Influence of the pyridine methyl substituent position on the chemical changes of the NCS groups in the thermal decomposition of coordination compounds of the type Cu(NCS)2L2

The influence of the position of the CH₃ group in picoline and lutidine ligands on the degree of chemical change of the NCS groups in coordination compounds of the type Cu(NCS)₂L₂ (whereL=2-, 3- and 4-picoline, and 2,3-, 2,4-, 2,5-, 2,6-, 3,4- and 3,5-lutidine) is dealt with. The most marked effect of the CH₃ group is found to be exerted in position 4. This effect of the methyl group on the degree of chemical change points to the mutual influence of the ligands in coordination compounds of Cu(II).

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Zusammenfassung Der Artikel befaßt sich mit dem Einfluß der Lage der CH₃ Gruppe in Pikolinen und Lutidinen als Liganden auf den Grad der chemischen Änderungen der Gruppen NSC in Koordinationsverbindungen des Typs Cu(NCS)₂L₂ (L=2-, 3- und 4-Pikoline, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- und 3,5-Lutidine). Der ausgeprägteste Effekt der CH₃ Gruppe wurde in der Position 4 beobachtet. Dieser Einfluß der Methylgruppe auf das Ausmaß der chemischen Änderungen deutet auch auf die gegenseitige Wirkung der Liganden in Koordinationsverbindungen von Cu(II).

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Résumé L'article a trait à l'influence de la position du groupe CH₂ dans les picolines et lutidines, en tant que ligands, sur le degré des changements chimiques des groupes SCN dans les composés de coordination du type Cu(SCN)₂L₂ (L=2-, 3 et 4-picoline, 2,3-, 2,4-,2,5-, 2,6-, 3,4- et 3,6-lutidine). L'effet le plus prononcé du groupe CH₃ s'observe en position 4. Cette influence du groupe méthyle sur le degré des changements chimiques indique aussi l'influence mutuelle des ligands dans les composés de coordination du Cu(II).

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- , , NCS Cu(NCS)₂,L₂, L=2-, 3- 4- , 2.3-, 2.4-, 2.5-, 2.6-, 3.4- 3.5-. , 4. Cu(II).

     

Geometrical structure of yttrium and metal-bromine complexes in solution: limitations of extended X-ray absorption fine structure analysis (EXAFS)

An extensive study on the appearance of multi-electron features in the X-ray absorption spectra of several yttrium(III)-based compounds has been performed. The existence of a multi-electron transition of non-negligible intensity within the extended X-ray absorption fine structure (EXAFS) region of the Y K-edge spectra has been proven. The impact of such features in the EXAFS analysis is made evident for aqueous solutions of YBr3 x 6H2O in liquid and glassy states in the concentration range 0.005-2.0 M, in which this transition induces an overestimation in the coordination numbers derived from EXAFS. We have performed theoretical computation of cross-sections for the double-electron processes at the K-edge of both Y and Br. These computations have been applied to the experimental EXAFS K-edge spectra of both Y and Br in several solids and in aqueous solutions. While in the case of Y K-edge spectra the presence of such multi-electron transitions was seen to seriously affect the standard EXAFS analysis, its influence in the case of Br K-edge spectra was determined to be negligible.     

Nachweis isomerer Phenole und Nitroaniline,von Naphthylamin und Anilin

Zusammenfassung Die mit diazotiertem p-Nitranilin hergestellten Tetrazoverbindungen von Phenolderivaten geben mit Magnesium in alkalischem Mediumfarbige Komplexe. Die Farbe des Komplexes ist verschieden bei substituierten und nicht substituierten bzw. verschieden substituierten Phenolen. Damit kann man Phenol-, Kresol- und Chlorphenol-Isomere bzw. 2,4- und 2,6-Dichlorphenol unterscheiden.Beim Diazotieren von Nitranilin und Kuppeln mit Anilin entstehen. Indikatorsäuren; p-Nitranilin bildet die stärkste Indikatorsäure, m-Nitranilin die schwächste. Auf dieser Grundlage können alle drei Isomeren nebeneinander nachgewiesen werden. Außerdem bilden die aus p- und o-Nitranilin entstandenen Indikatoren mit Magnesium verschieden gefärbte Nitronsäurekomplexe, während m-Nitranilin, das zur Nitronsäuretautomerie nicht befähigt ist, keinen Komplex bildet.Naphthylamine geben mit diazotiertem p-Nitranilin in wäßrigem. Medium eine Indikatorbase, Anilin eine Indikatorsäure. In alkoholischem Medium führt-Naphthylamin bei Kupplung von diazotiertem p-Nitranilin zu einem amphoteren Säure-Base-Indikator, aber-Naphthylamin und Anilin zu Indikatorsäuren. Damit kann man Naphthylamin und Anilin nebeneinander nachweisen. Kuppelt man Phenyldiazoniumchlorid mit Naphthylamin, so erhält man mit-Naphthylamin eine starke Indikatorbase, mit- Naphthylamin eine schwache Indikatorbase. Auf der Basis dieser Indikatorwirkung kann man-Naphthylamin neben- Naphthylamin nachweisen.

