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661.
We study the effects of jet quenching on the hydrodynamical evolution of the quark-gluon plasma (QGP) fluid created in a heavy-ion collision. In jet quenching, a hard QCD parton, before fragmenting into a jet of hadrons, deposits a fraction of its energy in the medium, leading to suppressed production of high-pT hadrons. Assuming that the deposited energy quickly thermalizes, we simulate the subsequent hydrodynamic evolution of the QGP fluid. For partons moving at supersonic speed, vp>cs, and sufficiently large energy loss, a shock wave forms leading to conical flow. The PHENIX Collaboration recently suggested that observed structures in the azimuthal angle distribution might be caused by conical flow. We show here that, for phenomenologically acceptable values of parton energy loss, conical flow effects are too weak to explain these structures. 相似文献
662.
Chaudhuri S Chupas P Morgan BJ Madden PA Grey CP 《Physical chemistry chemical physics : PCCP》2006,8(43):5045-5055
Cubic nanoparticles of alpha-AlF(3) containing 864 and 2048 atoms were investigated by using molecular dynamics simulations. Significant structural rearrangements of these particles occurred, primarily at the edges and corners of the particles, and 3 and 5 membered (Al-F-)(n) ring structures were observed in addition to the 4-membered rings seen in bulk alpha-AlF(3). These 3 and 5 membered ring structures are, however, present in other metastable forms of AlF(3), which are formed at low temperatures from high surface area precursors. The surfaces of the nanoparticles were very dynamic on the timescale of the MD run, Al-F bonds being continually broken and formed, resulting in the movement of the low coordinate Lewis acid Al sites on the surfaces of the particles. The Lewis acid sites, which represent the catalytically active sites for F/Cl exchange reactions, are largely present at the corners and edges of the particles. The particles show larger rhombohedral distortions than present in the bulk phase and do not undergo a rhombohedral to cubic phase transition at elevated temperatures. The results are compared with pair distribution function (PDF) analysis results from fluorinated gamma-Al(2)O(3), nanoparticles of AlF(3) prepared by plasma routes and alpha- and beta-AlF(3). Broad peaks between 3.3 and 4.5 A in the PDF plots of the fluorinated Al(2)O(3) and the nanoparticles indicate a distribution of Al-F distances arising from Al and F atoms in connected AlF(6) octahedra; this is consistent with the presence of ring structures other than those found in alpha-AlF(3). 相似文献
663.
Aubry C Wilson AJ Jenkins PR Mahale S Chaudhuri B Maréchal JD Sutcliffe MJ 《Organic & biomolecular chemistry》2006,4(5):787-801
We present the design, synthesis, and biological activity of three classes of tryptamine derivatives, which are non-planar analogues of the toxic anti-cancer agent fascaplysin. We show these compounds to be selective inhibitors of CDK4 over CDK2, the most active compound has an IC50 for the inhibition of CDK4 of 6 microM. 相似文献
664.
García MD Wilson AJ Emmerson DP Jenkins PR Mahale S Chaudhuri B 《Organic & biomolecular chemistry》2006,4(24):4478-4484
The design, synthesis and biological activity of a series of non-planar dihydro-beta-carboline and beta-carboline-based derivatives of the toxic anticancer agent fascaplysin is presented. We show these compounds to be selective inhibitors of CDK4 over CDK2 with an IC50 (CDK4-cyclin D1) = 11 micromol for the best compound in the series 4d. The crystallographic analysis of some of the compounds synthesised (3b/d and 4a-d) was carried out, in an effort to estimate the structural similarities between the designed inhibitors and the model compound fascaplysin. 相似文献
665.
Pal Chaudhuri U Whiteaker LR Yang L Houser RP 《Dalton transactions (Cambridge, England : 2003)》2006,(15):1902-1908
Copper complexes of a family of pyridylmethylamide ligands HL(Ph), HL(Me3) and HL(Ph3) were synthesized and characterized [HL(Ph) = 2-phenyl-N-(2-pyridylmethyl)acetamide; HL(Me3) = 2,2-dimethyl-N-(2-pyridylmethyl)propionamide; HL(Ph3) = 2,2,2-triphenyl-N-(2-pyridylmethyl)acetamide]. The reaction of copper(II) salts with the HL family and triethylamine in methanol yields copper(II) complexes [Cu4(L(Ph))4(OH)2](ClO4)2 (1), [Cu2(HL(Me3))2(OMe)2(MeOH)2](OTf)2 (2) and [Cu2(HL(Ph3))2(OMe)2(MeOH)2](OTf)2 (3). The complexes have different nuclearity owing to varying steric properties of the ligands used. Complex 1 self-assembles in the presence of excess base to form a tetranuclear complex. Complexes 2 and 3 are binuclear and are bridged by a pair of methoxide ligands. Steric encumbrance of the ligands in 2 and 3 prevent cluster formation. 相似文献
666.
