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1.
1.  In NaA zeolite a homocharge is formed by charges deposited on the surface of the zeolite from the gas gap between the electrode and the specimen.
2.  The existence of thermoelectret effects has been found in the systems NaA-zeolite -air, NaA-helium, NaA-nitrogen, and NaA-oxygen.
3.  The thermoelectret effects are caused by both the accumulation of charges in the specimen and the adsorption of molecules in the electric field.
4.  A low mobility has been noted for adsorbed molecules in the electret state of the system.
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2.
1.  An efficient method of aziridine dimer synthesis is presented involving reaction of aziridine with esters of strong organic acids followed by alkaline hydrolysis of the resultant N-acyl derivatives.
2.  New N-acyl and carbamoyl derivatives of aziridine dimer and trimer were synthesized.
3.  Linear and branched isomers of aziridine tetramer and also diastereomers of 2-methylaziridine dimer were isolated and characterized.
4.  An efficient regiospecific synthesis of 2,2-dimethylaziridine dimer and trimer was developed.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2566–2575, November, 1988.  相似文献   

3.
1.  The dipole moments of the two kinds of C-O bonds in acetals and their analogs are not identical.
2.  In formal molecules and the dimethylketal of acetone the C-O-C-O -C chains have gauche-gauche conformation, with the methyl groups lying on different sides of the O-C-O plane.
3.  The dimethylketal of tetrachlorocyclopentadienone is represented by a mixture of trans-gauche and gauche-gauche conformers.
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4.
1.  The molecular-sieve properties of a number of synthetic and natural chabazites have been investigated.
2.  Characteristic differences have been revealed in the molecular-sieve properties, thermal stability, and x-ray characteristics between the two groups of the zeolites studied.
3.  A reversal of the molecular-sieve effect on passing from the calcium to the sodium-calcium forms of certain synthetic and natural chabazites has been observed.
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5.
1.  N-Ethyl and N-isopropyl-3-piperidones were synthesized and the stereochemistry of their reduction was studied.
2.  The dependenceof stereochemistryof a series of reactions at the carbonyl center on bulk of the substituent on nitrogen was established.
3.  Pure a- and e-epimers of N-ethyl- and N-isopropyl-3-piperidols were separated.
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6.
1.  The condensation of 1,2-hydroxylamino oximes with biacetyl leads to 1-hydroxy-2-acetyl-2,4,5,5-tetrasubstituted 3-imidazoline 3-oxides.
2.  When 1-hydroxy-2-acetyl-2,5,5-trimethyl-4-phenyl-3-imidazoline 3-oxide is oxidized the CH3CO group is cleaved to give the 5H-imidazole 1,3-dioxide.
3.  Stable nitroxyl radicals were obtained when the 1-hydroxy-2-oximiaoethyl-2,4,5,5-tetrasubstituted 3-imidazoline 3-oxides are oxidized.
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7.
1.  The ellipsoids of polarizability of dimethylsulfone, sulfuryl chloride, and methanesulfonyl chloride were determined, and the nonadditivity of the parameters of the bonds in the sulfonyl chloride group was demonstrated.
2.  Substituted methane sulfonyl chloride exist in gauche conformations.
3.  In benzenesulfonyl chloride and a series of its para-substituted derivatives, the aryls are situated in the C-S-Cl plane; the para-nitro group induces a 35° rotation.
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8.
1.  The reaction of 6-nitro-2,9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with alcohols and alcoholates leads to remplacement of the nitro group by the corresponding alkoxy group.
2.  The reaction proceeds with either a complete (for the case of the alcoholates) or predominant (for the case of alcohols) inversion of the configuration at the substitution center.
3.  The reaction proceeds via the intermediately formed bicyclic immonium cation.
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9.
1.  It has been shown that 2-bromo-l,3,2-dioxaarsenanes exist in chair conformation with axially oriented As-Br bonds.
2.  Polarity and polarizability parameters have been found for the As-O and As-Br bonds in 2-bromo-l,3,2-dioxaarsenanes.
3.  The so-called -effect is stronger in the O2AsBr group than in the O2AsCl group.
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10.
1.  Dimethyl, diphenyl, and tetramethylene sulfoxide hydrochlorides react with methylheptenyl, citronellyl, and geranyl acetates to give predominantly the allylic chlorination products.
2.  These findings are preferably to be regarded as involving AdE reactions between the weakly electrophlic hydroxy and (or) chlorosulfonium cation and the trisubstituted C=C bond in these olefins at the key stage.
3.  The addition of lithium perchlorate has been found to accelerate this reaction.
4.  Sulfoxide hydrobromides are highly selective brominating agents for the terminal grouping in isopropenoid oligoolefins.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1797–1803, August, 1988.  相似文献   

