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排序方式: 共有122条查询结果,搜索用时 15 毫秒
1.
R. Nagarajan S. Ayyappan C. N. R. Rao 《Physica C: Superconductivity and its Applications》1994,220(3-4):373-376
While YSr2Cu3O7 cannot be prepared under ambient conditions, partial substitution of the phosphate group for copper, as in YSr2Cu2.8(PO4)0.2Oy, stabilizes this phase in the orthorhombic structure, but the material is not superconducting. Superconductivity in YSr2Cu2.8(PO4)0.2Oy is obtained by increasing the hole concentration through partial substitution of Y by Ca, as in Y0.7Ca0.3Sr2Cu2.8(PO4)0.2Oy (Tc≈40 K). By incorporating the phosphate group in orthorhombic YBaSrCu3O 7, a stable tetragonal derivative of the formula YBaSrCu2.8(PO4)0.2Oy (Tc≈ 47 K) has been prepared; the Tc increases to 70 K by partial substitution of Y by Ca as in Y0.7Ca0.3BaSrCu2.8(PO4)0.2Oy. 相似文献
2.
A. Subbiah Pandi V. Rajakannan D. Velmurugan Masood Parvez Moon‐Jib Kim A. Senthilvelan S. Narasinga Rao 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):o164-o167
N‐(2‐Chlorobenzyl)‐1,2,3,4‐tetrahydroisoquinoline‐1,3‐dione, C16H12ClNO2, crystallizes in P21/n with three crystallographically independent molecules in the asymmetric unit, which differ slightly in conformation, N‐(2‐bromo‐4‐methylphenyl)‐1,2,3,4‐tetrahydroisoquinoline‐1,3‐dione, C16H12BrNO2, crystallizes in P21/n with one molecule in the asymmetric unit andN‐(2,3‐dichlorophenyl)‐1,2,3,4‐tetrahydroisoquinoline‐1,3‐dione, C15H9Cl2NO2, crystallizes in P21/c with one molecule in the asymmetric unit. In all three structures, the heterocyclic rings adopt approximately planar conformations. The pyridine rings are orthogonal to the substituted phenyl rings. In all three structures, the crystal packing is stabilized by intermolecular C—H?O hydrogen bonds. 相似文献
3.
Amphiphilic and hydrophilic oligomers were synthesized and coated on fused silica capillaries using a sol-gel technique. Sol-gel-coated capillaries were evaluated for the solid-phase microextraction and preconcentration of a wide variety of non-polar and polar analytes. Both types of coatings were stable under high temperature (up to 280 degrees C). The extraction efficiency of the sol-gel coatings was evaluated for the extraction of both non-polar and polar analytes, including organochlorine pesticides, triazine herbicides, estrogens and alkylphenols (APs) and bisphenol-A (BPA). Compared with commercially available solid-phase microextraction (SPME) adsorbents such as poly(dimethylsiloxane)divenylbenzene and polyacrylate, the new materials showed comparable selectivity and sensitivity towards both non-polar and polar analytes. The new coatings gave good linearity and detection limits. For example with triazines, a detection limit of <0.005 microl l(-1), precision from 5.0 to 11.0% (n = 6) and linearity of the calibration plots (0.5 to 50 microl l(-1)) were obtained. The sol-gel coated SPME capillaries were used for the determination of triazine herbicides in reservoir water samples collected in Singapore. 相似文献
4.
Three-dimensional open frameworks [Co2(nicotinate)4(mu-H2O)]-CH3CH2OH-H2O, 1, and [Ni2(nicotinate)4(mu-H2O)]-CH3CH2OH-H2O, 2, were obtained by hydro(solvo)thermal reactions between 3-cyanopyridine and cobalt(II) nitrate and nickel(II) perchlorate, respectively. Both 1 and 2 exhibit complicated 3-D structures based on [M2(nicotinate)4(mu-H2O)] (M = Co or Ni) building blocks and possess open channels that are occupied by removable solvent molecules. 3-D open frameworks [M2L4(mu-H2O)]-HL-(H2O)x (where M = Co, x = 2, 3, and M = Ni, x = 1, 4, and L = trans-3-(3-pyridyl)acrylate) were similarly prepared with trans-3-(3-pyridyl)acrylic acid in place of 3-cyanopyridine. Compounds 3 and 4 are isostructural and exhibit network topologies similar to that of 1 with open channels occupied by disordered trans-3-(3-pyridyl)acrylic acid and water guest molecules. Crystal data for 1: triclinic space group Ponebar, a = 10.534(1) A, b = 11.907(1) A, c = 14.046(1) A, alpha = 106.645(1) degrees, beta = 101.977(1) degrees, gamma = 112.078(1) degrees, and Z = 4. Crystal data for 2: tetragonal space group P4/ncc, a = 20.089(1) A, c = 14.016(1) A, and Z = 4. Crystal data for 3: monoclinic space group C2/c, a = 14.082(2) A, b = 15.278(2) A, c = 18.537(2) A, beta = 105.360(2) degrees, and Z = 2. Crystal data for 4: monoclinic space group C2/c, a = 14.082(1) A, b = 15.250(1) A, c = 18.606(1) A, beta = 106.747(1) degrees, and Z = 2. 相似文献
5.
