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  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e255-e256 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The X-ray structure determinations of the two title compounds, namely 7-methyl-7,17-diaza-3,11-diazoniabicyclo[11.3.1]heptadeca-1(17),13,15-triene dichloride monohydrate, C14H26N42+·2Cl−·H2O, (I), and 7-methyl-17-aza-3,7,11-triazoniabicyclo[11.3.1]heptadeca-1(17),13,15-triene 2.826-chloride 0.174-nitrate, C14H27N43+·2.826Cl−·0.174NO3−, (II), are reported. Protonation occurs at the secondary amine N atoms in (I) and at all three amine N atoms in (II) to which the Cl− ions are linked via N—H...Cl hydrogen bonds. The macrocyclic hole is quite different in both structures, as is observed by comparing particularly the N3...N4 distances [2.976 (4) and 4.175 (4) Å for (I) and (II), respectively]. In (II), a Cl− ion alternates with an NO3− ion in a disordered structure.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1111
    Keywords: lanthanide(III) complexes ; Schiff-base ; oxaazamacrocycle ; ion selectivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The interaction of lanthanide(III) ions with two N3O3-macrocycles, L1 and L2, derived from 2,6-bis(2-formylphenoxymethyl)pyridine and 1,2-diaminoethane has been investigated. Schiff-base macrocyclic lanthanide(III) complexes LnL1(NO3)3 · xH2O (Ln = Nd, Sm, Eu or Lu) have been prepared by direct reaction of L1 and the appropriate hydrated lanthanide nitrate. The direct reaction between the diamine macrocycle L2 and the hydrated lanthanide(III) nitrates yields complexes LnL2(NO3)3· H2O only for Ln = Dy or Lu. The reduction of the Schiff-base macrocycle decreases the complexation capacity of the ligand towards the Ln(III) ions. The complexes have been characterised by elemental analysis, molar conductivity data, FAB mass spectrometry, IR and, in the case of the lutetium complexes, 1H NMR spectroscopy.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-1948
    Keywords: Metal complexes ; Template synthesis ; Schiff bases ; Oxaazamacrocycles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New series of macrocyclic Schiff-base lanthanide(III), yttrium(III), and cadmium(II) complexes, [M(1)]Xn (X = NO3-, M = Y, Ln = La-Yb except Pm and Dy; X = ClO4-, M = Cd, La, Ce, Pr, Sm, Gd, or Er) and [M(3)]Xn (X = NO3-, M = Dy; X = ClO4-, M = Er and Cd), have been prepared by cyclocondensation of O1,O7-bis(2-formylphenyl)-1,4,7-trioxaheptane with O1,O7-bis(2-aninyl)-1,4,7-trioxaheptane (1) or tris(2-aminoethyl)amine (3) in the presence of the appropriate metal salt as a template agent. The Schiff-base macrocycles 1 and 3 are also formed in the absence of a metal ion. Treatment of 1 with NaBH4 in methanol gives the diamine macrocycle 2. The reactions of LnIII, CdII, and YIII ions with 2 have also been investigated. The crystal structures of the monoprotonated ligand 2 and of the complex [Cd(3)](ClO4)2 have been determined by X-ray diffraction analysis.Supporting information for this article is available on the WWW under -//_/_http://www.wiley-vch.de/contents/jc_2005/2000/99352_s.pdf or from the author.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 1843-1846 
    ISSN: 1434-193X
    Keywords: N-formylation ; Cyclocondensation ; Oxaazamacrocycle ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-formylation of a secondary aliphatic amine has been achieved through the in situ reaction of potassium o-nitrophenolate, generated from o-nitrophenol, K2CO3, KOH, and bis(2-chloroethyl)amine hydrochloride in hot DMF. The initial product, N,N-bis[2-(2-nitrophenoxy)ethyl]formamide has been reduced to provide N,N-bis[2-(2-aminophenoxy)ethyl]formamide which after an MnII-templated cyclocondensation reaction with 2,6-diformylpyridine followed by reductive demetallation with NaBH4 gives an N,N′-diformylated 36-membered N8O4 oxaazamacrocycle.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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