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  • 1985-1989  (8)
  • 1980-1984  (8)
  • 1970-1974
  • 1950-1954
  • 1935-1939
  • 1988  (8)
  • 1984  (8)
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  • 1985-1989  (8)
  • 1980-1984  (8)
  • 1970-1974
  • 1950-1954
  • 1935-1939
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 18 (1988), S. 245-251 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The e.m.f. of a concentration cell for SO x (x=2,3)-O2 incorporating Nasicon as the main solid electrolyte has been measured in the temperature range 720 to 1080 K. The cell arrangement can be represented as, $$Pt, O'_2 + SO'_2 + SO'_3 \left| {Na_2 SO_4 \left\| {\left. {Nasicon} \right\|} \right.} \right.\left. {Na_2 SO_4 } \right|SO''_3 + SO''_2 + O''_2 , Pt$$ The Na2SO4 acts both as an auxiliary electrode, converting chemical potentials of SO x and O2 to equivalent sodium potentials, and as an electrolyte. The presence of Na2SO4 provides partial protection of Nasicon from chemical reaction with gas mixtures containing SO x . The open circuit e.m.f. of the cell is in close agreement with values given by the Nernst equation. For certain fixed inlet gas compositions of SO2+O2, the e.m.f. varies non-linearly with temperature. The intrinsic response time of the cell to step changes in gas composition is estimated to vary from ∼2.0 ksec at 723K to ∼ 0.2 ksec at 1077K. The cell functions well for large differences in partial pressures of SO3(p″SO 3/p′SO 3≈104) at the electrodes.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 330 (1988), S. 386-387 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions Formation of the uroporphyrin isomers II and IV in urines of patients with AIP can be explained by non-enzymatic self-condensation of PBG. Presence of the coproporphyrin isomers II and IV, however, must be due to enzymatic processes, the nature of which have to be clarified.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental mechanics 24 (1984), S. 232-232 
    ISSN: 1741-2765
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 564 (1988), S. 81-84 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Organo Transition Metal Compounds. 53. Synthesis and Properties of Manganese Tetravinyloxide, Mn(OCH=CH2)4 · 0.5 THFTetrakis(1-Norbornyl)manganese (I) reacts with boiling tetrahydrofuran forming ethylene, norbornane, and manganese tetravinyloxide Mn(OCH=CH2)4 · 0.5 THF (II) as the first manganese tetraalcoxide. The compound was characterized by elementary analysis, the i.r. and 1H n.m.r. spectrum, the effective magnetic moment, and the protolysis products.
    Notes: Tetrakis(1-norbornyl)mangan (I) reagiert mit siedendem Tetrahydrofuran unter Abspaltung von Ethylen und Norbornan zu Mangantetravinyloxid, Mn(OCH=CH2)4 · 0,5 THF (II), als dem ersten bekannt gewordenen Mangan(IV)-alkoxid. Die Verbindung wurde durch Elementaranalyse, das IR- und 1H-NMR-Spektrum, das effektive magnetische Moment und durch die Protolyseprodukte charakterisiert.
    Additional Material: 1 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 50-54 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXVII. About the Existence of 1-Norbornyl Compounds of Tungsten and MolybdenumReactions of WCl6, WCl4, WO2Cl2, WOCl4, MoCl5, and MoO2(acac)2 with 1-Norbornyl lithium (1-NorLi1)) are described. From WCl6 and WCl4 [(1-Nor)2W]n is formed, whereas in dependence of the solvent WO2Cl2 and WOCl4 are transformed into the complexes Li2[1-NorWOCl4] · THF, Li[WOCl4], Li[WO2Cl2], and Li2[WO2Cl2]. MoCl5 and MoO2(acac)2 are reduced with formation of Li[MoCl5], Li[MoO2(acac)2] and Li2[MoO2(acac)2].  -  Stable (1-Nor)4M-derivatives of molybdenum and tungsten, comparable those of 3d-metals (M = Ti—Co) seem not to exist.
