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  • Organic Chemistry  (6)
  • molecular devices
  • Self-assembly
  • 1985-1989  (6)
  • 1989  (2)
  • 1985  (4)
Collection
Keywords
  • Organic Chemistry  (6)
  • molecular devices
  • Self-assembly
  • Chemistry  (6)
Publisher
Years
  • 1985-1989  (6)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 68 (1985), S. 289-299 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of five macrobicyclic polyamines 1-5 is described following a route in which the macrobicycle is formed by the coupling of two tripodal subunits. Such a sequence is appreciably shorter than the stepwise construction via a macrocycle, and may give higher yields, as illustrated by the case of bis-tren 3, which has been synthesized following both routes.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of the complex [phen · phen · phen] · NaBr · 2 CHCl3 of the macrobicyclic ligand 1 has been determined. The complex is of cryptate type, the Na+ cation being contained in the molecular cavity of 1 and coordinated to all eight N-atoms. The ligand has a propeller shape and interconverts in solution between the two enantiomeric helical forms.
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nature and Stability of Some Metallic Complexes of Dinucleating Cryptands in Solution. I. A Polyazapolyoxa Cylindrical Macrotricycle and its Monocyclic SubunitpH-metry and UV spectrophotometry were used to study the complexing properties of the cylindrical macrotricycle, 1,7,13,19-tetraaza-4,16-dioxa-10,22,27,32-tetraoxatricyclo[17.5.5.5]tetratriacontane (1) and of its constitutive monocyclic subunit, 1,7-diaza-4,10-dioxacyclododecane (2) with some transition and heavy metal cations (Cu2+, Co2+, Ni2+, Zn2+, Cd2+, Pb2+, Ag+), in aqueous medium 0.1M Et4NClO4, at 25°. The protonation constants of the ligands as well as the nature and the stabilities of the complexes formed in the pH-regions studied were determined. The tricycle 1 only formed dinuclear M2L complexes with Cu2+, Zn2+, and Ag+, accompanied in the latter case by a protonated mononuclear MLH species, and with Cu2+ and Zn2+ at high pH-values by dinuclear hydroxo complexes. Only mononuclear complexes were evidenced with the other cations, ML being accompanied either by protonated or hydroxy mononuclear species. The mononuclear complexes of 1, when they existed, were more stable than the corresponding complexes of 2, except for cobalt which formed complexes of comparable stability with both ligands. In the other cases (Cd2+, Pb2+, Ag+), the stability differences between the complexes of 1 and 2 increased with the size of the cation.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nature and Stability of Some Metallic Complexes of Dinucleating Cryptands in Solution II. Polythiamacrotricycles and Related Monocyclic SubunitsThe stability constants of the Cu2+ and Ag+ complexes of the cylindrical macrotricycle 1a (1,7,13,19-tetraaza 4,16-dioxa 10,22,27,32-tetrathiatricyclo[17.5.5.5]tetratriacontane) have been determined by pH-metry, as well as those of the Cu2+, Co2+, Zn2+, Cd2+, Pb2+, and Ag+ complexes of the monocyclic subunit 2a (1,7-dimethyl-1,7-diaza 4,10-dithiacyclododecane), in aqueous solutions (NaClO4) at 25°. In the Cu(II) systems, equilibria were reached slowly, and the results established by pH-metry were confirmed by UV/VIS spectrophotometric studies. The tricycle 1a forms dinuclear cryptates with copper and silver, with overall stability constants log β210 (Cu2-1a)4+ = 18.5, log β21-2 (Cu2-1a(OH)2)2+ = 4.8, log β210(Ag2-1a)2+ = 23.0. Ag+ also forms a mononuclear (Ag-1a)+ complex, with log β110 = 13.1, but no mononuclear species were detected in the Cu-1a system. The absorption spectra of the bis-Cu(II) complexes of 1a and 2a in aqueous medium, MeOH and propylene carbonate (PC) are given, as well as those, in MeOH and PC, of the bis-copper complexes of the related monocycles 3 and 4 (1,7-diaza-4,10,13-trithiacyclopentadecane and 1.10-diaza 4,7,13,16-tetrathiacyclooctadecane, respectively), and tricycle 5 with two benzyl groups in the lateral chains.The complexing properties of the polyoxa- and polythia macrotricycles (Parts I and II of this series) are compared to those of other bis-chelating ligands, the bicyclic bis-tren and the monocyclic bis-dien.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 72 (1989), S. 1066-1077 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of nine macrocyclic polyamines 2-10 containing pyridine units is described. These compounds are 22- (9), 24- (2-4,6,8,10), or 26- (5, 7) membered hexaaza (2,3,9,10) or octaaza (4-7) macrocycles in which one to four pyridine units are incorporated. Compounds 3,4,9, and 10 are homoditopic ligands, whereas 2 and 5 are heteroditopic and 6-8 multitopic receptors. Compounds 2-10 are potential ligands for metal cations as well as, in their protonated forms, for anions. Protonated macrocycles 2-10 are also potential catalysts for the hydrolysis of nucleotides and polyphosphates.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 72 (1989), S. 1078-1083 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Binding of chloride anion by protonated polyamines was investigated by 35Cl—NMR spectroscopy. The presence of protonated macro(poly)cyclic polyamines caused downfield shifts and significant line broadening of the 53Cl—NMR signals. 35Cl—NMR spectroscopy was used for complex-formation stoichiometry determination and revealed the formation of a binuclear chloride complex with the fully protonated ditopic hexaazamacrocyclic receptor 6. 35Cl—NMR spectroscopy was also applied in competition experiments between Cl— and SO42- and demonstrated that the fully protonated macrocyclic hexaamine 4 forms a strong complex with SO4-2 with 1:1 stoichiometry.
    Additional Material: 3 Ill.
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