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11.
Benito Alcaide Rafael Prez-Ossosio Joaquin Plumet Miguel A. Sierra 《Tetrahedron letters》1982,23(52):5585-5586
The monoimine easily formed bydirect condensation between benzil and 2-aminopyridine adds alcohols and amines to the imine bond without catalysis. A concerted mechanism is proposed. 相似文献
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Cyclic beta-keto ester monoanions react with 1,4-dihalobutenes to give C-alkylated products which subsequently undergo a stereoselective SN2' O-alkylation reaction to yield functionalized enol ethers. When the starting material was ethyl cyclopentanone carboxylate, the C-alkylated product, treated with a base, directly afforded the functionalized bicyclo[4.2.1]nonanone. The enol ethers were submitted to a flash vacuum thermolysis (FVT) reaction to readily afford functionalized bicyclo[4.n.1]alkanones (n = 3, 4). This reaction sequence was applied to the synthesis of a functionalized tricyclo[7.4.1.0(1,5)]tetradecanone, which represents an analogue to the tricyclic core of ingenol. 相似文献
14.
David Jacob Joaquin Fernández-Rossier 《The European Physical Journal B - Condensed Matter and Complex Systems》2016,89(10):210
Quantum spin tunneling and Kondo effect are two very different quantum phenomena that produce the same effect on quantized spins, namely, the quenching of their magnetization. However, the nature of this quenching is very different so that quantum spin tunneling and Kondo effect compete with each other. Importantly, both quantum spin tunneling and Kondo effect produce very characteristic features in the spectral function that can be measured by means of single spin scanning tunneling spectroscopy and allows to probe the crossover from one regime to the other. We model this crossover, and the resulting changes in transport, using a non-perturbative treatment of a generalized Anderson model including magnetic anisotropy that leads to quantum spin tunneling. We predict that, at zero magnetic field, integer spins can feature a split-Kondo peak driven by quantum spin tunneling. 相似文献
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16.
Isac-García J Hernández-Mateo F Calvo-Flores FG Santoyo-González F 《The Journal of organic chemistry》2004,69(1):202-205
The reactivity of 2-deoxy-2-iodoglycosyl isothiocyanates toward O- and S-nucleophiles gives an easy access to 2-deoxy-2-iodoglycopyranosyl thiocarbamates and dithiocarbamates. Internal nucleophilic displacement of the iodine by the sulfur atom in these compounds allows the preparation of glycopyranoso[1,2-d]-1,3-thiazoles and glycopyranoso[1,2-d]-1,3-thiazolidin-2-one or -2-thione. Reaction with amines or polyamines as N-nucleophiles led directly to 2-aminoglycopyranoso[1,2-d]-1,3-thiazoles without isolation of the intermediate thioureas. Methyl 2-deoxy-2-iodoglycopyranosyl thiocarbamates also allow the synthesis of 2-deoxyglycopyranosyl thiocarbamates or 2-deoxy-2-iodoglycopyranosyl carbamates. 相似文献
17.
Here, we show that Au nanoparticles having diameters of less than 2.2 nm can be extracted from within the interior of PAMAM dendrimers using n-alkanethiol extractants. Extraction proceeds quickly, regardless of the size of the nanoparticle, the dendrimer generation, or the peripheral functionalization of the dendrimer. The extraction rate is fastest for the lowest generation dendrimers, the smallest nanoparticles, and the shortest chain-length n-alkanethiols. Other important results of this study include the following. First, within the accuracy of absorbance spectroscopy, the extraction yield is quantitative. Second, NMR and FT-IR spectroscopy indicate that after extraction the dendrimer remains in the aqueous phase and can be used to template additional metal particles. Third, the size and optical characteristics of the extracted nanoparticles are the same as the precursor dendrimer-encapsulated nanoparticles (DENs). Fourth, a 100-fold excess of n-alkanethiol molecules is required to prevent aggregation of DENs during extraction. 相似文献
18.
Thermogravimetric study of the pyrolysis of waste wood 总被引:6,自引:0,他引:6
A thermogravimetric study of the pyrolysis of three different types of waste wood (forest wood, old furniture and used pallets) is carried out in a TGA equipment using dynamic and isothermal techniques. Isothermal runs were carried out at two temperature levels, one between 225° and 325°C (low range) and the other, between 700° and 900°C (high range). Results show a good agreement between the kinetic parameters obtained from either dynamic or isothermal techniques. It must be remarked that the own chemical composition of each type of wood together with the compounds added to the wood for each application, play a fundamental role in the kinetic behavior of their thermal decomposition. 相似文献
19.
Regioselective Synthesis of Polyheterohalogenated Naphthalenes via the Benzannulation of Haloalkynes 下载免费PDF全文
Dr. Dan Lehnherr Joaquin M. Alzola Dr. Emil B. Lobkovsky Prof. Dr. William R. Dichtel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(50):18122-18127
Independent control of halide substitution at six of the seven naphthalene positions of 2‐arylnaphthalenes is achieved through the regioselective benzannulation of chloro‐, bromo‐, and iodoalkynes. The modularity of this approach is demonstrated through the preparation of 44 polyheterohalogenated naphthalene products, most of which are difficult to access through known naphthalene syntheses. The outstanding regioselectivity of the reaction is both predictable and proven unambiguously by single‐crystal X‐ray diffraction for many examples. This synthetic method enables the rapid preparation of complex aromatic systems poised for further derivatization using established cross‐coupling methods. The power and versatility of this approach makes substituted naphthalenes highly attractive building blocks for new organic materials and diversity‐oriented synthesis. 相似文献
20.
Ceren Kütahyali Joaquin Cobos Vincenzo V. Rondinella 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(1):1-5
Results from tests aimed at optimizing an instrumental procedure for the direct and fast determination of uranium in solution
by laser fluorescence are presented. A comparison of sample fluorescence measured using different fluorescence enhancing reagents
was performed: sodium pyrophosphate, orthophosphoric acid, sulphuric acid and a commercially available fluorescence enhancer
were tested for the determination of uranium. From the experimental results, 0.01 M Na4P2O7·10H2O showed the best performance. Effects of reagent pH, different matrices, different concentrations of dissolved Th, and sample
volume were investigated. Applications of the improved procedure for the determination of uranium in samples arising from
UO2-based high level nuclear waste dissolution studies are described. 相似文献