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1.
We report on further developments in the three-dimensional tracking of a particle deep within the tumbling ball charge of
an experimental mill. The experimental X-ray program employing the use of bi-planar X-ray angiography now includes the tracking
of a typical 6 mm bulk charge particle in three dimensions with a spatial resolution that is accurate to within 0.15 mm. The
improved experimental tracking techniques presented were developed for the purpose of generating accurate three-dimensional
particle trajectory data against which to validate a numerical method for the simulation of discrete media, namely the discrete
element method (DEM). These improvements are complimented with techniques for comparing charge profiles between numerical
DEM simulations and three-dimensional experimental trajectory data. 相似文献
2.
Rosenthal SJ Tomlinson I Adkins EM Schroeter S Adams S Swafford L McBride J Wang Y DeFelice LJ Blakely RD 《Journal of the American Chemical Society》2002,124(17):4586-4594
To explore the potential for use of ligand-conjugated nanocrystals to target cell surface receptors, ion channels, and transporters, we explored the ability of serotonin-labeled CdSe nanocrystals (SNACs) to interact with antidepressant-sensitive, human and Drosophila serotonin transporters (hSERT, dSERT) expressed in HeLa and HEK-293 cells. Unlike unconjugated nanocrystals, SNACs were found to dose-dependently inhibit transport of radiolabeled serotonin by hSERT and dSERT, with an estimated half-maximal activity (EC(50)) of 33 (dSERT) and 99 microM (hSERT). When serotonin was conjugated to the nanocrystal through a linker arm (LSNACs), the EC(50) for hSERT was determined to be 115 microM. Electrophysiology measurements indicated that LSNACs did not elicit currents from the serotonin-3 (5HT(3)) receptor but did produce currents when exposed to the transporter, which are similar to those elicited by antagonists. Moreover, fluorescent LSNACs were found to label SERT-transfected cells but did not label either nontransfected cells or transfected cells coincubated with the high-affinity SERT antagonist paroxetine. These findings support further consideration of ligand-conjugated nanocrystals as versatile probes of membrane proteins in living cells. 相似文献
3.
J.M. McBride 《Tetrahedron》1974,30(14):2009-2022
The correct quinoid structure for the dimer of triphenylmethyl radicals was proposed in 1904. By 1906 there existed three independent lines of evidence which support this structure: acid-catalyzed aromatization, para-halogen lability, and radical chain autoxidation. Despite this evidence, and the skill and insight of the numerous chemists who studied the system, the incorrect hexaphenylethane structure was assigned to the dimer until 1968. This paper attempts to explain how this could have happened by tracing the evolution of triphenylmethyl theory and of attitudes toward the evidence from 1900 until 1968. 相似文献
4.
5.
H.C. Clark S.S. McBride N.C. Payne C.S. Wong 《Journal of organometallic chemistry》1979,178(2):393-408
The reaction of [Pt((F3C)CCH(CF3))(P(C2H5)3)2CH3OH]PF6 with allene in methanol affords a novel metallocyclic ethereal complex [CH3)(P(C2H5)3)2]PF6, which has been characterized by 1H, 2H, 19F and 31P NMR spectroscopy. Its structure has also been determined by a single crystal X-ray analysis. The crystal are monoclinic, space group P21/n, with cell dimensions a 20.012(5), b 17.222(5), c 8.902(3) Å and β 91.54(5)°. The structure was refined by full matrix least-squares methods on F, using 3097 unique observations collected by automated four circle diffractometer. Refinement converged at R 0.066. The Pt atom has a distorted square-planar coordination geometry, with cis P atoms, and PtP distances of 2.219(4) Å (trans to O) and 2.324(4) Å (trans to C). These results show the ethereal group is a weak ligand to platinum(II) but because of the chelating effect, its displacement by other ligands is thermodynamically not favorable. The mechanism of formation of the ethereal complex is also discussed. 相似文献
6.
