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排序方式: 共有73条查询结果,搜索用时 0 毫秒
1.
K. C. Kumara Swamy E. Balaraman M. Phani Pavan N. N. Bhuvan Kumar K. Praveen Kumar N. Satish Kumar 《Journal of Chemical Sciences》2006,118(6):495-501
The diversity of products in the reaction of diethyl azodicarboxylate (DEAD)/diisopropyl azodicarboxylate (DIAD) and activated
acetylenes with PIII compounds bearing oxygen or nitrogen substituents is discussed. New findings that are useful in understanding the nature
of intermediates involved in the Mitsunobu reaction are highlighted. X-ray structures of two new compounds (2-t-Bu-4-MeC6H3O)P (μ-N-t-Bu)2P+[(NH-t-Bu)N[(CO2]-i-Pr)(HNCO2-i-Pr)]](Cl-)(2-t-Bu-4-MeC6H3OH)(23)and [CH2(6-t-Bu-4-Me-C6H2O)2P(O)C(CO2Me)C-(CO2Me)CClNC(O)Cl] (33) are also reported. The structure of23 is close to one of the intermediates proposed in the Mitsunobu reaction. 相似文献
2.
Subash C. Raghu Sheela Berchmans Dr. Kanala L. Phani Dr. Venkatraman Yegnaraman Dr. 《化学:亚洲杂志》2007,2(6):775-781
This paper describes the formation of catalytically active thin films of Pt, Pt/Au, and Pt/Ru on gold substrates stabilized by amine‐terminated polyamidoamine (PAMAM) dendrimers. A monolayer of dendrimer is initially self‐assembled on the gold substrate, which serves as a template for the growth of catalytically active thin films. As dendrimers contain tens to hundreds of functional groups at the periphery, the aggregate strength of the multidentate interactions with the gold substrate leads to the formation of robust films. The films were found to exhibit high catalytic activity for the oxidation of small hydrocarbons such as methanol. Such films offer versatility and scope for the design of effective electrocatalysts, especially in the context of microfuel cells and “dendrichips”; hence, they could find applications in the fields of sensors, fuel cells, and waste‐water treatment. 相似文献
3.
M. Jayalakshmi P. Radhika K. Phani Raja M. Mohan Rao 《Journal of Solid State Electrochemistry》2007,11(2):165-172
Nanoparticles of α-phase nickel hydroxide were synthesized by a single-step hydrothermal method using urea as the hydrolytic agent. Precipitated powders were of pure turbostratic α-phase as confirmed by x-ray diffraction profile. The ageing of α-Ni(OH)2 in 1.0 M alkali solutions is investigated for pure non-intercalated α-Ni(OH)2 and thiourea intercalated/absorbed α-phase nanomaterials. The α-Ni(OH)2 powder immobilized on the surface of graphite electrodes shows a gradual α→β phase transformation with continuous voltammetric cycling, and the concentration gradient of water that exists in the layered-double-hydroxide-like interlayers of α-phase and the solution was shown to play a crucial role on the high electrochemical activity of this phase nickel hydroxide. To understand the role of water in the ageing process, concomitant entries of non-aqueous solvents like ethanol and acetonitrile along with thiourea were effected. Cyclic voltammetric measurements of thiourea-treated α-Ni(OH)2 samples revealed that hydroxyl ion influx during the anodic oxidation depends on the counter flux of solvent molecules, and if the intercalated the solvent is acetonitrile, then the electrochemical activity of α-Ni(OH)2 reduced drastically; Q
a/Q
c>1 for water as solvent in the interlayers α-Ni(OH)2 and Q
a/Q
c<1 for ethanol and acetonitrile as solvents. The α-phase gets stabilized in the presence of thiourea with water and ethanol as co-intercalates. Transmission electron microscope images of α-Ni(OH)2 and thiourea-treated samples show a change in particle size and morphology. Elemental CHNS analysis confirms the presence of sulphur in the thiourea intercalated samples. 相似文献
4.