Chaudhuri P Wagner R Khanra S Weyhermüller T 《Dalton transactions (Cambridge, England : 2003)》2006,(41):4962-4968
Reaction of a 1 : 1 : 1 molar ratio of NiCl(2), NaN(3) and H(2)L, a tetradentate ligand N-(2-pyridyl)methyl)-N,N-bis(2'-hydroxy-3',5'-dimethylbenzyl)amine in methanol in presence of Et(3)N results in a turquoise precipitate, which affords deep green crystals of [Ni(2)(HL)(2)(N(3))(2)]*1.5CH(2)Cl(2) (1) and [Ni(2)(HL)(2)(N(3))(2)]*H(2)O (2) upon crystallization from CH(2)Cl(2)-MeOH or THF-MeOH, respectively. Both complexes reveal distorted octahedral NiN(4)O(2) coordination environments around the Ni(ii) centers with bis(micro-1,1-azido) bridging ligands. Complex 1 displays an unprecedented small Ni-N-Ni bridge angle of 90.4 degrees , whereas 2 contains the said angle of av. 98.7 degrees lying in the usual range observed for other comparable structures. The variable-temperature magnetic susceptibility together with the variable-field, variable-temperature (VTVH) magnetization measurements discern different ground states of S(t) = 0 for 1 and S(t) = 2 for 2. The magnetic behaviours of these compounds are discussed in the context of the known bis(end-on azido) bridging dinickel(II) complexes. 相似文献
667.
One-dimensional ZnO nanostructure arrays such as nanowires, nanonails, and nanotrees, have been synthesized by oxygen assisted thermal evaporation of metallic zinc on a quartz substrate over a large area. Morphological evolution of ZnO nanostructures at different time scales and different positions of the substrates have been studied by electron microscopy. A self-catalyzed vapor-liquid-solid (VLS) process is believed to be responsible for the nucleation and subsequently a vapor-solid process is operative for further longitudinal growth. The photoluminescence spectrum showed a weak UV and a broad green emission peak at 3.25 and 2.49 eV, respectively. The latter was attributed to the presence of zinc interstitial defects. Electrical resistivity as a function of temperature showed activated mechanisms to be present. The electrical response of the ZnO nanonail arrays to different gases (CO, NO2, and H2S) indicated that there could be possible application as gas sensors for this material. 相似文献
668.
Nanostructures of ZnS, both particles and rods, were synthesized through solvothermal processes and characterized by x-ray diffraction and high resolution transmission electron microscopy. Positron lifetime and Doppler broadening measurements were made to study the features related to the defect nanostructures present in the samples. The nanocrystalline grain surfaces and interfaces, which trapped significant fractions of positrons, gradually disappeared during grain growth, as indicated by the decreasing fraction of orthopositronium atoms. The crystal vacancies present within the grains also trapped positrons. These vacancies further agglomerated into clusters during the thermal treatment given to effect grain growth. The positron lifetime was remarkably large at extremely small grain sizes (approximately 1.5 nm) and this was attributed to the occurrence of quantum confinement effects, as verified through optical absorption measurements. Positron lifetimes in ZnS nanorods increased with increasing content of cubic phase in the samples and this observation is assigned to the annihilation of positrons in sites with increased cubic unit cell volume. The Doppler broadened spectra also indicated qualitative changes consistent with these observations. 相似文献
669.
The probabilistic roadmap algorithm is a leading heuristic for robot motion planning. It is extremely efficient in practice, yet its worst case convergence time is unbounded as a function of the input's combinatorial complexity. We prove a smoothed polynomial upper bound on the number of samples required to produce an accurate probabilistic roadmap, and thus on the running time of the algorithm, in an environment of simplices. This sheds light on its widespread empirical success. 相似文献
670.
Naresh B. Kotadiya Anjana J. Kothari Devendra Tiwari Tapas K. Chaudhuri 《Applied Physics A: Materials Science & Processing》2012,108(4):819-824
A chemical bath deposition method of preparing photoconducting nanocrystalline lead sulphide (PbS) thin films at room temperature (RT) is described. The aqueous bath of lead acetate, thiourea, and ammonium hydroxide produce films of about 100?nm thicknesses in 45?minutes. X-ray diffraction (XRD) studies show that these films are nanocrystalline cubic PbS with 10?nm crystallite size. Atomic Force Microscope (AFM) and Scanning Electron Microscope (SEM) revealed that the films consist of spherical grains of sizes 100 to 200?nm. The transmission spectra of the films show onset of absorption edge around 850?nm and the bandgap is around 1.65?eV. The films are p-type with dark conductivity of 2.5×10?3?S/cm and mobility of 0.07?cm2/V?s. The photosensitivity is 6–7 for an illumination of 80?mW/cm2 from a halogen lamp (50?W, 12?V). Transient photoconductivity measurements reveal short and long life times of minority carriers. Thermoelectric and photothermoelectric studies show that photoconductivity in these films is mainly due to photogenerated majority carriers. 相似文献