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41.
Rate constants for quenching of 1O2 by a number of strained molecules have been determined by the competitive rubrene photooxidation method; the rate constant for quenching by Q may be evaluated by adaption of a kinetic analysis already in the literature for the rubrene photooxidation method. 相似文献
42.
Potyrailo RA Chisholm BJ Morris WG Cawse JN Flanagan WP Hassib L Molaison CA Ezbiansky K Medford G Reitz H 《Journal of combinatorial chemistry》2003,5(4):472-478
Coupling of combinatorial chemistry methods with high-throughput (HT) performance testing and measurements of resulting properties has provided a powerful set of tools for the 10-fold accelerated discovery of new high-performance coating materials for automotive applications. Our approach replaces labor-intensive steps with automated systems for evaluation of adhesion of 8 x 6 arrays of coating elements that are discretely deposited on a single 9 x 12 cm plastic substrate. Performance of coatings is evaluated with respect to their resistance to adhesion loss, because this parameter is one of the primary considerations in end-use automotive applications. Our HT adhesion evaluation provides previously unavailable capabilities of high speed and reproducibility of testing by using a robotic automation, an expanded range of types of tested coatings by using the coating tagging strategy, and an improved quantitation by using high signal-to-noise automatic imaging. Upon testing, the coatings undergo changes that are impossible to quantitatively predict using existing knowledge. Using our HT methodology, we have developed several coatings leads. These HT screening results for the best coating compositions have been validated on the traditional scales of coating formulation and adhesion loss testing. These validation results have confirmed the superb performance of combinatorially developed coatings over conventional coatings on the traditional scale. 相似文献
43.
Karin Krüger Natalia V. Shakhlevich Yuri N. Sotskov Frank Werner 《The Journal of the Operational Research Society》1995,46(12):1481-1497
We consider a scheduling problem where a set of n jobs has to be processed on a set of m machines and arbitrary precedence constraints between operations are given. Moreover, for any two operations i and j values a ij >0 and a ji >0 may be given where a ij is the minimal difference between the starting times of operations i and j when operation i is processed first. Often, the objective is to minimize the makespan but we consider also arbitrary regular criteria. Even the special cases of the classical job shop problem J//Cmax belong to the set of NP-hard problems. Therefore, approximation or heuristic algorithms are necessary to handle large-dimension problems. Based on the mixed graph model we give a heuristic decomposition algorithm for such a problem, i.e. the initial problem is partitioned into subproblems that can be solved exactly or approximately with a small error bound. These subproblems are obtained by a relaxation of a subset of the set of undirected edges of the mixed graph. The subproblems are successively solved and a proportion of the results obtained for one subproblem is kept for further subproblem definitions. Numerical results of the algorithm presented here are given. 相似文献
44.
T. C. Awes C. Barlag F. Berger M. A. Bloomer C. Blume D. Bock R. Bock E. -M. Bohne D. Bucher A. Claussen G. Clewing L. Dragon A. Eklund S. Garpman R. Glasow H. Gustafsson H. H. Gutbrod G. Hölker J. Idh P. Jacobs K. H. Kampert B. W. Kolb H. Löhner I. Lund F. E. Obenshain A. Oskarsson I. Otterlund T. Peitzmann F. Plasil A. M. Poskanzer M. Purschke B. Roters S. Saini R. Santo H. R. Schmidt S. P. Sørensen K. Steffens P. Steinhaeuser E. Stenlund D. Stüken G. R. Young 《Zeitschrift fur Physik C Particles and Fields》1995,65(2):207-213
Correlations between protons are studied in the target fragmentation region of reactions of protons and16O with C, Cu, Ag, Au and of32S with Al and Au at 200A GeV. The emitted protons were measured with the Plastic Ball detector in the WA80 experiment at the CERN SPS. The comparison of the correlation function with calculations, assuming a spherical, gaussian shaped source with a lifetime τ=0 fm/c, allows the extraction of radius parameters. The values are very close to those expected from the geometry of the target nuclei and increase with the target mass as αA Target 1/3 . Even in proton induced reactions the whole target nucleus is involved. The dependence of the radii on centrality, polar angleθ lab, and energy, and their relation to measured proton yields are presented. 相似文献
45.
