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21.
22.
Xiaoxia WangYongmin Zhang 《Tetrahedron》2003,59(23):4201-4207
N-Acylbenzotriazoles, when treated with samarium diiodide in THF, undergo self-coupling reaction to afford 1,2-diketones in good to excellent yields; while when treated with samarium diiodide in CH3CN, they undergo ring-opening reaction to afford 1-acylamido-2-alkyl (or aryl) benzimidazoles in reasonable to good yields. A plausible mechanism was suggested. 相似文献
23.
A new series of group 6 carbonyl complexes of N-[(2-pyridyl)methyliden]-α (or β)-aminonaphthalene (α/β-NaiPy) are described in this work. The complexes are formulated as cis-[M(CO)4(α/β-NaiPy)] by elemental, mass and other spectroscopic data. The complexes show emission spectra at room temperature and their quantum yield lies between 0.4 and 0.5. All the complexes exhibit negative solvatochromism. Cyclic voltammetry shows metal centred oxidation and ligand reductions. 相似文献
24.
V. V. Nikitenko A. I. Martynenko S. A. Ostrovsky V. V. Rusak V. V. Kryuchkov D. A. Topchiev 《Russian Chemical Bulletin》1993,42(2):378-380
3-Methyl-l-vinylpyrazole (M3VP) and 5-methyl-1-vinylpyrazole (M5VP) were isolated as individual substances by vacuum rectification of their mixture (M3VP: M5VP 60 40). For each of them the kinetics of free-radical polymerization in MeOH were measured at low conversions. In both cases the rate of polymerization is proportional to 0.5 order with respect to the initiator (AIBN) concentration. On the other hand, a first order of reaction with respect to monomer concentration is observed only when the latter is relatively low (3M). At higher initial concentrations of monomers the order of reaction becomes less than unity. The overall rate of polymerization for M5VP was higher than for M3VP, whereas the initiation rate remained constant in the whole range of monomer concentrations and did not depend on the exact structure of the monomer. The difference in the rates of polymerization observed for M3VP and M5VP is probably connected with the difference in the key parameterk
p/k
t
1/2
for each of the two isomers. It is concluded that the correct kinetic information about homo- and co-polymerization of M3VP and M5VP cannot be obtained without their adequate separation.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 413–415, February, 1993. 相似文献
25.
This paper describes some thermal analysis experiments conducted on high explosive samples. These employ differential scanning calorimetry to monitor thermal effects at elevated temperatures (around 200 °C) and heat conduction calorimetry to record thermal effects at much lower temperatures (below 100 °C).The work shows that, due to the generally high thermal stability of many high explosive compositions, heat generation rates are very low, if detectable at all, at normal storage temperatures, even when using a very sensitive instrument. The sensitivity and reproducibility of this technique has been investigated in detail by Wilker et al. [S. Wilker, U. Ticmanis, G. Pantel, Detailed investigation of sensitivity and reproducibility of heat flow calorimetry, in: Proceedings of the 11th Symposium on Chemical Problems Connected with the Stability of Explosives, Sweden, 1998] and shown to be capable of recording heat generation rates of less than a microwatt. This allows continuous measurement of decomposition processes in nitrate ester based propellants at temperatures as low as 40 °C. However, the measurement of very low levels of heat generation is difficult, time consuming and therefore expensive. If the assumption is made that the life limiting process is invariably the slow decomposition of the energetic component, this will frequently lead to very long service lifetime predictions.A number of possible complications are identified. Firstly, due to its low detection threshold, a heat conduction calorimeter may detect other reactions which will not lead to failure, but which may still dominate the heat flow signal. Secondly, the true failure process may generate little energy and be overlooked. In view of these considerations, at present it seems unwise to rely on heat conduction microcalorimetry as the only tool for the assessment of the life of high explosive energetic systems.Based on examples of life terminating processes in high explosives during storage and use, it is clear that decomposition of the energetic material is not invariably the cause of system failure. It is also by no means the only reaction that may take place in, and be observed by, a heat conduction calorimeter. 相似文献
26.
