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1.
The stereoselective intramolecular cyclizations of bis(cinnamyl)tosylamides and dimethyl bis(cinnamyl)malonates mediated by cerium(IV) ammonium nitrate leading to the synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes are described.  相似文献   
2.
A bishydrazone was prepared by reacting isatin monohydrazone with 2-hydroxy-1-naphthaldehyde and a series of metal complexes with this new ligand were synthesised by reaction with MnII, FeII, CoII, NiII, CuII and ZnII salts. The complexes were characterised on the basis of elemental analysis, molar conductance, magnetic susceptibility data, u.v.–visible, i.r., e.s.r. and n.m.r. spectral studies, wherever possible and applicable. Analytical data reveal that the nickel(II), copper(II) and zinc(II) complexes possess 1:1 metal–ligand ratios and that manganese(II), iron(II) and cobalt (II) complexes exhibit 1:2 ratios. Infrared spectral data suggest that the bishydrazone behaves as a monobasic tridentate ligand with ONO donor sequence towards the metal ions. X-ray diffraction study of the copper(II) complex indicated an orthorhombic crystal lattice. The e.p.r. spectral data show that the metal–ligand bond has considerable covalent character. The electrochemical behaviour of the copper(II) complex was investigated by cyclic voltammetry (CV). Antibacterial tests of the ligand and the metal complexes were also carried out and it has been observed that the complexes are more potent bactericides than the ligand.  相似文献   
3.
A facile CAN-mediated oxidative rearrangement of alkoxyaryl cyclobutanes and oxetanes is described.  相似文献   
4.
The effect of impurities on the growth of manganese carbonate crystals has been studied. Stereophotogrammetric analysis showed that all crystal faces have the same Miller indices and the peanut-shaped forms are twins with twin axis 0001.  相似文献   
5.
Cerium oxide‐filled high density polyethylene (HDPE) composites for microwave substrate applications were prepared by sigma‐blend technique. The HDPE was used as the matrix and the dispersion of CeO2 in the composite was varied up to 0.5 by volume fraction, and the dielectric properties were studied at 1 MHz and microwave frequencies. The variations of thermal conductivity (keff), coefficient of thermal expansion (αc) and Vicker's microhardness with the volume fraction of the filler were also measured. The relative permittivity (εeff) and dielectric loss (tan δ) were found to increase with increase in CeO2 content. For 0.4 volume fraction loading of the ceramic, the composite had εeff = 5.7, tan δ = 0.0068 (at 7 GHz), keff = 2.6 W/m °C, αc = 98.5 ppm/°C, Vicker's microhardness of 18 kg/mm2 and tensile strength of 14.6 MPa. Different theoretical approaches have been used to predict the effective permittivity, thermal conductivity, and coefficient of thermal expansion of composite systems and the results were compared with the experimental data. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 998–1008, 2010  相似文献   
6.
The MgAl2O4 ceramics were prepared by the conventional solid-state ceramic route and the dielectric properties studied in the microwave frequency region (3–13 GHz). The phase purity and crystal structure were identified using the X-ray diffraction technique. The MgAl2O4 spinel ceramics show interesting microwave dielectric properties (εr=8.75, Quxf=68900 GHz (loss tangent = 0.00017 at 12.3 GHz), τf=-75 ppm/°C). The MgAl2O4 has high negative τf, which precludes its immediate use in practical applications. Hence the microwave dielectric properties of MgAl2O4 spinels were tailored by adding different mole fractions of TiO2. The εr and Q factor of the mixed phases were increased with the molar addition of TiO2 into the spinel to form mixtures based on (1-x)MgAl2O4-xTiO2 (x=0.0-1.0). For x=0.25 in (1-x)MgAl2O4-xTiO2, the microwave quality factor reaches a maximum value of Quxf=105400 GHz (loss tangent = 0.00007 at 7.5 GHz) where εr and τf are 11.035 and -12 ppm/°C, respectively. The microwave dielectric properties of the newly developed 0.75MgAl2O4-0.25TiO2 dielectric is superior to several commercially available low loss dielectric substrates. PACS 77.22.-d; 84.40.-x; 81.05.Je  相似文献   
7.
Nair V  Biju AT  Mohanan K  Suresh E 《Organic letters》2006,8(11):2213-2216
[reaction: see text] Reaction of the Huisgen zwitterion, derived from triphenylphosphine and dialkyl azodicarboxylate, with allenic esters affords highly functionalized pyrazolines and pyrazoles. The crystal structure of pyrazoline derivative 7a showed extensive C-H...O interactions. Pyrazole formation proceeds via a novel nitrogen to carbon migration of the carboalkoxy group.  相似文献   
8.
A uracil‐based heterocyclic azo derivative was prepared by coupling diazotized 5‐aminouracil with 2‐naphthol. This ligand, viz., 1‐(2,4‐dioxopyrimidine‐5‐yl)‐azo‐naphth‐2‐ol (HNAP), was used as a precursor for the synthesis of a series of complexes with manganese(II), cobalt(II), nickel(II), copper(II), and zinc(II) ions. Various physicochemical measurements UV–Visible, Infrared (IR), 1H NMR, 13C Nuclear Magnetic Resonance (NMR), and electron spin resonance (ESR) spectral studies were employed to characterize the ligand and the metal complexes. The ligand showed good selectivity toward Mn2+ over the other metal ions with a detection limit of 1.36 μM. This probe was used for the confocal fluorescence imaging of Mn2+ ions in Michigan Cancer Foundation‐7 (MCF‐7) cells. The ligand and the metal complexes were tested for their cytotoxicity on the MCF‐7 cell line. It was observed that complexation of HNAP with the metal ions exhibited a promising cytotoxicity.  相似文献   
9.
10.
Photocatalytic action of the commercial TiO2 was the subject of study on the destruction of the microbes within the biofilms. The TiO2 powder was characterized by X-ray diffraction (XRD) for identifying its type and the particle size was determined. The biofilm was allowed to form over TiO2 coatings over glass slides irradiated with polychromatic light for different time durations and distances. It indicates that a five-fold decrease in bacterial count due to the formation of H2O2 at TiO2/biofilm interface. The formation of H2O2 at the TiO2/biofilm interface is estimated and it does not destroy the entire bacterial population within the biofilm. Bacterial killing effect is supported by FT-IR analysis.  相似文献   
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