kinetics. In this regard, NiFe-LDH (layered double hydroxide) receives considerable attention owing to their layered structure. However, they still suffer from poor electronic conductivity and structural stability. We combined NiFe-LDH nanosheets with Magnéli phase Ti4O7 into a heterostructured composite. A series of analyses reveal that decorating Ti4O7 facilitates charge transfer to enhance the conductivity of NiFe-LDH-Ti4O7. During electrochemical measurement, Ni2+ is transformed to metastable Ni3+ (Ni (OH)→ NiOOH) before the OER onset potential. Thus, the presence of Ni3+ as the main active sites could improve the chemisorption of OH? to facilitate OER. As a result, the NiFe-LDH-Ti4O7 catalyst delivers as low as onset potential (1.43 V). Combining the holey structure (NiFe-LDH and Ti4O7) and the defect engineering generated on NiFe-LDH-Ti4O7 as a synergistic effect improves the OER performance. The inclusion of Ti4O7 in the composite leads to more vacancy sites, as evidenced by the extended X-ray absorption fine structure (EXAFS) analysis. The obtained defective structure with a low coordination environment would improve the electronic conductivity and facilitate the adsorption process of H2O onto metal cations, thereby increasing the intrinsic catalytic activity of NiOOH. The strong coupling of NiFe-LDH and Ti4O7 also increases the stability, and the heterostructured composite helps maintain the structural robustness of the LDH. 相似文献