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Summary The tetrazo compounds of phenol derivatives prepared with diazotizedp-nitraniline yield colored complexes with magnesium in alkaline surroundings. The color of the complexes differs with substituted and non-substituted or variously substituted phenols. It is possible in this way to differentiate phenol, cresol and chlorophenol isomers, and also 2,4- and 2,6-dichlorophenol.Indicator acids result from diazotized nitraniline coupled with aniline;p-nitraniline yields the strongest indicator acid,m-nitraniline the weakest. With this information as a basis, all three isomers can be detected in the presence of each other. In addition, the indicators produced fromp- ando-nitraniline give nitronic acid complexes with magnesium that differ in color, whilem-nitraniline, which is not capable of nitronic acid tautomerism, forms no complex.Naphthylamines gives an indicator base in aqueous medium with diazotizedp-nitraniline, whereas aniline yields an indicator acid. In alcoholic medium, 1-naphthylamine on coupling with diazotizedp-nitraniline produces an amphoteric acid-base indicator, but 2-naphthylamine and aniline yield indicator acids. Naphthylamine and aniline can be detected in this way in the presence of each other. If phenyldiazonium chloride is coupled with naphthylamine, a strong indicator base is obtained with 1-naphthylamine, a weak indicator base with 2-naphthylamine. This indicator action is the basis of the detection of 1-naphthylamine in the presence of 2-naphthylamine.

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Résumé Les composés tétrazoïques des dérivés phénoliques qui se forment avec lap-nitraniline diazotée, donnent avec le magnésium, en milieu alcalin, des complexes colorés. La couleur du complexe diffère suivant que les phénols sont substitués, non substitués ou différemment substitués. On peut ainsi distinguer le phénol, les crésols et les chlorophénols isomères, ainsi que les dichloro-2,4 et -2,6 phénols.En diazotant la nitraniline et en copulant avec l'aniline, des acides indicateurs prennent naissance, lap-nitraniline donnant l'acide indicateur le plus fort, lam-nitraniline le plus faible. En s'appuyant sur ce fait, on peut rechercher les trois isomères en présence les uns des autres. En outre, les indicateurs qui prennent naissance à partir de lap- et de l'o-nitraniline forment avec le magnésium différents complexes colorés acinitrés, alors que lam-nitraniline, qui n'est pas susceptible d'une tautomérie de l'acide nitronique, ne donne pas de complexe.Les naphtylamines donnent avec lap-nitraniline diazotée, en milieu aqueux, une base indicateur et l'aniline, un acide indicateur. En milieu alcoolique, l'-naphtylamine conduit par copulation de lap-nitraniline diazotée à un indicateur acide-base amphotère mais la-naphtylamine et l'aniline à des acides indicateurs. On peut ainsi rechercher la naphtylamine et l'aniline en présence l'une de l'autre. Si l'on copule le chlorure de phenyldiazonium avec la naphtylamine, on obtient avec la forme une base indicateur forte et avec la forme une base indicateur faible. En se fondant sur cette action d'indicateur, on peut rechercher l'-naphtylamine en présence de-naphtylamine.

     

Sandwich structures at oil-water interfaces under alkaline conditions

Equilibrium liquid crystal (LC) layer on an interface between crude oils and water was observed at high pH. This layer is composed mainly of sodium naphthenates produced in situ at the water/oil interface. Transient LC layer was also evolved at the interface of aqueous phase of sodium hydroxide solutions and oleic phase of naphthenic acid (NA) solutions as result of a chemical reaction between NaOH and NA. This chemical reaction causes transport process resulting in a disturbance of the interface. Optical observation of this interface disturbance reviled that the interface covered with LC shows considerably lower flexibility as compared to LC free interface. The LC layer eventually dissolves in the water phase at low oil-to-water ratio, while at high oil-to-water ratio it can form an equilibrium phase, which spreads spontaneously at the oil-water interface.     

Thermodynamic parameters for the molecular inclusion reaction of dulcin with beta-cyclodextrin. spectrofluorimetric determination of dulcin

The inclusion of dulcin in alpha- and beta-cyclodextrin has been studied by fluorescence spectroscopy. To quantitatively describe complex formation between the beta-cyclodextrin and dulcin, an association constant of 290 M(-1) at 21 degrees was obtained. The thermodynamics associated with the complex formation between dulcin and beta-cyclodextrin in aqueous solution has been studied. The obtained value of DeltaG(0) = -13.7 kJ/mole at 21 degrees , together with DeltaH(0) = -33.6 +/- 2.3 kJ/mole and DeltaS(0) = -67.2 +/-8.3 Jmole(-1) K(-1) indicate that dulcin has a very marked tendency to associate with beta-cyclodextrin in water. The inclusion complex of dulcin in beta-cyclodextrin has been used to determine dulein in the range 0.13-5 mug/ml the method has been applied to determine dulcin in soft drinks.     

