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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Genetic resources and crop evolution 44 (1997), S. 491-493 
    ISSN: 1573-5109
    Keywords: Allium ; cultivar ; genetics ; germplasm ; registration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Genetic lines and example cultivars are used as markers to define variation when describing or evaluating wild or cultivated germplasm. Occasionally genotypes previously described in the literature are no longer available. This was thought to be the case for chartreuse skin colour in Onion. However, registration authorities undertaking Distinctness, Uniformity and Stability tests recently observed this skin colour in the cultivar Greenella and have provided seed to a genebank for long-term conservation. This characteristic is suitable both for use as a genetic marker and as an example cultivar for describing Onion skin colours.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 39 (1956), S. 722-728 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex formation of cis- and trans-1,2-Diaminocyclohexan with the ions H+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+ has been studied. The metal complexes of the trans-diamine are slightly more stable than the corresponding complexes of ethylenediamine, which is probably due to a somewhat more positive entropy term of the formation reaction. The complexes of the cis-compound are somewhat less stable than those of the trans-diamine. The distance between the two basic nitrogen atoms are almost certainly the same in both diamine molecules. The cis-compound, however, has a less favourable geometry for complex formation, because the chelate ring and the 6-membered carbon ring do not lie in the same plane as will be the case with the complexes of the trans-diamine.
    Additional Material: 2 Ill.
    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 45 (1962), S. 775-783 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From a solution containing a mercury(II)salt and thiocyanate (ratio of about 1:4), a solution of a cobalt(II) salt precipitates, in presence of benzene, a bright pink mikrocrystalline compound of the exact composition: {CoHg2(SCN)6, C6H6}, which can be also obtained in well developed cristals. Reflexion and IR. Spectra show that CoII is octahedrally coordinated and that all six thiocyanate groups serve to bridge the two metal atoms: Hg…SCN…Co. It is suggested that the molecule of benzene formes π-bonds simultaneously with two mercury atoms, being the fourth ligand of each Hg2+. Benzene can be replaced by toluene, the three xylenes, naphthalene, anthracene, but not by aliphatic cyclic hydrocarbons. CoII can be replaced by octahedral NiII and CdII, but not by ZnII and CuII. The compounds are thermodynamically unstable. At about 100°C the cobalt-benzene compound loses the hydrocarbon rapidly and the colour of the solid residue turns from pink to a brilliant blue, due to the formation of a 1:1 mixture of {CoHg(SCN)4} and {Hg(SCN)2}. The compound {CoHg2(SCN)6} is non-existent, and it is unlikely therefore that it can serve as a host-lattice for benzene in a clathrate.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 29 (1884), S. 489-493 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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