Reaction of potassium dichromate with gamma-glutamylcysteine, N-acetylcysteine, and cysteine in aqueous solution resulted in the formation of 1:1 complexes of Cr(VI) with the cysteinyl thiolate ligand. The brownish red Cr(VI)-amino acid/peptide complexes exhibited differential stability in aqueous solutions at 4 degrees C and ionic strength = 1.5 M, decreasing in stability in the order: gamma-glutamylcysteine > N-acetylcysteine > cysteine. (1)H, (13)C, and (17)O NMR studies showed that the amino acids act as monodentate ligands and bind to Cr(VI) through the cysteinyl thiolate group, forming RS-Cr(VI)O(3)(-) complexes. No evidence was obtained for involvement of any other possible ligating groups, e.g., amine or carboxylate, of the amino acid/peptide in binding to Cr(VI). EPR studies showed that chromium(V) species at g = 1.973-4 were formed upon reaction of potassium dichromate with gamma-glutamylcysteine and N-acetylcysteine. Reaction of potassium dichromate or sodium dichromate with N-acetylcysteine and the methyl ester of N-acetylcysteine in N,N-dimethylformamide (DMF) also led to the formation of RS-Cr(VI)O(3)(-) complexes as determined by UV/vis, IR, and (1)H NMR spectroscopy. Thus, an early step in the reaction of Cr(VI) with cysteine and cysteine derviatives in aqueous and DMF solutions involves the formation of RS-CrO(3)(-) complexes. The Cr(VI)-thiolate complexes are more stable in DMF than in aqueous solution, and their stability towards reduction in aqueous solution follows the order cysteine < N-acetylcysteine < gamma-glutamylcysteine < glutathione. 相似文献
7.
Reed M. Izatt Robert M. Haws John D. Lamb David V. Dearden Philip R. Brown Don W. McBride Jr. James J. Christensen 《Journal of membrane science》1984,20(3):273-284
Cation fluxes were determined for various three-component, equimolar mixtures of alkali metal, alkaline earth, and Pb2+ cations in a H2O---CHCl3---H2O liquid membrane system incorporating macrocyclic polyethers as carriers. Carrier ligands studied were 18-crown-6, dicyclohexano-18-crown-6, 1,10-diaza-18-crown-6, 21-crown-7, dibenzo-24-crown-8, and cryptand [2.2.2]. Correlations were found between transport and relative cation:polyether cavity radii, the type of substituents present on the polyether ring, and the type and number of donor atoms present. All the ligands studied transported Pb2+ at higher rates than the other Mn+ in the mixtures. Transport behavior in these multi-cation systems can be predicted from Mn+—polyether complex stability constant data in most cases. 相似文献
8.
Jennifer T. Duong Mark J. Bailey Teresa E. Pick Patrick M. McBride Evelyn L. Rosen Raffaella Buonsanti Delia J. Milliron Brett A. Helms 《Journal of polymer science. Part A, Polymer chemistry》2012,50(18):3719-3727
Water‐dispersible, polymer‐wrapped nanocrystals are highly sought after for use in biology and chemistry, from nanomedicine to catalysis. The hydrophobicity of their native ligand shell, however, is a significant barrier to their aqueous transfer as single particles. Ligand exchange with hydrophilic small molecules or, alternatively, wrapping over native ligands with amphiphilic polymers is widely employed for aqueous transfer; however, purification can be quite cumbersome. We report here a general two‐step method whereby reactive stripping of native ligands is first carried out using trialkyloxonium salts to reveal a bare nanocrystal surface. This is followed by chemically directed immobilization of a hydrophilic polymer coating. Polyacrylic acids, with side‐chain grafts or functional end groups, were found to be extremely versatile in this regard. The resulting polymer‐wrapped nanocrystal dispersions retained much of the compact size of their bare nanocrystal precursors, highlighting the unique role of monomer side‐chain functionality to serve as effective, conformal ligation motifs. As such, they are well poised for applications where tailored chemical functionality at the nanocrystal's periphery or improved access to their surfaces is desirable. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
9.
We study the index problem for the d-bar operators subject to Atiyah- Patodi-Singer boundary conditions on noncommutative
disk and annulus. 相似文献
10.
Richard D. McBride 《Mathematical Programming》1980,18(1):49-61
A dynamic factorization algorithm is developed which algebraically partitions the basis inverse in such a manner so that the simplex method can be executed from a series of small inverses and the basis itself. This partition is maintained dynamically so that the additional memory required to represent the basis inverse reduces to this series of small inverses for in-core implementations.The algorithm is intended for use in solving general large-scale linear programming problems. This new method of basis representation should permit rather large problems to be solved completely in-core.Preliminary computational experience is presented and comparisons are made with Reid's sparsity-exploiting variant of the Bartels—Golub decomposition for linear programming bases. The computational experience indicated that a significant reduction in memory requirements can usually be obtained using the dynamic factorization approach with only a slight (up to about 20%) degradation of execution time.This research was supported in part by the Air Force Office of Scientific Research, Air Force System Command, USAF, under AFOSR Contract/Grant Number AFOSR-74-2715. 相似文献