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  • Organic Chemistry  (2)
  • Astronomy
  • 1995-1999  (2)
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  • 1
    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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  • 2
    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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