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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 31 (1992), S. 1220-1223 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The template reaction of {bis[(S)-2-(aminomethyl)pyrrolidine]}copper(II) with formaldehyde, nitroethane, and base in MeOH yields optically pure {1,7-bis[(S)-pyrrolidin-2-yl]-4-methyl-4-nitro-2,6-diazaheptane}- copper(II) ([Cu((S,S)-mnppm)]2+) in high yield. The same reaction with rac-2-(aminomethyl)pyrrolidine is also described. Preparative details and spectroscopic and electrochemical properties of the CuII complexes and of the free ligands are reported and compared with structural, spectroscopic and electrochemical data of the CuII complex of the unsubstituted parent ligand 1,7-bis[(S)-pyrrolidin-2-yl]-2,6-diazaheptane (ppm). The crystal structure of [Cu(ppm)]Cl ClO4 has been determined by X-ray diffraction methods.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 2041-2049 
    ISSN: 1434-1948
    Keywords: Metal ion selectivity ; Stability constants ; Molecular mechanics ; Metal ion extraction ; Liquid membranes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The syntheses of N,N′-bis-[(2-pyridylmethyl)]-1,3-diamidopropane (papH2) and N,N′-bis-[(2-pyridylmethyl)]-1,3-diamido-2-hexadecylpropane (C16papH2) are reported together with the results of potentiometric titrations of papH2 with Co(II), Ni(II), Cu(II) and Zn(II), spectroscopic and electrochemical data of [Ni(pap)] and [Cu(pap)], structural studies involving the X-ray analyses of the metal-free papH2 ligand and the corresponding Ni(II) and Cu(II) complexes [Ni(pap)] × 2 H2O and [Cu(pap)] × 3 H2O, and force-field calculations (MM) of [Co(pap)], [Ni(pap)], [Cu(pap)] and [Zn(pap)] and the corresponding complexes of the ligand with ortho-methyl-substituted pyridyl groups (Me2papH2); the results of metal ion transport [Co(II), Ni(II), Cu(II) and Fe(II)] from aqueous solutions through C16papH2 containing dichloromethane phases are also given. The extractability with C16papH2 increases along the series Fe(II) 〈 Co(II) 〈 Ni(II) 〈 Cu(II), and this is confirmed by the potentiometric data (papH2, aqueous solutions; logβML[Co(II)] = 1.75; logβMLH-2[Ni(II)] = -11.49; logβML[Cu(II)] = 3.41; logβMLH-2[Cu(II)] = -4.491;logβML[Zn(II)] = 1.87). The structural data (X-ray and MM) indicate that, due to the ortho protons of the pyridyl groups and in dependence of the electronic configuration of the metal center, there is a considerable tetrahedral twist of the central MN4 chromophores {square planar: θ = 0°; tetrahedral: θ = 90°; [Co(pap)]: θ = 15° (MM); [Ni(pap)]: θ = 16° (X-ray), 16° (MM); [Cu(pap)]: θ = 18° (X-ray), 18° (MM); [Zn(pap)]: θ = 23° (MM)}, and this may be enhanced by ortho-methyl substitution of the pyridyl donors {[Co(Me2pap)]: θ = 20° (MM); [Ni(Me2pap)]: θ = 20° (MM); [Cu(Me2pap)]: θ = 24° (MM); [Zn(Me2pap)]: θ = 31° (MM)}, and thus possibly a decrease in the complex stability of Cu(II) and Ni(II) in favor of Zn(II).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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