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  • Organic Chemistry  (2)
  • amorphous solid water  (1)
  • Astronomy
  • 1995-1999  (3)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of thermal analysis and calorimetry 52 (1998), S. 109-113 
    ISSN: 1572-8943
    Schlagwort(e): amorphous solid water ; aqueous systems ; DSC ; glass transition ; supercooling
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract After a brief introduction of the terms supercooling, amorphous solid state, glass transition and devitrification, the known ways of production of amorphous solid water are discussed. DSC experiments with quench cooled aqueous solutions show the phenomenon of glass transition and devitrification.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Three N2S2 macrocycles (3, 10, 12) carrying an amino group as a pendant arm have been synthesized and their complexation properties towards Ni2+ and Cu2+ studied. The crystal structures of the Cu2+ complexes with 10-methyl-1,4-dithia-7,10-diazacyclododecane-7-ethanamine (3) and 11-methyl-1,4-dithia-8,11-diazacyclotetradecane-8-ethanamine (10) show that, in both cases, the Cu2+ is pentacoordinated by the four donor atoms of the macrocycle and the amino group of the side chain. In aqueous solution, however, two forms of the complexes with stoichiometries [MLH] and [ML] (M = Cu2+ or Ni2+) have been observed. In [MLH], the amino group is protonated and does not bind to the metal ion, whereas in [ML] the amino group is bound, and a pentacoordinated geometry results. The pKa values for the equilibrium [ML] + H+⇌[MLH]+ decrease in the order 12 〉 10 〉 3, indicating that the 2-aminoethyl side chain binds better to the Cu2+ than the 3-aminopropyl side chain. Cyclic voltammetry for the Cu2+/Cu+ pair shows that the 2-aminoethyl pendant arm stabilizes the Cu2+ oxidation state, when the metal ion is in the 14-membered ring (10), whereas it stabilizes Cu+ for the 12-membered macrocycle (3).
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 1325-1333 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A series of N2S2-macrocycles with ring sizes varying between 12 and 16, as well as two 12-membered N2S2-rings with a pendant carboxylic and amino group, respectively, were synthesized. Their complexation properties towards Ag+ were studied by pH titrations and by potentiometry with a silver electrode. The observation that 1:1 ([AgLH2]3+, [AgLH]2+, [AgL]+) and 1:2 species ([AgL2H2]3+, [AgL2H]2+, [AgL2]+) were formed is interpreted by postulating that Ag+ can bind either to the S-donors only, or to both the N- and S-atoms. The most stable complex [AgL]+ in the series of the nonfunctionalized macrocycles was found for the 12-membered N2S2-ring 3. The stability of it increased when an additional donor group was introduced into the side chain. The highest formation constant (logβ110 = 14.43(1)) was obtained with the 12-membered ring 12 carrying the ethanamine side chain. In view of a radiochemical application, all Ag+ complexes were tested in blood serum for their stability, but were not stable enough against transmetallation.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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