    Notes: Es wird über Reaktionen von WCl6, WCl4, WO2Cl2, WOCl4, MoCl5 und MoO2(acac)2) mit 1-Norbornyllithium (1-NorLi1)) berichtet. Ausgehend von WCl6 und WCl4 wird [(1-Nor)2W]n gebildet, während WO2Cl2 und WOCl4 je nach Lösungsmittel Komplexe der Formeln Li2[1-NorWOCl4] · THF, Li[WOCl4], Li[WO2Cl2] und Li2[WO2Cl2] ergeben. MoCl5 und MoO2(acac)2 werden zu Li[MoCl5], Li[MoO2(acac)2] und Li2[MoO2(acac)2] reduziert. - Den stabilen (1-Nor)4M-Derivaten der 3d-Metalle (M = Ti—Co) vergleichbare Verbindungen des Molybdäns und Wolframs scheinen nicht zu existieren.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 511 (1984), S. 89-94 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXVIII. Reactions of Dibenzyl Manganese with Oxygene(C6H5CH2)2Mn · C4H8O2 reacts with oxygen forming an unstable deep violet compound which changes in a stable unsoluble yellow peroxide of the formula C6H5CH2MnO—OMnCH2C6 H5. With excess oxygen a polynuclear complex of 3 valent manganese is formed with the composition Mn4O4(OH)4(OCHC6H5)2.The compounds isolated were characterized by the products of hydrolyses and thermolyses, anaerobic reaction with iodine, magnetic moments, i.r. and e.s.r. spectra.
    Notes: Dibenzylmangan-1,4-dioxan reagiert mit Sauerstoff zu einer tiefvioletten instabilen Substanz. Diese wandelt sich in ein stabiles gelbes, schwerlösliches Peroxid der Formel C6H5CH2MnO—OMnCH2C6H5 um. Mit überschüssigem Sauerstoff entsteht daraus ein Mehrkernkomplex des 3wertigen Mangans der Zusammensetzung Mn4O4(OH)4(OCHC6H5)2.Die isolierten Verbindungen wurden durch ihre Hydrolyse- und Thermolyseprodukte, anaerobe Iodierung, magnetischen Momente sowie IR- und ESR-Spektren näher charakterisiert.
    Additional Material: 1 Tab.
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  • 7
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Organo Transition Metal Compounds. 52. Preparation, Characterization, and Reactions of (C5H5)3Ce · THF and Na[Ce(C5H5)4] · THF(C5H5)3 · THF (I) was synthesized in a simple manner by reaction of (NH4)2[Ce(NO3)6] with C5H5Na. With excess C5H5Na the complex Na[Ce(C5H5)4] · THF (II) could be obtained.In addition of cyclovoltammetric and polarographic measurements it was tried without success to transfer I and II into organocerium(IV) compounds by means of different oxidizing agents. II reacts with I2 and (C6H5)3CCl forming Na[(C5H5)3CeI] · THF or Na[(C5H5)2CeI2] · 4 THF and I besides of (C6H5)3CCl respectively. At interaction of I with Co(acac)3 the cobalticinium salt [(C5H5)2Co][C5H5Ce(acac)3] is formed.The compounds obtained were characterized by elementary analysis, hydrolysis products, magnetic moments, i.r., 1H-n.m.r. und u.v.-vis spectra, and measurements of electric conductivity.
    Notes: (C5H5)3 · THF (I) kann auf bequeme Weise durch Umsetzung von (NH4)2[Ce(NO3)6] mit C5H5Na erhalten werden. Bei Verwendung eines Überschusses von C5H5Na entsteht das bisher nicht beschriebene Na[Ce(C5H5)4] · THF (II).Ausgehend von cyclovoltammetrischen und polarographischen Messungen wurden Versuche zur Überführung von I und II in Organocer(IV)-Verbindungen mittels verschiedener Oxydationsmittel angestellt. Diese verliefen negativ im Sinne der Zielstellung. II reagiert mit I2 zu Na[(C5H5)3CeI] · THF bzw. Na[(C5H5)2CeI2]. 4 THF und mit (C6H5)3CCl zu (C5H5)3Ce · THF neben C5H5C(C6H5)3. Bei der Einwirkung von Co(acac)3 auf I entsteht das Cobalticinium-Salz [(C5H5)2Co][C5H5Ce(acac)3].Eine detaillierte Charakterisierung der erhaltenen Verbindungen erfolgte durch ihre Elementaranalysen, Hydrolysenprodukte, magnetischen Momente, IR-, 1H-NMR- und Elektronenspektren sowie durch Leitfähigkeitsmessungen.
    Additional Material: 1 Ill.
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  • 8
    Publication Date: 1984-01-01
    Print ISSN: 0009-5893
    Electronic ISSN: 1612-1112
    Topics: Chemistry and Pharmacology
    Published by Springer
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  • 9
    Publication Date: 1984-09-01
    Print ISSN: 0014-4851
    Electronic ISSN: 1741-2765
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Springer
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  • 10
    Publication Date: 1988-01-01
    Print ISSN: 0016-1152
    Topics: Chemistry and Pharmacology
    Published by Springer
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