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1.
Flávia Manarin 《Tetrahedron letters》2007,48(28):4805-4808
We present here a simple and mild method of hydrothiolation of internal and terminal alkynes under PhSeBr-catalyzed reaction in the absence of solvent at room temperature. The reaction tolerates a wide variety of substituents on thiol, and provides the corresponding product in good yield and selectivity. 相似文献
2.
The total synthesis of 1-(Z)-atractylodinol, a natural polyacetylenic alcohol with several biological activities, has been achieved using a newly developed telluride synthon and a novel use for the Negishi type coupling reaction employing vinyl tellurides. 相似文献
3.
O. N. Litvinenko A. N. Kuznetsov A. V. Olenev B. A. Popovkin 《Russian Chemical Bulletin》2007,56(10):1945-1947
Three new mixed tellurides of nickel and group 13–14 metals Ni3−δMTe2 (M = Sn, In, Ga) were prepared by high-temperature ampoule synthesis and studied by powder X-ray diffraction analysis. The
compound Ni3−δSnTe2 was also studied by single crystal X-ray diffraction analysis. The structural model of this phase and two analogs was described
as consisting of layers with nickel-main group metal bonds confined from the above by tellurium atoms. The van der Waals gap
formed through contacts between the tellurium atoms of neighboring layers is partially occupied by nickel atoms.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1879–1881, October, 2007. 相似文献
4.
The reactivity of a Cr‐Te multilayer film consisting of 326 Cr/Te double‐layers with about 88(3) at% Te was investigated with in‐situ X‐ray diffraction. The occurrence of a superstructure reflection caused by the multilayer system is observed. During the annealing procedure between 80 and 90 °C the layer‐by‐layer arrangement is destroyed and elemental Te crystallizes. After 6 h isothermal annealing at 140 °C CrTe3 starts to crystallize. The amount and the crystal size of CrTe3 increase with raising temperature and Te is consumed during the growth process. At 220 °C the formation of crystalline Cr2Te3 is observed and between 220 and 260 °C CrTe3 is completely decomposed into Cr2Te3. The two Cr tellurides grow as highly textured materials. The size of CrTe3 crystals is significantly larger than that of Cr2Te3. For a co‐deposited Cr‐Te film with composition 77(3) at% Te the tri‐telluride and elemental Te crystallize simultaneously. The texture of CrTe3 is less pronounced and different reflections of the tri‐telluride occur besides the (h00)‐reflections. Up to 160 °C a pronounced increase of the crystallite size is observed and the crystals are significantly larger than those obtained with the multifilm sample. At 130 °C the crystallization kinetics seem to be controlled by nucleation. 相似文献
5.
The Negishi cross-coupling reaction of vinylic- and aryltellurides with heteroarylzinc chlorides catalyzed by PdCl2/CuI is described. This cross-coupling reaction is general and permits the formation of a new sp2-sp2 carbon bond in good yields and high stereoselectivity. 相似文献
6.
Vinyl- and 1-alkenyldichloroboranes were used as dienophiles for the Diels–Alder reaction with representative aliphatic and cyclic 1,3-dienes. The organoborane adducts were transformed into the corresponding olefins either by protonolysis or by oxidation–mesylation–reduction. Direct protonolysis of the adducts gave in most cases mixtures of olefins whereas the reduction of mesylates with lithium triethylborohydride produced pure olefins in good yields. 相似文献
7.
《Journal of Dispersion Science and Technology》2013,34(2-3):231-244
Several monomers (i.e., acrylonitrile (ACN), ethyl acrylate (EtA), acrylate of 2 ethylhexyl (EHA), butyl acrylate (BuA), vinyl acetate (VAc), methyl methacrylate (MMA) and styrene (St)) were investigated in order to study their capacities to form microemulsions. The surfactant was nonyl phenol ethoxylate with 25 moles ethylene oxide and ethanol was used as the cosurfactant. The phase diagrams prove that the capacity for microemulsion formation varies in the following sequence: ACN = EtA > VAc > BuA > MMA > St > EHA. Conductometric and refractometric studies allowed us to evidence the formation of microemulsions with W/O, bicontinuous or O/W structure. Fluorescence studies give interesting informations on the stabilization capacity of the monomers dispersed by interaction with hydrophobic chain of the cosurfactant. H-NMR studies suggest that the monomers in microemulsions lie in regions with various polarities as function of their chemical nature. In polymerization initiated with benzoyl peroxide the minimum conversions were obtained in zones of composition where the initial microemulsions possess a bicontinuous microstructure. The reactions of degradative transfer of the increasing macroradicals account for these conversion modifications. For initiation with ammonium persulphate, its rate of decomposition depends on its ability to displace the proton bonded to the substituted vinylic carbon of the monomer. The productivity of this initiator varies within the sequence MMA > EtA > BuA > St > ACN > VAc. The consumption of the initiator, as induced by the monomer, depends on its chemical nature and on the solubilization site of the microemulsions. 相似文献
8.
The lattice dynamics in as‐cast and nanocrystalline thermoelectric Bi2Te3 based p‐type and n‐type material were investigated using inelastic neutron scattering. Generalized densities of phonon states show substantial agreement between the lattice dynamics in as‐cast samples and previous studies. The lattice dynamics in the nanocrystalline materials differ significantly from its as‐cast counterparts in the acoustic phonon regime. In nanocrystalline p‐type and n‐type compounds, the average acoustic phonon group velocity was found to be reduced to 80(5)% and 95(2)% of the value in as‐cast material. It is argued that point‐defect and strain contrast scattering may play an important role for the understanding of lattice thermal conductivity in (nanocrystalline) Bi2Te3 based thermoelectrics beside the observed decrease of sound velocity. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim) 相似文献
9.
Claudio C. Silveira Paulo Cesar S. Santos Samuel R. Mendes Antonio L. Braga 《Journal of organometallic chemistry》2008,693(26):3787-3790
A general method for the synthesis of vinylic chalcogenides by nucleophilic and Ni-catalyzed vinylic substitution on vinylic halides by phenyl chalcogenolates is described. The reactions were regio and stereoselective for the nickel catalyzed substitution, and mixture of isomers was observed for some examples in the thermal process in DMF. 相似文献
10.
Thioether 4‐[(1′E,3′E)‐4′‐phenylsulfanyl‐1,3′‐butadienyl]pyridine 8 and sulfone 4‐(4′‐phenylsulfonyl‐1′,3′‐butadienyl)pyridine 14 were prepared by reaction of the carbanions derived from allylic thioether or allylic sulfone with isonicotinaldehyde. The reaction with the sulfonyl carbanion occurred at the α position and on heating the alcolate gave the dienic sulfone 14 . The corresponding pyridinium iodide 10 and 15 were prepared by reaction with methyl iodide, respectively, on pyridine derivates 8 and 14 . The dienic pyridinium thioether 10 showed a long wavelength absorption band centered at 420 nm. The reaction of dienic pyridinium sulfone 15 with thiophenol gave the dienic pyridinium thioether 10 by a nucleophilic vinylic substitution. The reaction of sulfone 15 with glutathione was of second order and the rate constant was 8.5 M?1s?1 at 30°C and pH 7, about 500 times smaller than the rate constant observed with (E)‐1‐methyl‐4‐(2‐methylsulfonyl‐1‐ethenyl)pyridinium iodide 1 . The dienic pyridinium thioether 10 was a negative solvatochrome. 相似文献