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Finansministern i domkapitlet : Ernst Wigforss som ledamot av Göteborgs domkapitel 1918−1936
Ernst Wigforss (1881−1977) was Minister of Finance in Sweden 1925−26, 1932−36, and 1936−49, and one of the great ideologists of Swedish SocialDemocracy. During 1918−36 he was also a member of the Chapter in the Diocese of Gothenburg, Church of Sweden.Before 1937, lecturers in the old grammar schools were ex officiomembers of the diocesan chapter. The agnostic Wigforss took his seat in the chapter
Introduction / Einleitung
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Göteborgs stifts herdaminne 1620–1699 III : Fässbergs, Älvsyssels södra och norra kontrakt
Kyrkohistorisk årsskrift 2016
Hilding Pleijels ”genusperspektiv”
Recension : Anders Dillmar. Harald Göransson och kyrkomusikens förändring i Sverige under 1900-talets andra hälft (fyra band)
Recension : Elisabeth Hallgren Sjöberg, Såsom en slöja. Den kristna slöjan i en svensk kontext
Recension : Hartmut Ludwig & Eberhard Röhm in Verbindung mit Jörg Thierfelder (Hg.), Evangelisch Getauft – Als ”Juden” Verfolgt. Theologen jüdischer Herkunft in der Zeit des Nationalsozialismus. Ein Gedenkbuch
Reaction of Peroxomonosulfate Radical with Manganese(II) in Acidic Aqueous Solution. A Pulse Radiolysis Study
The reaction between the SO5– radical and MnII has been proposed to be the most important process for regeneration of MnIII in the MnIII/II-catalysed autoxidation of SIV in acidic aqueous solution. In the present study, the second-order rate constant for this reaction has been determined at pH 3. 0 and 10 mmol dm–3 ionic strength by use of pulse radiolysis. The study was performed in the presence The reaction between the SO5– radical and MnII has been proposed to be the most important process for regeneration of MnIII in the MnIII/II-catalysed autoxidation of SIV in acidic aqueous solution. In the present study, the second-order rate constant for this reaction has been determined at pH 3. 0 and 10 mmol dm–3 ionic strength by use of pulse radiolysis. The study was performed in the presence
Kinetics of Carbon Monoxide Exchange in Chloro and Bromo Carbonyl Complexes of Palladium(II) and Platinum(II)
Carbonyl exchange between [MX3(13CO)]–(MX = PdCl, PtCl or PtBr) and 12CO has been studied by IR and 13C NMR spectroscopies as a function of temperature. The exchange is first-order in both CO and complex concentration, and the activation entropies are negative, suggesting an associative reaction mechanism. There is a small solvent effect, but no chloride dependence. Activation parameters and rate Carbonyl exchange between [MX(3)((CO)-C-13)](-) (MX = PdCl, PtCl or PtBr) and (CO)-C-12 has been studied by IR and C-13 NMR spectroscopies as a function of temperature. The exchange is first-order in both CO and complex concentration, and the activation entropies are negative, suggesting an associative reaction mechanism. There is a small solvent effect. but no chloride dependence. Activation para
Names and symbols of transfermium elements (IUPAC recommendations 1994)
The Transfermium Working Group (TWG) was set up in 1986 under the joint auspices of the International Union of Pure and Applied Chemistry (IUPAC) and the International Union of Pure and Applied Physics (IUPAP). Its conclusions, duly endorsed by IUPAC and IUPAP, were published in the following three reports: 1. Criteria that must be satisfied for the discovery of a new chemical element to be recognThe Transfermium Working Group (TWG) was set up in 1986 under the joint auspices of the International Union of Pure and Applied Chemistry (IUPAC) and the International Union of Pure and Applied Physics (IUPAP). Its conclusions, duly endorsed by IUPAC and IUPAP, were published in the following three reports:1. Criteria that must be satisfied for the discovery of a new chemical element to be recogni
Managing value appropriation in buyer-supplier relationships : The role of commercial decision resources
