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1.
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   

2.
1.  Nitroxyl biradicals of the triazine, N,N-bis(triazinyl)ethylenediamine, N,N-bis(triazinyl)piperazine, and s-nitropyrimidine series have been prepared.
2.  The ESR spectra of liquid and frozen solutions of these biradicals have been obtained and N. - O group separations calculated.
3.  Toluene solutions of (II), (V), (VI), and (X) biradicals contain at least four different conformations, each with its own value of the exchange integral.
4.  In one of the biradical (V) conformations, spin interaction exchange is through the chain of atoms linking the N.-O fragments.
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3.
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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4.
1.  Nonsterically hindered primary arylamines react with hexafluoroacetone benzenesulfonyl- and trifluoroacetylimines to give stable gem-diamino compounds.
2.  The presence of substituents at the nitrogen of the arylamine destabilizes these gem-diamino compounds, with the formation of C2- and C4-alkylation products. With hexafluoroacetone trifluoroacetylimine, C2-alkylation is accompanied by heterocyclization to give 1-substituted 2,4,4-tris(trifluoroacetyl)-1,4-dihydroquinazolines.
3.  N,N-Dialkylanilines are regioselectively alkylated at C4.
For previous communication, see [1].  相似文献   

5.
1.  The authors have studied the formation of electron and hole paramagnetic centers in gamma-irradiated magnesium hydroxide and oxide with various degrees of dehydration.
2.  Rise in the temperature of preliminary heat treatment of the magnesium oxide causes an increase in the radiation-chemical yield of FS + centers and a decrease in that of V su centers.
3.  The thermal stability of paramagnetic centers in magnesium oxide increases as the hydroxyl group content decreases.
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6.
Ethylene-olefin copolymers differ from other polyethylenes in that:
there is no long chain branching;
short chain branching is determined by the comonomer unit;
the molecular mass distribution is sharp;
the side chain distribution on different molecules is broad;
the sequential distribution of branching is very broad along the molecular chains, which becauses a multi-peak lamella distribution, and a multi-peak melting heat.
With the help of a cross-fractionation method we interpreted the differences of the experimental data, according to the molecular mass fractionation and the branching received.  相似文献   

7.
1.  New cationic o-tolyl and o-fluorophenyl complexes of Ni containing Ph3P, MeCN, or THF ligands have been synthesized.
2.  Reaction of these compounds with potassium carboxylates gave the novel o-tolyl and o-fluorophenylbis(triphenylphosphinyl)nickel carboxylates.
3.  According to19F NMR data o-tolylbis(triphenylphosphinyl)nickel p-fluorobetizoate contained a highly polarized Ni-O bond.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 166–170, January, 1988.  相似文献   

8.
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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9.
1.  The hydrolysis rate of N-benzoylanthranilic acid was studied at a KOH concentration of 2.2–44.6% and a temperature of 25–95°.
2.  The limiting step of the process is the reaction of the singly ionized form of the reagent with a molecule of water.
3.  The equilibrium constant for the addition of hydroxyl ion to the carbonyl atom of the amido group of N-benzoylanthranilic acid is 267, and the true rate constant for the reaction of the ionized form with a molecule of H2O at 25° is 0.13 min–1.
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10.
1.  Replacing Na+ ions by Ca2+in zeolites leads to a significant shift of the region in which thermally stimulated polarographic [TSD] current peaks appear toward higher temperatures.
2.  Reducing the cation content in zeolites leads to a decrease in the intensity of TSD currents.
3.  The data obtained-can be explained by the differences in the distributions of the cations between different crystallographic positions in the zeolite lattices.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 1969–1972, September, 1988.  相似文献   

11.
1.  The13C NMR spectra of several 1-alkoxy(phenoxy)-2-phenoxycyclopropanes have been studied.
2.  The configurations of substituted cyclopropanediol ethers have been established with the aid of1H and13C NMR spectroscopy.
  相似文献   

12.
1.  The authors suggest a model to explain the axial symmetry of the hole center V in magnesium oxide.
2.  Using the model they consider the possible alternatives for localization of the hydroxyl groups of the hole center.
3.  In analytic form, they express the values of the g factors for the V center in terms of the parameters of the method of molecular orbits. The experimental values of the g factors can be explained if we assume localization of one or two hydroxyl groups in the first or second layer from the O radical ion in the MgO lattice.
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13.
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.
  相似文献   

14.
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   

15.
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.
  相似文献   

16.
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.
  相似文献   

17.
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.
  相似文献   

18.
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.
  相似文献   

19.
1.  The kinetics of the Cannizzaro reaction of benzaldehyde in aqueous KOH solution have been studied spectrophotometrically, working at 25°C and at concentrations ranging from 19.1 to 37.9%.
2.  Reaction proceeds through the formation of an activated complex consisting of the doubly ionized and the un-ionized forms of benzaldehyde and the hydroxide cation.
3.  The spectrophotometric data and the kinetic data have been combined to give an estimate of the benzaldehyde ionization constant in aqueous KOH solution at 25°C.
4.  Analysis of the kinetic data for benzaldehyde reduction by formaldehyde has shown the activated complex for this reaction to be composed of an un-ionized benzaldehyde molecule and a doubly ionized formaldehyde molecule, with or without participation of the hydroxide cation.
  相似文献   

20.
1.  The adsorption properties with respect to benzene vapors and the pore structure of carbon adsorbents with almost maximum development of the microporosity were studied.
2.  The position of the micropore volume distribution curves whose maxima correspond to a size (halfwidth) of 1.2–1.4 nm and micropore volumes 1.5 cm3/g is a characteristic feature of the adsorbents studied. The difference between ordinary active carbons and the active carbons investigated is only quantitative in the values of the parameters of the Dubinin-Stockley adsorption equation.
3.  The adsorption isotherms are described by the adsorption equation from the theory of volume filling of micropores in a wide range of equilibrium relative pressures and temperatures of 293–353 K with totally satisfactory precision.
4.  The question of the upper limit of the micropores of carbon adsorbents is discussed.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 977–983, May, 1988.  相似文献   

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