Abstract

p-Thioacetatebenzoic acid (H2L) and a combination of N-donor ligands such as 4,4′-bipyridine (4,4′-bipy) and 1,3-bi(4-pyridyl)propane (bpp) with metal ions Mn(II) and Ni(II) give rise to two coordination polymers, namely, [Mn(HL)2(bpp)2(H2O)2] n (1), [NiL (4,4′-bipy)(H2O)3] n ·nH2O (2). 1 features an unusual “8” shaped double layer by hydrogen bonds and two different types of helical chains are arrayed alternatively in the 2D double layer framework, which further extends into a 3D supramolecular structure through C–H···O hydrogen bonds. 2 consists of 1D chains which further connect with each other via hydrogen bonds to form the final 3D framework including two different types of helical structure. Photoluminescence study reveals that 1 displays intense structure-related fluorescent emission bands (λex = 369 nm) at 414 nm in the solid state at room temperature. Electrochemical property of 2 reveals that the process of the redox is irreversible. p-Thioacetatebenzoic acid (H2L) and a combination of N-donor ligands such as 4,4′-bipyridine (4,4′-bipy) and 1,3-bi(4-pyridyl)propane (bpp) with metal ions Mn(II) and Ni(II) give rise to two coordination polymers with two different helices, namely, [Mn(HL)2(bpp)2(H2O)2] n (1), [NiL (4,4′-bipy)(H2O)3] n ·nH2O (2).

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