Heterobimetallic alkoxides are broadly recognized as versatile precursors for luminescence materials, and efforts are being made to develop novel routes by applying the concept of geometrical molecular design, for their synthesis and to design a single source precursor suited to photoluminescent materials. Novel and new series of bimetallic alkoxides has been prepared by metathesis route. They exhibit a lower sensitivity towards hydrolysis and so they are easier to handle as compared to other alkoxides. All the compounds were characterized by elemental analysis, FT-IR and multinuclear NMR spectroscopies. FT-IR revealed that the molecular structure of these metal alkoxides was retained to a large extent in 4 : 1 halogenated alcohol-benzene solution. The heteronuclear NMR spectroscopy provided useful information about chemical shifts for better understanding the likely structure based on interactions with their coordinate metals. The mass spectra show similar types of fragmentation pattern. SEM-EDS analyses showed consistency with the formulation. XRD patterns show an enhanced homogeneity at high temperature. TGA measurements show that thermal decomposition occured in steps that depended entirely on the chemical compositions and the synthesis routes. SEM observation reveals that the morphology and particle size strongly depend on synthesis routes for their precursors. 相似文献
27.
Marjan Kočevar Bojan Verček Branko Stanovnik Miha Tišler 《Monatshefte für Chemie / Chemical Monthly》1982,113(6-7):731-744
Pyrazine- and pyridinecarboxamidoximes with an amino, potentially tautomeric hydroxy or mercapto group inortho position could be transformed in the appropriate condensed azines. In this manner, representatives of pyrazolo(3,4-b)pyrazine, isoxazolo(4,5-b)pyrazine and isothiazolo(5,4-b)pyridine ring system were synthesized and some transformations investigated.Presented in part at the 8th International Congress of Heterocyclic Chemistry, Graz, 1981. 相似文献
28.
V. I. Dimitrov J. D'Haan G. Knuyt C. Quasyhaegens L. M. Stals 《Applied Physics A: Materials Science & Processing》1996,63(5):475-480
A diffusion model of metal surface modification by plasma nitriding has been developed. This model takes into account the erosion effects at the plasma/solid interface occurring due to the ion bombardment of the surface. For constant sputtering rate, which is the usual situation during plasma nitriding, the growth of the sub-layers is well described by the analytical expressiong(t) =g
0,f
–1 (t/t
0), whereg(t) is the sub-layer thickness at timet,g
0 andt
0 are parameters which depend on the treated material and plasma characteristics,f
–1 is the inverse of the function — In(1 - x) + x), 0 x 1. Under negligible erosion effects, the expression forg(t) reduces to the parabolic law. The diffusion zone (substratum) growth does not follow the parabolic law as well. However, the deviation occurs after long plasma nitriding time. The model can be used for experimentally determining the effective diffusion coefficients and the erosion rate during plasma nitriding of metal surfaces. 相似文献
29.
IR lattice vibration spectra were used to monitor the changes in the structure of zeolite Na-Y upon its dealumination with ethylenediaminetetraacetic acid (EDTA) or with HCl. The terminal Si-O(H,Na) bonds thus formed (which are detectable by characteristic absorbance at v 900–950 cm–1) are energetically less uniform when EDTA has been used as the dealuminating agent. This inhomogeneity is connected with the local deformations of zeolite structure which result in lowering the symmetry of silicon-oxygen tetrahedra. As a consequence, two novel bands appear at v 1090 cm–1 and 1200 cm–1 in addition to the fundamental absorption bands, vas (TO4) (T = Si, Al), at 1030 cm–1 and 1145 cm–1. A mechanism of dealumination is proposed, which takes into account the topochemical peculiarities involved in the chelation of the framework aluminum ions with EDTA.Translated fromIzyestiya Akademii Nauk. Seriya Khimicheskay, No. 2, pp. 284–287, February, 1993. 相似文献
30.