Manickam Amsaveni Ayyappan Anumary Meiyazhagan Ashokkumar Bangaru Chandrasekaran Palanisamy Thanikaivelan 《Applied biochemistry and biotechnology》2013,171(6):1500-1512
Collagen (C) and cellulose are prominent biopolymers from the animal and plant kingdom and widely used in bioengineering. Albumin, on the other hand, is the most abundant plasma protein present in mammalian blood. In this work, collagen extracted from animal skin waste was blended with hydroxyethyl cellulose (HEC) and bovine serum albumin (A) and wet-spun to form hybrid biodegradable C/HEC/A fibers. They were further cross-linked with glutaraldehyde vapors and analyzed. X-ray diffraction and infra-red spectroscopic studies of the hybrid fibers display peaks corresponding to collagen, cellulose, and albumin. Incorporation of cellulose into the biopolymeric matrix leads to a reasonable improvement in mechanical, swelling, and thermal properties of hybrid fibers. Addition of albumin improves the regularity of fiber surface without altering the porosity as observed under a microscope. Hence, the formed hybrid biofibers can be potentially used as a suture material as well as for different biomedical applications due to their improved properties. 相似文献
6.
Palanisamy Jamuna Rani Subbiah Thirumaran Samuele Ciattini 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):778-789
Abstract Six new nickel complexes of two dithiocarbamate ligands (cyfdtc = N-cyclohexyl-N- furfuryldithiocarbamate and bztpedtc = N-benzyl-N-[2-thiophenylethyl]dithiocarbamate) namely, (Ni[cyfdtc]2) (1), (Ni[bztpedtc]2) (2), (Ni[cyfdtc][NCS][PPh3]) (3), (Ni[bztpedtc] [NCS][PPh3]) (4), (Ni[cyfdtc][PPh3]2)ClO4 (5), and (Ni[bztpedtc][PPh3]2)ClO4 (6) have been prepared and characterized using IR, electronic, and NMR (1H and 13C) spectra. A single crystal X-ray structural analysis was carried out for complex 3 and showed that nickel is in a distorted square planar arrangement with the NiS2PN chromophore. The shift in νC?N of the heteroleptic complexes to higher frequencies compared with the parent complex is assigned to mesomeric delocalization of electron density from the dithiocarbamate ligand toward the metal atom, which increases the contribution of polar thioureide form in mixed ligand complexes. Electronic spectral studies suggest square planar geometry for the complexes. In the 13C NMR spectra, the upfield shift of NCS2 carbon signal for 3 and 4 from the chemical shift value of 1 and 2 is due to effect of PPh3 on the mesomeric drift of electron density toward nickel throughout thioureide C?N bond. 相似文献
7.
8.
Subbiah Meenakshisundaram RM. Sockalingam 《Journal of molecular catalysis. A, Chemical》2000,160(2):269-275
Catalytic activity of Os(VIII) in the oxidation of some twenty organic sulfides with sodium salt of N-chlorobenzenesulfonamide (CAB) has been investigated in alkaline (pH8.7) t-butanol–water (1:1 v/v) medium. Significant retarding influence of [OH−] on the reactivity is exhibited. The catalysed reaction is strongly accelerated in the presence of Hg(II). Imperfections are observed in the linear Hammett relationship in the case of –NO2 substituents. 相似文献
9.
10.
Thathan Premkumar Subbiah Govindarajan 《Journal of Thermal Analysis and Calorimetry》2010,100(2):725-732
The new hydrazinium lanthanide metal complexes of 2-pyrazinecarboxylic acid (HpyzCOO) of the formulae (N2H5)2[Ln(pyzCOO)5] · 2H2O (1), where Ln = La or Ce and (N2H5)3[Ln(pyzCOO)4(H2O)] · 2NO3 (2), where Ln = Pr, Nd, Sm or Dy have been synthesized and characterized by physico-chemical methods. The IR absorption bands
of N–N stretching at 960 cm−1 unambiguously prove the existence of N2H5
+ ions. The bonding parameters β, b1/2, % δ and η, have been calculated from the electronic spectroscopic (hypersensitive) bands of Pr(III) and Nd(III) complexes.
All the complexes undergo endothermic followed by exothermic decomposition to leave the respective metal oxides as the end
products. However, the DTA of the complexes 2 demonstrate rather sharp peak than the complexes 1, owing to overwhelming exothermicity, which may be due to the loss of both hydrazine and nitrate moieties in the same step.
The X-ray powder diffraction studies reveal the existence of isomorphism among the member complexes. 相似文献