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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 277-280 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetik und Mechanismus der Reduktion von Kobalt(III)-Trisacetylacetonat durch Hydrazin in saurem MediumDie Kinetik der Reduktion von Kobalt(III)-Trisacetylacetonat durch Hydrazin in wäßrig-perchlorsaurer Lösung wurde unter unterschiedlichen Bedingungen untersucht.
    Notes: The kinetics of reduction of tris(acetylacetonato)cobalt(III) by hydrazine in aqueous perchloric acid medium have been studied under different conditions. The complex Co(acac)3 and its protonated form Co(acac)2(acacH+) are both reduced by N2H4 with specific rate constants kR and kH,R respectively. These reactions occur concurrently with the self reduction of the complex in acid media having a specific rate constant kH. From detailed analysis of the effects of acid and hydrazine concentration on the rate, values of kH, kR and kH,R have been determined at 30°, 40° and 50°C at an ionic strength of 2 and from these the corresponding activation parameters ΔH≠ and ΔS≠ have been evaluated. The mechanism appears to involve the formation of intermediates in which N2H62+ is hydrogen bonded to Co(acac)3 and Co(acac)2(acacH+) respectively each of which possibly decomposes (rate determining) by H atom transfer from N2H62+ to the bound acetylacetonate ligand, leading to an electron transfer to cobalt(III) forming cobalt(II).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 223 (1990), S. 107-113 
    ISSN: 1617-4623
    Keywords: Yeast genes ; Inactivation ; Transcription ; Recombination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The LEU2 gene of a his3 strain was inactivated by inserting the HIS3 gene between two overlapping inactive leu2 gene fragments, and mitotic stability of the resulting leu2: HISS: : leu2 sequence was measured under leucine repression and derepression. Both inactive leu2 regions were transcribed under derepressing conditions (growth in low leucine), and the LEU2 gene was completely restored by illegitimate recombination between the overlapping tandem repeats, leading to the loss of the intervening HIS3 gene. In contrast, only the downstream leu2 fragment was transcribed upon leucine repression, and the HIS3 insert in the leu2 region remained intact. The reciprocal experiment (inactivation of the HIS3 gene by inserting the marker gene LEU2) revealed a moderate rate of HIS3 restoration and LEU2 excision, reflecting transcriptional activity of the HIS3 region intermediate between that of LEU2 transcription in the repressed and derepressed state.
    Type of Medium: Electronic Resource
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