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41.
Preparation of Ammonium Rare Earth Halides totally free of Water Ammonium rare earth halides totally free of traces of water were prepared in an one step synthesis from metal, ammonium halide, and halogen in a two step temperature regime. 相似文献
42.
综述了亚甲胺叶立德的制备、它参与的[3+2]环加成反应的反应机理、反应选择性及在天然产物全合成中的应用等方面的最新进展. 相似文献
43.
Farajollah?MohanazadehEmail author Mostafa?Hosini Mahmoud?Tajbakhsh 《Monatshefte für Chemie / Chemical Monthly》2005,136(12):2041-2043
Summary. Reduction of aldehydes and ketones to the corresponding alcohols was achieved in a simple procedure using the system sodium
borohydride and ammonium carbonate. This system needs lower excesses of reducing agent and leads to significantly shortened
reaction times. 相似文献
44.
Hiroshi Ito 《Tetrahedron letters》2005,46(50):8757-8760
Fourteen isomers of bis(formylmethano)C60 were isolated and characterized. A mixture of the bisadducts was obtained by the reaction of C60 with an α-formylsulfonium ylide, and then separated into 15 fractions by preparative HPLC, preparative TLC, and recycling preparative HPLC. Fourteen of the fifteen fractions were found to consist of a single isomer, respectively, which were assigned to the trans-2 (3 diastereo-isomers), trans-3 (3 diastereo-isomers), trans-4 (3 diastereo-isomers), equatorial (2 diastereo-isomers), and cis-2 (3 diastereo-isomers) bisadducts by the comparison of their UV/vis spectra with those of the bisadducts obtained by the Bingel-Hirsch reaction. The 1H and 13C NMR analysis, the transformation of the formyl groups, and the dipole moment calculation clarified the stereochemistry of the substituents on the two cyclopropane bridge-head carbons (in/in, in/out, and out/out). 相似文献
45.
A Setaram C-80 calorimeter has been modified in order to measure the heat flow of energetic materials at pressures up to 69 MPa. A manifold and sample cells capable of operating at high pressure were designed, constructed and evaluated. This paper will describe, in detail, the high pressure manifold construction, safety assessment and calibration. As well, the results for initial trials with ammonium nitrate (AN), and pentaerythritol tetranitrate (PETN) at various pressures and heating rates will be discussed. 相似文献
46.
Purification of plasmid DNA vectors by aqueous two-phase extraction and hydrophobic interaction chromatography 总被引:4,自引:0,他引:4
The current study explores the possibility of using a polyethyleneglycol(PEG)-ammonium sulphate aqueous two-phase system (ATPS) as an early step in a process for the purification of a model 6.1 kbp plasmid DNA (pDNA) vector. Neutralised alkaline lysates were fed directly to ATPS. Conditions were selected to direct pDNA towards the salt-rich bottom phase, so that this stream could be subsequently processed by hydrophobic interaction chromatography (HIC). Screening of the best conditions for ATPS extraction was performed using three PEG molecular weights (300, 400 and 600) and varying the tie-line length, phase volume ratio and lysate load. For a 20% (w/w) lysate load, the best results were obtained with PEG 600 using the shortest tie-line (38.16%, w/w). By further manipulating the system composition along this tie-line in order to obtain a top/bottom phase volume ratio of 9.3 (35%, w/w PEG 600, 6%, w/w NH4)2 SO4), it was possible to recover 100% of pDNA in the bottom phase with a three-fold increase in concentration. Further increase in the lysate load up to 40% (w/w) with this system resulted in a eight-fold increase in pDNA concentration, but with a yield loss of 15%. The ATPS extraction was integrated with HIC and the overall process compared with a previously defined process that uses sequential precipitations with iso-propanol and ammonium sulphate prior to HIC. Although the final yield is lower in the ATPS-based process the purity grade of the final pDNA product is higher. This shows that it is possible to substitute the time-consuming two-step precipitation procedure by a simple ATPS extraction. 相似文献
47.
O. V. Shishkin 《Russian Chemical Bulletin》1996,45(8):1833-1835
Molecular and electronic structures of 1,2-dihydropyridine, 1,2- and 1,6-dihydropyrimidine, and their oxo, imino, and methylene derivatives were studied by the semiempirical quantum-chemical AM1 method. In all compounds, the heterocycle exhibits a high conformational flexibility. The transition from a planar equilibrium conformation to a distorted sofa conformation with the =C-NH-C-C(N)= torsion angle of ±20° causes an increase in the energy by less than 1.7 kcal mol–1. All molecules have similar -electronic structures, which, apparently, determines the similarity in their conformational behavior. The bending strain and the nonaromatic character of the cyclic -system are the factors that stabilize the nonplanar conformation of the ring in unsubstituted dihydroazines and ylide derivatives, respectively.Translated fromIzvestiva Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1934–1937, August, 1996. 相似文献
48.
Chenmou Zheng Xinmin Zhang Shan He Qun Fu Deming Lei 《Journal of solid state chemistry》2003,170(2):221-226
V2O3 nanopowder with spherical particles was prepared by reducing pyrolysis of the precursor, (NH4)5[(VO)6(CO3)4(OH)9]·10H2O, in H2 atmosphere. The thermolysis process of the precursor in a H2 flow was investigated by thermogravimetric analysis and differential thermal analysis. The results indicate that pure V2O3 forms at 620°C and crystallizes at 730°C. The effects of various reductive pyrolysis conditions on compositions of V2O3 products were studied. Scanning electron micrographs show that the particles of the V2O3 powder obtained at 650°C for 1 h are spherical about 30 nm in size with more homogeneous distribution. Experiments show that nanopowder has larger adsorption capacity to gases and is more easily reoxidized by air at room temperature than micropowder. Differential scanning calorimetry experiment indicates that the temperature of phase transition of nano-V2O3 powder is −119.5°C on cooling or −99.2°C on heating. The transition heats are −12.55 J g−1 on cooling and 11.42 J g−1 on heating, respectively. 相似文献
49.
Sylvain Celanire Frederic Marlin Jack E. Baldwin Robert M. Adlington 《Tetrahedron》2005,61(12):3025-3032
The synthesis of 3,11-dioxatricyclo[5.3.1.01,5]undeca-5,9-dien-8-ones is reported from suitable 5-substituted furfuryl alcohols bearing an acetylenic side-chain. Successive peracid-mediated oxidative rearrangement of furan carbinols and base-assisted intramolecular 1,3-dipolar cycloaddition afforded oxygen-bridged tricyclo-undecane derivatives. Stereoselective transformations of cycloadducts are also discussed. 相似文献
50.
The reaction of electron-deficient cyclopropane derivatives, cis-1-methoxycarbonyl-2-aryl-6,6-dimethyl-5,7dioxospiro[2,5]octa-4,8-diones with benzoylmethylenetriphenylarsorane (2) and methoxycarbonylmethylenetriphenylarsorane (4) was found to form cis,trans-l-methoxycarbonyl-2-aryl-3-benzoyl-7,7-dimethyl-6,8-dioxospiro[3,5]nona-5,9-dione (3a-3e) and trans,cis,trans-5-[2‘-methoxycarbonyl-2‘-(triphenylarsoranylidene)acetyl]-6oxo-3-aryl-tetrahydro-pyran-2,4-dicarboxylic acid dimethyl esters (5a-5c) respectively with high stereoselectivity. The possible reaction mechanisms for the formation of the different products were also orooosed. 相似文献