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561.
Cation distribution in quenched and furnace-cooled samples of composition NixM1?xFe2O4 (where M is either Mg2+ or Cu2+) has been studied through magnetization measurements. It has been found that cation distribution in these mixed ferrites cannot be predicted by site preference energies. In magnesium-nickel ferrites, cation distribution is controlled by heat treatment up to x = 0.5, beyond which the effect of heat treatment diminishes. Addition of Ni2+ ions in copper ferrite reduces the diffusibility of Cu2+ ions and the distribution tends toward inverse spinel in the high-nickel region. 相似文献
562.
The reaction of alkenylalanes with mercuric chloride in THF produces stereospecically the coresponding alkenylmercuric chlorides in high yields. 相似文献
563.
In a previous communication, we showed that a single Au atom behaves like H in its bonding to Si in a series of Si-Au clusters, SiAu(n) (n = 2-4) (Kiran et al. Angew. Chem., Int. Ed. 2004, 43, 2125). In this article, we show that the H analogy of Au is more general. We find that the chemical bonding and potential energy surfaces of two disilicon Au clusters, Si(2)Au(2) and Si(2)Au(4), are analogous to Si(2)H(2) and Si(2)H(4), respectively. Photoelectron spectroscopy and ab initio calculations are used to investigate the geometrical and electronic structures of Si(2)Au(2)(-), Si(2)Au(4)(-), and their neutral species. The most stable structures for both Si(2)Au(2) and Si(2)Au(2)(-) are found to be C(2)(v), in which each Au bridges the two Si atoms. For Si(2)Au(4)(-), two nearly degenerate dibridged structures in a cis (C(2)(h)) and a trans (C(2)(v)) configuration are found to be the most stable isomers. However, in the neural potential energy surface of Si(2)Au(4), a monobridged isomer is the global minimum. The ground-state structures of Si(2)Au(2)(-) and Si(2)Au(4)(-) are confirmed by comparing the computed vertical detachment energies with the experimental data. The various stable isomers found for Si(2)Au(2) and Si(2)Au(4) are similar to those known for Si(2)H(2) and Si(2)H(4), respectively. Geometrical and electronic structure comparisons with the corresponding silicon hydrides are made to further establish the isolobal analogy between a gold atom and a hydrogen atom. 相似文献
564.
Ravi Kiran Kaja K. V. Surendranath P. Radhakrishnanand P. V. V. Satyanarayana 《Chromatographia》2009,69(11-12):1407-1412
A novel, sensitive, stability indicating RP-LC method has been developed for the quantitative determination of mitotane, its impurity in both bulk drugs and pharmaceutical dosage forms. Efficient chromatographic separation was achieved using a C18 stationary phase with simple mobile phase combination delivered in an isocratic mode and quantitation was by ultraviolet detection at a wavelength of 230 nm. The mobile phase consisted of buffer and acetonitrile (25:75, v/v) delivered at a flow rate of 1.0 mL min?1. Buffer consisted of 10 mM potassium dihydrogen orthophosphate monohydrate, pH adjusted to 2.5 by orthophosphoric acid. In the developed LC method the resolution (R s ) between mitotane and its impurity namely Imp-1 was found to be greater than 2.5. Regression analysis shows an r value (correlation coefficient) greater than 0.999 for mitotane and its impurity. This method was capable to detect the impurity of mitotane at a level of 0.003% with respect to test a concentration of 0.2 mg mL?1 for a 10 μL injection volume. The inter- and intra-day precision values for mitotane and its impurity was found to be within 2.0% RSD. The method has shown good and consistent recoveries for mitotane in bulk drugs (99.2–101.5%), pharmaceutical dosage forms (98.2–103.1%) and for its impurity (99.7–102.1%). The test solution was found to be stable in diluent for 48 h. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. Considerable degradation was found to occur in basic stress hydrolysis. The stress samples were assayed against a qualified reference standard and the mass balance was found close to 99.97%. The developed RP-LC method was validated with respect to linearity, accuracy, precision and robustness. 相似文献
565.
David Alvarez Kiran Chatty Michel J. Abou-Khalil Robert Gauthier Ralph Halbach 《Microelectronics Reliability》2009,49(12):1417-1423
Decrease of the drain silicide-blocking-to-gate spacing in gate-silicided-ESD-NMOSFETs improves the TLP and HBM failure levels up to 30%, while no effect is observed when decreasing the source silicide-blocking-to-gate spacing. Failure analysis and simulation results show that current crowding in the drain silicide region accounts for the difference in failure current for the devices. 相似文献
566.
567.
Kiran Ramesh Ashok Gopalarathnam Jack R. Edwards Michael V. Ol Kenneth Granlund 《Theoretical and Computational Fluid Dynamics》2013,27(6):843-864
An inviscid theoretical method that is applicable to non-periodic motions and that accounts for large amplitudes and non-planar wakes (large-angle unsteady thin airfoil theory) is developed. A pitch-up, hold, pitch-down motion for a flat plate at Reynolds number 10,000 is studied using this theoretical method and also using computational (immersed boundary method) and experimental (water tunnel) methods. Results from theory are compared against those from computation and experiment which are also compared with each other. The variation of circulatory and apparent-mass loads as a function of pivot location for this motion is examined. The flow phenomena leading up to leading-edge vortex shedding and the limit of validity of the inviscid theory in the face of vortex-dominated flows are investigated. Also, the effect of pitch amplitude on leading-edge vortex shedding is examined, and two distinctly different vortex-dominated flows are studied using dye flow visualizations from experiment and vorticity plots from computation. 相似文献
568.
Kiran Chinthapally Nicholas P. Massaro Sabrina Ton Eric D. Gardner Indrajeet Sharma 《Tetrahedron letters》2019,60(46):151253
A rhodium carbenoid initiated cascade has been developed for the stereoselective synthesis of medium-sized azacycles. The cascade approach utilizes readily accessible N-benzyl protected aminochalcones and vinyldiazo compounds to access 9-membered azacycles through a carbene- nitrogen insertion/aldol/oxy-Cope sequence. The cascade reaction has proven general with a range of N-benzyl protected aminochalcones and vinyldiazos to provide diverse medium-sized azacycles. 相似文献
569.
Christopher T. Lohans H. T. Henry Chan Tika R. Malla Kiran Kumar Jos J. A. G. Kamps Darius J. B. McArdle Emma vanGroesen Mariska deMunnik Catherine L. Tooke James Spencer Robert S. Paton Jürgen Brem Christopher J. Schofield 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(7):2012-2016
Enzymes often use nucleophilic serine, threonine, and cysteine residues to achieve the same type of reaction; the underlying reasons for this are not understood. While bacterial d,d ‐transpeptidases (penicillin‐binding proteins) employ a nucleophilic serine, l,d ‐transpeptidases use a nucleophilic cysteine. The covalent complexes formed by l,d ‐transpeptidases with some β‐lactam antibiotics undergo non‐hydrolytic fragmentation. This is not usually observed for penicillin‐binding proteins, or for the related serine β‐lactamases. Replacement of the nucleophilic serine of serine β‐lactamases with cysteine yields enzymes which fragment β‐lactams via a similar mechanism as the l,d ‐transpeptidases, implying the different reaction outcomes are principally due to the formation of thioester versus ester intermediates. The results highlight fundamental differences in the reactivity of nucleophilic serine and cysteine enzymes, and imply new possibilities for the inhibition of nucleophilic enzymes. 相似文献
570.
Wireless Personal Communications - In this paper, a triangular complementary split ring resonator (TCSRR) based compact metamaterial antenna for multiband operation is presented. TCSRR is used to... 相似文献