Pitchiah Esakki Karthik Chinnaiah Jeyabharathi Shanmugam Senthil Kumar Kanala Lakshmi Narasimha Phani 《Journal of Solid State Electrochemistry》2013,17(12):3055-3061
It is shown that the gold surface is catalytically deactivated and smoothened upon removal of the Prussian blue (PB)–gold nanocomposite formed on the gold surface. Atomic force microscopy proves surface smoothening after PB removal. The voltammetric responses of Ru(NH3)6Cl3 on the smoothened surface remain unaffected, but the reactions that involve multistep and inner-sphere electron transfer are affected on the smoothened surface as exemplified by hydroquinone, ferrous oxalate redox reactions, and oxygen reduction. These effects are attributed to catalytic deactivation as a consequence of removal of the active sites. Figure
It is shown that the gold surface is catalytically deactivated and smoothened upon removal of the Prussian blue (PB)–gold nanocomposite formed on the gold surface. Atomic force microscopy proves surface smoothening after PB removal. The voltammetric responses of Ru(NH3)6.Cl3 on smoothened surface remain unaffected, but the reactions that involve multistep and inner-sphere electron transfer are affected on the smoothened surface as exemplified by hydroquinone, ferrous oxalate redox reactions, and oxygen reduction. These effects are attributed to catalytic deactivation as a consequence of removal of the active sites. Graphical abstract shows the Au surface smoothening as a consequence of Prussian blue-gold nanocomposite (Au-PB) formation and removal 相似文献
5.
6.
This paper is concerned with the experimental evaluation of the performance of viscous damping identification methods in linear vibration theory. Both existing and some new methods proposed by the present authors [A.S. Phani, J. Woodhouse, Viscous damping identification in linear vibration, Journal of Sound and Vibration 303 (3–5) (2007) 475–500] are applied to experimental data measured on two test structures: a coupled three cantilever beam with moderate modal overlap and a free–free beam with low modal overlap. The performance of each method is quantified and compared based on three norms and the best methods are identified. The role of complex modes in damping identification from vibration measurements is critically assessed. 相似文献
7.
8.
S. N. V. M. S. Gupta A. K. Nayak U. B. Misra Balaji Rao Yarasi C. Phani Babu G. Kalyanakrishnan 《Journal of Radioanalytical and Nuclear Chemistry》2017,313(3):571-579
The present paper describes a new analytical method developed for direct determination of boron in steels using radio frequency glow discharge optical emission spectrometer. “Single parameter alternative method” technique has been used to optimize the various experimental conditions of glow discharge plasma such as forward power, gas pressure inside plasma chamber, pre-integration time, and integration time. Different emission lines for boron were studied and inter element interference effect is also discussed in the paper. A complete statistical analysis has been done to validate the developed method. A RSD of less than ±5% is achieved for boron in the range of 0.0010–0.020% in Steels using this method. 相似文献
9.
Babu Rao Chandu Sreekanth Nama Kanchanamala Kanala Balasekhara Reddy Challa Rihana Parveen Shaik Mukkanti Khagga 《Analytical and bioanalytical chemistry》2010,398(3):1367-1374
A novel simple, sensitive, selective, and rapid high-performance liquid chromatography coupled with tandem mass spectrometry
method was developed and validated for quantification of riluzole in human plasma. The chromatography was performed by using
a Zorbax-SB-C18 (4.6 × 75 mm, 3.5 μm) column , isocratic mobile phase 0.1% formic acid/acetonitrile (10:90 v/v), and an isotope-labeled
internal standard (IS), [13C,15N2]riluzole. The extraction of drug and internal standard was performed by liquid–liquid extraction and analyzed by MS in the
multiple reaction monitoring (MRM) mode using the respective [M+H]+ ions, m/z 235.0/165.9 for riluzole and m/z 238.1/169.0 for the IS. The calibration curve was linear over the concentration range 0.5–500.0 ng/ml for riluzole in human
plasma. The limit of quantification (LOQ) was demonstrated at 0.5 ng/ml. The within-batch and between-batch precision were
0.6–2.3% and 1.4–5.7%, and accuracy was 97.1–101.1% and 98.8–101.2% for riluzole respectively. Drug and IS were eluted within
3.0 min. The validated method was successfully applied in a bioequivalence study of riluzole in human plasma. 相似文献
10.
Yan Zhang Phani Morisetti Jeffery Kim Lynelle Smith Hai Lin 《Theoretical chemistry accounts》2008,121(5-6):313-319
Theoretical studies are presented into the experimentally observed regioselectivity difference of testosterone hydroxylation by cytochrome P450 3A4 at the 1β, 2β, 6β, and 15β positions. Such regioselectivity is investigated by density functional theory calculations on a model system. The barrier heights of hydrogen abstraction, which are corrected by zero-point vibrational energies, are computed to be about 10.1, 13.6, 14.4, and 16.2 kcal/mol for the 6β-, 2β-, 15β-, and 1β-positions, respectively. The calculated barriers suggest the regioselectivity preference of 6β ? 2β > 15β > 1β, which is in good agreement with experimental findings. 相似文献