Disproportionation of some alkali metal chlorites in the solid phase

Thermal behaviours of some alkali metal chlorites were studied under dynamic and isothermal conditions and some physical data of the chlorites were also determined. It was found that these chlorites disproportionate into chlorate and chloride in the solid phase without any measurable evolution of gas. The disproportionations were strongly exothermic. The values of the activation energies for the disproportionation reactions were found to be much smaller than the dissociation energy required for the rupture of the Cl-O bond. It was concluded that the disproportionations of alkali metal chlorites take place by rearrangement inside the lattice, without formation of atomic oxygen.

---

Zusammenfassung Das thermische Verhalten einiger Alkalimetallchlorite wurde unter dynamischen und isothermen Bedingungen untersucht und einige physikalischen Daten der Chlorite bestimmt. Es wurde festgestellt, da\ diese Chlorite in fester Phase ohne me\bare Gasentwicklung zu Chloraten und Chloriden disproportionieren. Der Disproportionierungsvorgang war streng exotherm. Die für die Disproportionierungsreaktion festgestellten Werte der Aktivierungsenergie waren viel niedriger als die zur Spaltung der Bindung Cl-O benötigte Dissoziationsenergie. Es wurde gefolgert, da\ die Disproportionierung von Alkalimetallchloriten durch Umordnung im Inneren des Gitters ohne Bildung von atomarem Sauerstoff erfolgt.

---

Résumé Le comportement thermique de chlorites de métaux alcalins a été étudié en conditions de chauffage dynamique et isotherme. Quelques données physiques des chlorites ont aussi été déterminées. Il a été observé que ces chlorites se dismutent en phase solide en chlorate et chlorure sans dégagement mesurable de gaz. La dismutation est fortement exothermique. Les valeurs des énergies d'activation de la réaction de dismutation sont bien inférieures à l'énergie de dissociation nécessaire à la rupture de la liaison Cl-O. On en conclut que la dismutation des chlorites des métaux alcalins s'effectue par réarrangement à l'intérieur du réseau sans formation d'oxygène atomique.

---

. , - . . , , , l — . , .

---

---

We thank Miss E. Szcs for assistance in the experimental work.     

Sulfur dioxide mediated one-pot, three- and four-component syntheses of polyfunctional sulfonamides and sulfonic esters: study of the stereoselectivity of the ene reaction of sulfur dioxide

The ene reaction of sulfur dioxide with enoxysilanes or with allylsilanes generates silyl sulfinates that can be brominated (Br(2) or NBS) or chlorinated (NCS or Cl(2)) to produce the corresponding sulfonyl halides. They react with primary and secondary amines or alcohols to give the corresponding sulfonamides and sulfonic esters, respectively. The hetero-Diels-Alder addition of sulfur dioxide to 1-oxy- or 1,3-dioxy-1,3-dienes generates zwitterions that add to enoxysilanes or allylsilanes giving silyl sulfinates that can be converted in situ into polyfunctional sulfonamides or sulfonic esters. This realizes quick access to libraries of complicated sulfonamides and sulfonic esters applying one-pot, three- and four-component methods.     

Conductivities and silver electrode polarization resistance of solid electrolyte ceramics from ZrO2-Y2O3 powder synthesized in air plasma

Ceramic specimens have been obtained from the powder of ZrO₂-7.5 mol% Y₂O₃ having a specific surface area of 30 m²/g synthesized in air plasma. The novelty of this research lies in the fact that the plasma process makes it possible to prepare so-called nanopowders with a particle size less than 100 nm, possessing specific physical, chemical and technological properties. The sintered density of the specimens was 94–96% of the theoretical value, 6.001 g/cm³. The X-ray diffraction pattern of the specimens corresponded to a face-centered cubic lattice. Impedance in the frequency range of 100 Hz–15 MHz and d.c. polarization curves in a potential range of −10 to 10 mV were measured in the temperature range 200–850 °C in heating and cooling cycles. The intragrain, the grain boundary and the total bulk conductivities, the electrode polarization resistance and their activation energies were determined. The thermal stability of the studied system was proved in three measurement series up to 600–850 °C in heating and cooling cycles. The results obtained have shown that the conductivity of ZrO₂-7.5 mol% Y₂O₃ ceramics is not solely a function of temperature, but also depends on the previous thermal state of the ceramics. Received: 16 October 1997 / Accepted: 19 January 1998     

N,N'-ethylenebis(pyridoxylideneiminato) and N,N'-ethylenebis(pyridoxylaminato): synthesis, characterization, potentiometric, spectroscopic, and DFT studies of their vanadium(IV) and vanadium(V) complexes

