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181.
Pedro MaroteBernard Durand Jean-Pierre Deloume 《Journal of solid state chemistry》2002,163(1):202-209
Zirconia powders are prepared by reaction of a zirconium precursor with an alkali metal nitrate. The major part of the reactions takes place before the melting points and then the reactions go slowly to completion at 450°C in the molten salts. The roles of the precursor and the alkali metal ion are discussed considering the reaction between two precursors, octahydrated zirconium oxychloride and zirconium tetrachloride, and two nitrates, LiNO3 and NaNO3, and some resulting physico-chemical differences. The obtained zirconia powders contain very small amounts of alkali metal ions which act as stabilizing agent. Their effect on the balance tetragonal-monoclinic ZrO2 depends upon the homogeneity of their distribution which is related to their ability to diffuse inside the bulk of particles and their polarizing power when located mainly on the surface. 相似文献
182.
Morilla ME Morfes G Nicasio MC Belderrain TR Mar Díaz-Requejo M Graiff C Tiripicchio A Sánchez-Delgado R Pérez PJ 《Chemical communications (Cambridge, England)》2002,(17):1848-1849
N,N, N',N'-Tetraethylethylenediamine undergoes simple or double intramolecular dealkylation reactions in the presence of the complexes [RuCl2(diene)]n (diene = cod, nbd) or trans-[RuCl2(diene)(morfoline)2 at 80 degrees C to afford chelating amine ligands which contains one or two N-H functionalities. 相似文献
183.
Díaz-Requejo MM Caballero A Belderraín TR Nicasio MC Trofimenko S Pérez PJ 《Journal of the American Chemical Society》2002,124(6):978-983
In situ prepared copper catalysts Tp(X)Cu (Tp(X) = homoscorpionate) catalyze the olefin cyclopropanation reaction using ethyl diazoacetate as the carbene source. Very high values of both activity and diastereoselectivity toward the cis isomer have been obtained for styrene, alpha-methylstyrene, 1-hexene, 1-octene, vinyl acetate, n-butyl vinyl ether, 2,5-dimethyl-2,4-hexadiene, and 3,3-dimethyl-1-butene. The effect of the temperature in the diastereoselectivity was almost negligible within the range -10 to +30 degrees C. Kinetic studies have allowed us to propose that the homoscorpionate ligand might act in a dihapto form during the catalytic process. This transformation seems to operate under kinetic control, where the formation of the cis isomer would govern the reaction rate. 相似文献
184.
Díaz-Requejo MM Belderraín TR Nicasio MC Trofimenko S Pérez PJ 《Journal of the American Chemical Society》2002,124(6):896-897
A series of catalysts of general formula TpXCu (TpX = homoscorpionate ligand) promote the insertion of :CHCO2Et (ethyl diazoacetate as the carbene source) into the C-H bonds of cycloalkanes and cyclic ethers in moderate to high yield. A correlation between the steric hindrance of these catalysts and the yield of the transformation has been observed. 相似文献
185.
We present the results of an experimental study of patterned segregation in a horizontally shaken shallow layer of a binary mixture of dry particles. An order parameter for the segregated domains is defined and the effect of the variation of the combined filling fraction, C, of the mixture on the observed pattern formation is systematically studied. We find that there is a critical event associated with the onset of segregation, at C(c)=0.647+/-0.049, which has the characteristics of a continuous phase transition, including critical slowing down. 相似文献
186.
Juan?Antonio?MaestroEmail author Daniel?Mozos Raquel?Dormido Pedro?Reviriego 《Design Automation for Embedded Systems》2004,9(3):193-210
As Codesign problems become larger and more realistic, the required time to estimate their solutions turns into an important bottleneck. This paper presents a new approach to improve the traditional estimation techniques, in order to avoid this drawback. The presented method has been successfully tested on a large experimental benchmark, attaining quality levels close to those provided by the Synopsys Behavioral Compiler. Finally, a case study based on the standard H.261 video co-dec is described, proving the convenience of the technique on real-life situations. The obtained results show a significant improvement in the process time, while keeping the good precision and fidelity levels that the traditional estimation models usually offer. 相似文献
187.
Besada P Mamedova L Thomas CJ Costanzi S Jacobson KA 《Organic & biomolecular chemistry》2005,3(10):2016-2025
Diketopiperazines (DKPs) are a common motif in various biologically active natural products, and hence they may be useful scaffolds for the rational design of receptor probes and therapeutic agents. We constructed a new bicyclic scaffold that combines a DKP bridged with a 10-membered ring. In this way we obtained a three-dimensional molecular skeleton, with several amendable sites that provide a starting point to design a new combinatorial library having diverse substituent groups. Structural variation is based upon the flexibility of alkylation of the nitrogen atoms of the DKP and on the side-chain olefin. We obtained a 10-membered secondary ring through a ring-closure metathesis reaction using the second generation Grubbs catalyst. Rings containing both O-ethers and S-ethers were compared. N-Alkyl or arylalkyl groups were introduced optionally at the two Nalpha-atoms. This is a general scheme that will allow us to test rings of varying sizes, linkages, and stereochemical parameters. The DKP derivatives were tested for activity in astrocytoma cells expressing receptors coupled to phospholipase C. Inhibitory effects were observed for signaling elicited by activation of human nucleotide P2Y receptors but not m3 muscarinic receptors. Compound 20 selectively inhibited calcium mobilization (IC50 value of 486 +/- 16 nM) and phosphoinositide turnover elicited by a selective P2Y1 receptor agonist, but this compound did not compete for binding of a radiolabeled nucleotide-competitive receptor antagonist. Therefore, the new class of DKP derivatives shows utility as pharmacological tools for P2Y receptors. 相似文献
188.
Basurto S Torroba T Comes M Martínez-Máñez R Sancenón F Villaescusa L Amorós P 《Organic letters》2005,7(24):5469-5472
[structure: see text] A new sensory MCM-41-based material for the colorimetric sensing and discrimination of amines has been developed. 相似文献
189.
A new route for the degradation of the saturated side chain of dihydrozamoranic acid has been devised, giving an advanced intermediate, compound 14, useful for the synthesis of insect antifeedants such as warburganal and polygodial. 相似文献
190.
Fructos MR Belderrain TR Nicasio MC Nolan SP Kaur H Díaz-Requejo MM Pérez PJ 《Journal of the American Chemical Society》2004,126(35):10846-10847
The complex IPrCuCl (1) catalyzes the transfer of the :CHCO2Et group from ethyl diazoacetate (EDA) to unsaturated and saturated substrates (olefins, amine, alcohols) with very high yields. In the absence of substrate, the complex 1 does not react with EDA to give the diazo coupling products (fumarate and maleate), a rare example in the field of metal-catalyzed diazocompounds decomposition. 相似文献