11.
1.  Methanol, containing 10–20 mole % of CH3I, is carbonylated to methyl acetate in the presence of impregnated Eh-zeolite NaX catalyst at 230–250° and atmospheric pressure.
2.  The specific (per gram of Rh) rate of methyl acetate formation is antibatic to the Rh content in the catalyst, it increases with increase in the methanol contact time, and shows little change in the range 230–250°.
3.  The rate of forming the sole secondary product, namely dimethyl ether, decreases with increase in the amount of Rh and the methanol contact time.
4.  CH2I is an astoichiometric component of the reaction.
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12.
1.  The planar alkoxydiazinoxide fragments are shown to have the Z-configuration and be orthogonal to each other by an x-ray structure study of a series of alkoxydiazinoxides.
2.  In the oxydiazinoxide fragments, p- conjugation occurs.
3.  The molecules of the compounds in the crystals studied are joined by hydrogen bonds.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 297–301, February, 1989.  相似文献   

13.
1.  An intermediate alkoxyphosphorane with two pentacoordinated phosphorus atoms was isolated and characterized during the reaction of 2,5-bis(diethylaminomethyl)hydroquinone with trialkyl phosphites.
2.  A method has been developed for the synthesis of phosphorylated dihydric phenols.
3.  The triethylether of 3-ethoxy-6-hydroxy-1,4-xylyenediphosphonic acid was prepared by the interaction of 2,5-bis(diethylaminomethyl)hydroquinone with diethylphosphorous acid in the presence of triethyl phosphite.
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14.
To mitigate CO2 discharged from thermal power plants, studies on CO2 fixation by the photosynthesis of microalgae using actual exhaust gas have been carried out. The results are as follows.
1.  A method is proposed for evaluating the maximum photosynthesis rate in the raceway cultivator using only the algal physical properties;
2.  Outdoor cultivation tests taking actual flue gas were performed with no trouble or break throughout 1 yr using the strain collected in the test;
3.  The produced microalgae is effective as solid fuel; and
4.  The feasibility studies of this system were performed. The system required large land area, but the area is smaller than that required for other biomass systems, such as tree farms.
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15.
Presently, a large variety of layered materials are synthesized that are able to intercalate neutral guest molecules or to exchange inorganic and organic ions for interlayer ions. Several of these materials are also found as minerals.The intracrystalline reactivity of a few selected compounds will be described and compared to clay minerals:
–  - intercalation into crystalline silicic acids;
–  - reactions of phosphates, arsenates, and sulfates;
–  - reactions of titanates, niobates, and molybdates with long chain alkylammonium ions, and
–  - anion exchange properties of double hydroxides.
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16.
1.  Indium atoms have been obtained in aqueous solutions of univalent indium by pulse radiolysis.
2.  In0 reacts with In+ to form the dimer In 2 + .
3.  The optical characteristics of these particles, the rate constants for their formation and loss, as well as the oxidation-reduction potentials have been determined.
We thank A. G. Egorova for providing the InBr salt.  相似文献   

17.
1.  Depending on the nature of the substituent in the 2 position, l-fluoro-l-(-hydrohexafluoroisopropyl)ethylenes are dehydrofluorinated to either allenes or 1,3-dienes.
2.  It was shown that allylic substitution is possible in the reactions of perfluoroisobutylene with carbanions; the mutual transformations of the allyl and vinyl isomers were studied.
3.  The perfluoroalkenylation product was obtained when perfluoroisobutylene is reacted with ketene acetal.
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18.
1.  Complexes of the REE, Y, and Sc with hydroxyethylethylenediaminetriacetic acid have been isolated in solid form. The hydrate compositions of the complexes have been determined.
2.  The La and Pr complexes form hydrates of different compositions. The LnL hydrates form slightly nonisostructural groups in the series La-Lu.
3.  According to thermographic analysis data, the hydrate water in the LnL·nH2O complexes of different hydrate compositions is not bonded with the same firmness.
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19.
1.  Study has been made of the kinetics of the-elimination of alcohol from 3-carbethoxy-4-ethoxy-2-pentanone in benzene and under the catalytic action of acetic acid.
2.  This reaction involves formation of a complex between substrate and acetic acid.
3.  The equilibrium constant for the reaction of forming the complex between substrate and acetic acid, and the rate constant for complex formation, have both been determined.
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20.
1.  Following the CNDO/2 approximation to the SCF MO LCAO method, electronic parameters have been calculated for the molecules and ions of various nitro compounds.
2.  Calculated values of the dipole moment and enthalpy of atomization proved to be in satisfactory agreement with the experimentally determined values, the maximum deviation between them amounting to 1.4% for the aromatic systems.
3.  The nitro compound parameters most sensitive to change in the intramolecular interaction are the C-N bond energy and the charges on the carbon and halide atoms.
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