The Schiff base N,N'-ethylenebis(pyridoxylideneiminato) (H(2)pyr(2)en, 1) was synthesized by reaction of pyridoxal with ethylenediamine; reduction of H(2)pyr(2)en with NaBH(4) yielded the reduced Schiff base N,N'-ethylenebis(pyridoxylaminato) (H(2)Rpyr(2)en, 2); their crystal structures were determined by X-ray diffraction. The totally protonated forms of 1 and 2 correspond to H(6)L(4+), and all protonation constants were determined by pH-potentiometric and (1)H NMR titrations. Several vanadium(IV) and vanadium(V) complexes of these and other related ligands were prepared and characterized in solution and in the solid state. The X-ray crystal structure of [V(V)O(2)(HRpyr(2)en)] shows the metal in a distorted octahedral geometry, with the ligand coordinated through the N-amine and O-phenolato moieties, with one of the pyridine-N atoms protonated. Crystals of [(V(V)O(2))(2)(pyren)(2)].2 H(2)O were obtained from solutions containing H(2)pyr(2)en and oxovanadium(IV), where Hpyren is the "half" Schiff base of pyridoxal and ethylenediamine. The complexation of V(IV)O(2+) and V(V)O(2) (+) with H(2)pyr(2)en, H(2)Rpyr(2)en and pyridoxamine in aqueous solution were studied by pH-potentiometry, UV/Vis absorption spectrophotometry, as well as by EPR spectroscopy for the V(IV)O systems and (1)H and (51)V NMR spectroscopy for the V(V)O(2) systems. Very significant differences in the metal-binding abilities of the ligands were found. Both 1 and 2 act as tetradentate ligands. H(2)Rpyr(2)en is stable to hydrolysis and several isomers form in solution, namely cis-trans type complexes with V(IV)O, and alpha-cis- and beta-cis-type complexes with V(V)O(2). The pyridinium-N atoms of the pyridoxal rings do not take part in the coordination but are involved in acid-base reactions that affect the number, type, and relative amount of the isomers of the V(IV)O-H(2)Rpyr(2)en and V(V)O(2)-H(2)Rpyr(2)en complexes present in solution. DFT calculations were carried out and support the formation and identification of the isomers detected by EPR or NMR spectroscopy, and the strong equatorial and axial binding of the O-phenolato in V(IV)O and V(V)O(2) complexes. Moreover, the DFT calculations done for the [V(IV)O(H(2)Rpyr(2)en)] system indicate that for almost all complexes the presence of a sixth equatorial or axial H(2)O ligand leads to much more stable compounds.     

Countable Fréchetα 1-spaces may be first countable

It is shown to be consistent that countable, Fréchet, ₁-spaces are first countable. The result is obtained by using a countable support iteration of proper partial orders of length ₂.The research of both authors is partially supported by NSERC     

Pressurized liquid extracts from Spirulina platensis microalga. Determination of their antioxidant activity and preliminary analysis by micellar electrokinetic chromatography

In this work, different extracts from the microalga Spirulina platensis are obtained using pressurized liquid extraction (PLE) and four different solvents (hexane, light petroleum, ethanol and water). Different extraction temperatures (115 and 170 degrees C) were tested using extraction times ranging from 9 to 15 min. The antioxidant activity of the different extracts is determined by means of an in vitro assay using a free radical method. Moreover, a new and fast method is developed using micellar electrokinetic chromatography with diode array detection (MEKC-DAD) to provide a preliminary analysis on the composition of the extracts. This combined application (i.e., in vitro assays plus MEKC-DAD) allowed the fast characterization of the extracts based on their antioxidant activity and the UV-vis spectra of the different compounds found in the extracts. To our knowledge, this work shows for the first time the great possibilities of the combined use of PLE-in vitro assay-MEKC-DAD to investigate natural sources of antioxidants.     

Sealed Sources. Some Aspects of Development and Production in the German Democratic Republic

Industrially advanced countries and inereasingly also agricultural countries today use radioisotopes as labelled compounds or scaled sources in order to solve their scientific and technological problems.     

Partial control of delay-coordinate maps

Nonlinear Dynamics - Delay-coordinate maps have been widely used recently to study nonlinear dynamical systems, where there is only access to the time series of one of their variables. Here, we...     

Sonocatalytic decolorization of methylene blue from aqueous media by La:ZnO/GO nanocomposites

Research on Chemical Intermediates - The collaboration of graphene oxide and a rare earth element dopant has a significant effect on the catalytic performance of zinc oxide nanoparticles (ZnO). For...