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  • 1
    Publication Date: 2020-07-27
    Description: In the colloidal synthesis of iron sulfides, a series of dialkyl disulfides, alkyl thiols, and dialkyl disulfides (allyl, benzyl, tert-butyl, and phenyl) were employed as sulfur sources. Their reactivity was found to tune the phase between pyrite (FeS2), greigite (Fe3S4), and pyrrhotite (Fe7S8). DFT was used to show that sulfur-rich phases were favored when the C–S bond strength was low in the organosulfurs, yet temperature dependent studies and other observations indicated the reasons for phase selectivity were more nuanced; the different precursors decomposed through different reaction mechanisms, some involving the oleylamine solvent. The formation of pyrite from diallyl disulfide was carefully studied as it was the only precursor to yield FeS2. Raman spectroscopy indicated that FeS2 forms directly without an FeS intermediate, unlike most synthetic procedures to pyrite. Diallyl disulfide releases persulfide (S–S)2– due to the lower C–S bond strength relative to the S–S bond strength, as well as facile decomposition in the presence of amines through SN2′ mechanisms at elevated temperatures.
    Type: Article , PeerReviewed
    Format: text
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of plant pathology 106 (2000), S. 67-75 
    ISSN: 1573-8469
    Keywords: genetic marker ; PCR-RFLP ; Phoma exigua var. foveata ; polymerase chain reaction ; potato gangrene ; random amplified polymorphic DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Phoma foveata and P. exigua variety exigua both infect potatoes and are morphologically very similar. P. foveata produces a pigment which allows differentiation from P. exigua in culture. Discrimination of the two species based on the production of a secondary metabolite, which is dependent on the growth conditions, is not reliable. Therefore, there is a need to develop nucleic acid based identification markers. A 482 bp random amplified polymorphic DNA (RAPD) fragment from P. foveata was isolated and sequenced. Polymerase chain reaction (PCR) primers, developed from the sequence of the RAPD product, amplified a 474 bp fragment for P. foveata and P. exigua varieties exigua, diversispora, inoxydibilis and sambuci-nigrae. The similarity of the PCR fragments was demonstrated by sequence analysis and by using the restriction enzymes DdeI and DpnII. P. foveata was distinguished from the four varieties of P. exigua on the basis of the RFLP patterns of the PCR fragment. Ten isolates of P. foveata and nine of P. exigua var. exigua from different geographic locations were tested and all isolates but one showed the restriction digest pattern of the PCR fragment (PCR-RFLP) specific to each species. One isolate of P. foveata demonstrated a PCR-RFLP pattern similar to P. exigua var. exigua leading to the conclusion that the isolate had been previously misidentified as a strain of P. foveata lacking the ability to produce pigment.
    Type of Medium: Electronic Resource
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