Hydration of acetylene on Cd2+ exchanged zeolites

The reaction takes place on Cd-containing Lewis sites, whereas the irreversible adsorption and condensation of product acetaldehyde on acidic OH groups of Cd-X, FAU catalyst results in deactivation. Preadsorbed ammonia moderates the deactivation, because it reacts with acetylene, and pyridine homologues are formed which block the accessible OH groups. Since in divalent cationic forms of clinoptilolite no OH groups are generated, Cd-clinoptilolite proved to be a catalyst of permanent activity.

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, Cd, — OH FAU, Cd-X. , .. , OH . OH, Cd- .

     

Properties and analytical applications of the heteropolymolybdates of phosphorus, arsenic, silicon and germanium-IV Determination of phosphomolybdic and silicomolybdic acids via the molybdenum content, with phenylfluorone

Procedures are proposed for the determination of phosphorus and silicon in the ppM range, by extraction of phosphomolybdic and silicomolybdic acids with organic solvent, decomposition of the complex and spectrophotometric determination of its molybdenum content.     

Complex study of nickel skeleton catalysts: V. Study of novel non-pyrophoric nickel skeleton catalysts by derivatograph

The structure and properties of non-pyrophoric skeleton catalysts prepared from NiSi, NiAlSi, NiMg and NiZn alloys have been studied—apart from other thermal methods—by means of the derivatograph.Our experimental results have contributed to the explanation of the non-pyrophoric behaviour of these catalysts. We demonstrated that the desorption of the hydrogen content in our catalysts is not accompanied by the oxidation of active nickel. This oxidation takes place only at higher temperatures, above 200°C, at a rate proportional to the amount of active nickel.Other constituents of the catalysts (adsorbed water, hydroxide content) were also determined from the experimental data. The outstandingly high Mg(OH)₂ content of the NiMg catalyst indicates that its structure is dissimilar: Mg(OH)₂ also acts as support for the catalyst.     

Isotope gas analysis of tritium-labelled organic compounds based on pyrolytical decomposition

Summary A procedure has been developed for the activity measurement of tritium-labelled organic compounds in the gas phase. The organic compounds are pyrolysed in hydrogen carrier gas at 1150° and the decomposition products are swept through a carbon packing in accordance with the principle of the oxygen determination developed byUnterzaucher andBürger. The radioactive gas mixture obtained from the sample is swept by the hydrogen carrier gas flowing continuously through the reactor into a proportional counter tube, after the addition of propanebutane counter gas. By closure of the counter tube at a suitable moment, the radioactive gas is quantitatively trapped in the counter tube. The activity is measured in the limited proportional region. No memory effect occurs. The preparation of the sample requires 12 minutes; the relative standard deviation of analysis is <0.5%.

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Zusammenfassung Ein Verfahren zur Aktivitätsbestimmung bei tritium-markierten organischen Verbindungen in der Gasphase wurde ausgearbeitet. Die organischen Substanzen werden in Wasserstoff als Trägergas bei 1150° pyrolysiert. Die Zersetzungsprodukte werden wie bei der Sauerstoffbestimmung nachUnterzaucher bzw.Bürger über eine Kohleschicht geleitet. Das radioaktive Gas-gemisch aus der Probe gelangt mit dem kontinuierlich strömenden Trägergas in ein Proportionalzählrohr, nachdem Propan-Butan-Zählgas zugesetzt wurde. Man schließt das Zählrohr im richtigen Augenblick, um das radioaktive Gas quantitativ zu erfassen. Die Aktivität wird im Proportionalbereich gemessen. Ein Memory-Effekt tritt nicht auf. Die Vorbereitung der Probe beansprucht 12 Minuten. Die relative Standardabweichung ist kleiner als 0,5%.

     

L X-ray production cross sections, average L shell fluorescence yield and intensity ratios in heavy elements

L X-ray fluorescence cross sections, and intensity ratios were measured for elements in the 70￡Z￡92 atomic range at the excitation energy 59.5 keV using a Si(Li) detector. Furthermore, L X-ray fluorescence cross sections and intensity ratios were calculated for elements in the same range. The average L shell fluorescence yields were derived using experimental L X-ray fluorescence cross sections and theoretical photoionization cross sections. The obtained results were compared with other experimental and theoretical values. This revised version was published online in August 2006 with corrections to the Cover Date.