46.
White DB Tippens WB Abegg R Baldisseri A Boudard A Briscoe W Fabbro B Garçon M Hermes EA Jacobs WW Kessler RS Lytkin L Mayer B Nefkens BM Niebuhr C Petrov AM Poitou J Saudinos J Tomasi-Gustafsson E van der Schaaf A van Oers WT Vigdor SE Wang M 《Physical review D: Particles and fields》1996,53(11):6658-6661
47.
Frank Seela Karin Mersmann Jane A. Grasby Michael J. Gait 《Helvetica chimica acta》1993,76(5):1809-1820
A 7-deazaadenosine ( = tubercidin; c7A; 1 ) building block for solid-phase oligoribonucleotide synthesis was prepared. The amino group of 1 was protected with the (dimethylamino)methylidene residue (→ 3 ), and the monomethoxytrityl group was introduced at OH? C(5′) (→ 4 ). Protection of OH? C(2′) was carried out by silylation, showing that use of the (i-Pr)3Si group resulted in high 2′-O-selectivity (→ 5b , 80%). Reaction of 5b with PCl3 afforded the phosphonate 7 which was used in solid-phase oligoribonucleotide synthesis. The autocatalytic hydrolysis of hammerhead ribozymes using pG-G-G-A-G-U-C-A-G-U-C-C-C-U-U-C-G-G-G-G-A-C-U-C-U-G-A-A-G-A-G-G-C-G-C as substrate strand (S) and modified G-C-G-C-C-G-A-A-A-C-U-C-C-C as enzyme strand (E) was studied. When c7A replaced A13 or A14, a small decrease of catalytic activity was observed, while modification in position A15 enhanced the autocatalytic hydrolysis. The results demonstrate, that the atom N(7) of adenosine in any of these positions is not crucial for ribozyme action. 相似文献
48.
Adi Wolfson Ivo F.J. Vankelecom Pierre A. Jacobs 《Journal of organometallic chemistry》2005,690(15):3558-3566
When ionic liquids (ILs) are employed as solvents for transition metal complex (TMC) catalyzed reductions, a second solvent can be added to increase the efficiency of the catalytic cycle and the solubility of the reactant in the IL phase. Two industrially relevant asymmetric hydrogenations, the enantioselective reductions of methyl 2-acetamidoacrylate with Rh-EtDuPHOS and methyl acetoacetate with Ru-BINAP, were performed in different catalytic systems including 1-butyl-3-methylimidazolium hexafluorophosphate/ tetrafluoroborate as ILs. Product separation and TMC recycling was performed by extracting the product from the reaction mixture. This can be accomplished by cooling the system, by adding an excess of the second solvent or by adding a third solvent. A high solubility of the second solvent in the IL catalytic phase favors the reaction activity, but can induce leaching of the IL and TMC. 相似文献
49.
Sousa Pedrares A Teng W Ruhlandt-Senge K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(9):2019-2024
Novel magnesium pyridine-2-thiolates were prepared by using alkane elimination chemistry. The resulting complexes display a metal coordination environment composed of sulfur/nitrogen bonding from the intramolecularly stabilized mercaptopyridine ligand, in addition to coordination by the oxygen centers from two THF donors. The compounds are well-suited model compounds for the magnesium centers in Photosystem I, in which magnesium, situated in the central chlorophyll ligand, is bound to sulfur from a nearby methionine residue. All compounds were characterized by (1)H, (13)C NMR, and IR spectroscopy, in addition to Xray crystallography. 相似文献
50.
The formation of tin compounds on the surface of hydroxyapatite, the main crystalline component of teeth, is discussed controversially. SnF2 is used as an anticaries agent in toothpaste preparations. Pure hydroxyapatite (HAP) is treated with extracts of commercially available toothpastes containing tin fluoride and analyzed by electron spectroscopy (ESCA). Survey spectra and depth profiles are recorded. The chemical shifts measured for the HAP samples are compared with those of standard tin compounds. It is concluded that on the surface of hydroxyapatite a mixture of two-valent fluoro-phosphato compounds is formed. SnO is not found in the mixture. 相似文献