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  • 1960-1964  (21)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 184 (1962), S. 156-162 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 410-413 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-(o-hydroxycyclohexyl)-ethylenediamine-N,N′N′-triacetic acid has been investigated as a complexing agent for 7 metal cations by different methods. The stability constants of these complexes are compared with those of ethylenediamine-tetracetic acid and hydroxyethylenediamine-tetracetic acid which do not contain a cyclohexane ring. The latter is found to exert a considerable stabilizing effect.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 842-847 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the solutions of some double cyanides MNi(CN)4 (M = Cu2+, Cd2+, Zn2+) in ammonia clathrates can be obtained with benzene which are of the type of HOFMANN's compound {Ni(CN)2NH3C6H6}. The conditions of formation of these new clathrates have been studied and their structure is discussed. The dry salt [Cd(NH3)6] [Ni(CN)4] has been degraded to CdNi(CN)4, the reaction having been followed by means of tensiometric measurements; thereby the triammonate has been found to be the only intermediate.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1086-1112 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrahydroxytriphenylmethane compounds (aurine dyes and their reduction products) deriving from pyrocatechol are converted easily into deeply coloured substances which can be reduced to colourless leuco-compounds, the reduction and re-oxidation being thermodynamically reversible and furnishing a platinum electrode with a well defined potential. It is shown that these new dyes have the structure of dihydroxyfluorene quinones and diaminofluorene quinones; they are the first fluorene quinones ever described in literature. Several of these substituted fluorene quinones have been obtained in a pure, crystalline state and are characterized by analysis, UV. absorption spectra, IR.-spectra, acid-base indicator behaviour, their oxidation-reduction potential and their ability to form metal complexes.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 45 (1962), S. 2601-2612 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: With a rapid flow apparatus the investigation of the simple protonation of WO42- was achieved (pK1 + pK2 = 8,1, both H+ being added almost simultaneously). The rapid condensation which follows the protonation leeds during the first decisecond to a product of Z = 1.25, probably H5W4O163-. A few minutes later, a new preequilibrium is established with (according to Sasaki) HW6O215- (Z = 1.167) as practically the only polynuclear product present. The final equilibrium is reached only very slowly.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1365-1390 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pure salts Na2S2, K2S2, K2S3, Na2S4, K2S4 and K2S5 have been prepared. Titration curves of these polysulfides in aqueous solution have been obtained with a special streaming apparatus, with which the mixing of the polysulfide solution with HCl and the pH determination of the fresh mixture is accomplished within 10-2 seconds. This time is too short for decomposition of the protonated polysulfide anions into sulfur and monosulfide or H2S respectively to occur. With K2S5 the buffer regions S52- ⇄ HS5- ⇄ H2S5 were obtained readily, furnishing the pK's of H2S5. The solutions of the lower polysulfides, however, do not contain simply the anions present in the lattice of the solid salt. As soon as the solid salts are dissolved disproportionation reactions take place giving rise to mixtures. From the protonation curves of these mixtures - taken with the streaming device mentioned - their composition can be deduced, and it was found that all solutions contain the ions OH-, SH-, S42- and S52-. The ions S22- and S32- were never detected. The equilibrium between mono-, tetra- and pentasulfide has been elucidated and the pK's of H2S4 have been obtained. The results have been checked with photometric measurements on the polysulfide solutions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 46 (1963), S. 2613-2628 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The total concentration of dissolved mercury in equilibrium with solid HgS and in the presence of excess sulfide (present in the form of H2S, HS- and S2- has been determined radiochemically and gravimetrically. The difficult problem of the clean separation of the precipitated HgS from the solution could be solved by very slow filtration of large quantities of the suspension through a small porous plate under constant pressure. The solubility at a constant concentration of excess sulfide (=0,019 molar) as a function of pH is demonstrated in figure 1. The solubility is due to the complex Hg(SH)2 below pH 5, the complex HS-Hg-S- between pH 6 and 8, and the complex HgS22- above pH 9. The solubility produce of black HgS, the stability constants of the complexes, and the two acidity constants of Hg(SH)2 are given in the last section of the paper.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 47 (1964), S. 266-271 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The acidity of the HS- anion is considerably smaller than had been concluded in the extensive investigations of 1946 to 1950. The results obtained 40 years earlier are much nearer the truth. The two pK values of H, S in 1MKC1 and at 20°C are 6,88 ± 0,02 and 14,15 ±0,05.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 45 (1962), S. 1454-1457 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the binuclear complex [(NH3)] Cr—Oh—Cr(NH3)4—CH2—CH2—\documentclass{article}\pagestyle{empty}\begin{document}$ \mathop {\rm N}\limits^{(+)} $\end{document}H36+, which has been obtained in the form of the well crystallised hexachloride is described. On adding alkali (titration in a rapid flow apparatus) the OH-bridge (pK = 6,36) is first deprotonated and the terminal ammonium group (pK = 8,42) afterwards. Both deprotonation products are blue and highly unstable, hydrolysing rapidly to the hydroxo-erythro ion and ethylenediamine.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 46 (1963), S. 1390-1400 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The equilibria between iron(III), acethydroxamic acid, benzhydroxaminc acid, desferri-ferrioxamin B and their iron complexes have been elucidated by combining redox potentials, pH and photometric measurements. For the results see section f above.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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