The resource-based view explains firms’ value appropriation in buyer-supplier relationships by pointing to sustained differences in economic efficiency across firms. Firms with more efficient resources create more value than competitors, which in turn provides a “protective cushion” against price-/quality competition. However, just as firms may differ in the economic efficiency of their resources
Kinetics and Mechanism for Oxidation of Dissolved Sulfur Dioxide by Tetracyanodichloroplatinate(IV) in Acidic Aqueous Solution and for Formation and O-S Linkage Isomerization of Sulfitotetracyanochloroplatinate(IV)
Oxidation of SO2.nH2O/HSO3-/SO32- by Pt(CN)4Cl22- has been studied at 25-degrees-C and 1.0 M ionic strength in acidic aqueous solution by use of stopped-flow spectrophotometry. The stoichiometry of the reaction is 1:1 according to Pt(CN)4Cl22- + HSO3 + H2O --> Pt(CN)42- + 2Cl- + HSO4- + 2H+. It is first-order with respect to both [Pt(IV)] and [S(IV)]. The pH-dependence in the region 0.3 < pH < 4.5
Kinetics and Mechanism for the Redox Reaction between Hexaaquathallium(III) and Sulfur Dioxide in Acidic Aqueous Solution
Oxidation of dissolved sulfur dioxide, SO2·nH2O, HSO3– and SO32–, by hexaaquathallium(III) has been studied in acidic aqueous solution with ionic strength 1.0 mol dm–3 at 25 °C. The stoichiometry of the reaction has been determined: [Tl(H2O)6]3++ SO2(aq)+ 2H2O →[Tl(H2O)6]++ HSO4–+ 3H+. The kinetics has been studied by use of stopped-flow spectrophotometry under pseudo-first-order conditions with eOxidation of dissolved sulfur dioxide, SO2·nH2O, HSO3– and SO32–, by hexaaquathallium(III) has been studied in acidic aqueous solution with ionic strength 1.0 mol dm–3 at 25 °C. The stoichiometry of the reaction has been determined: [Tl(H2O)6]3++ SO2(aq)+ 2H2O →[Tl(H2O)6]++ HSO4–+ 3H+. The kinetics has been studied by use of stopped-flow spectrophotometry under pseudo-first-order conditions with e
New Methods for Synthesis of Platinum(II) Dimethyl Sulfide Complexes
Different methods for the synthesis of anionic dimethyl sulfide platinum complexes of the type Q[PtCl3(Me2S)] (Q = triphenylbenzylphosphonium, Ph3PBzl, or tetrabutylammonium, BU4N) and [Pt(mu-Cl)Cl(Me2S)]2 are reported. The compounds Q[PtCl3(Me2S)] were prepared by interaction of [PtCl4]2- with an excess of Me2S in non-aqueous media, reduction of [PtCl5(Me2S)]- with hydrazine sulfate, bridge-split
Kinetics and Mechanism for Manganese-Catalyzed Oxidation of Sulfur(IV) in Aqueous Solution
The kinetics for manganese-catalyzed autoxidation of sulfur(IV) (SO2.nH2O, HSO3-, SO32-) in aqueous solution has been studied spectrophotometrically at 25-degrees-C, 1 < pH < 4, [S(IV)] almost-equal-to 2.3 X 10(-5) M, 1 X 10(-6) M less-than-or-equal-to [Mn(II)] less-than-or-equal-to 1.5 X 10(-3) M, [Mn(III)] less-than-or-equal-to 4 X 10(-8) M, [O2] almost 2.5 X 10(-4) M, and low ionic strength. In
Phenylation of Platinum(II) Thioether Complexes by Tetraphenylborate(III) in Solid State and Nitromethane Solution
Platinum(II) complexes of the type [Pt(thioether)2Cl]+(thioether = dimethyl sulfide, thioxane) are capable of abstracting a phenyl group from the BPh4 counterion with formation of trans[Pt(thioether)2ClPh] compounds. Thermal reactions proceed both in the solid phase and in nitromethane solution at elevated temperature and have preparative importance. Phenylation of the Pt(II) centre also occurs inPlatinum(II) complexes of the type [Pt(thioether)2Cl]+(thioether = dimethyl sulfide, thioxane) are capable of abstracting a phenyl group from the BPh4 counterion with formation of trans[Pt(thioether)2ClPh] compounds. Thermal reactions proceed both in the solid phase and in nitromethane solution at elevated temperature and have preparative importance. Phenylation of the Pt(II) centre also occurs in
Dissociative Reactions to the San Francisco Bay Area Earthquake of 1989
This study systematically evaluated the psychological reactions of a non-clinical population to the October 1989 Bay Area earthquake. Within a week of the earthquake, a checklist of anxiety and dissociative symptoms was administered to a representative sample of approximately 100 graduate students and faculty members from two different institutions in the Bay Area. A follow-up study was conducted