Abstract

The self-assembly of Cu(I) ions with N-[(E)-(4-chlorophenyl)methylidene]-4H-1,2,4-triazol-4-amine (L1) and various spacer ligands yields five different crystalline species: ∞1{[Cu2(μ-L1)2(μ-L2)(CH3CN)2](ClO4)2} (3) (L2 = pyrazine), ∞1{[Cu(L1)(μ-L3)(CH3CN)](ClO4)} (4) and ∞1{[Cu(L1)2(μ-L3)](ClO4)} (5) (L3 = 4,4′- bipyridyl), ∞3{[Cu2(μ-L1)2(μ-L4)2][Cu(μ-L4)3/2(CH3CN)]2(ClO4)4·6CH3CN} (6) and ∞2{[Cu2(μ-L1)2(μ-L4)3(CH3CN)](ClO4)2·CH3CN} (7) (L4 = 1,4-bis(3-pyridyl)-2,3-diaza-1,3-butadiene). Complexes 3−5 are zigzag polymeric one-dimensional (1D) chains, 7 shows a two-dimensional (2D) layered structure, whereas 6 forms a three-dimensional (3D) polymeric structure. In crystals of 3 and 7, the nodes of the polymers are formed by two copper(I) ions bridged by two N1,N2-coordinated triazole ligands L1. Such a coordination mode was previously observed for dimeric complexes {[Cu2(L1)4](ClO4)2}·2CH3CN (1) and {[Cu2(L1)4(CH3CN)2](ClO4)2}·CH3CN (2), and the {Cu-(μ-L1)2-Cu} fragment can be treated as a secondary buildin...

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