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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Molecular tectonics: P-H-thiacalix4arene pyridyl appended positional isomers as tectons for the formation of 1D and 2D mercury coordination networks
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Molecular tectonics: P-H-thiacalix4arene pyridyl appended positional isomers as tectons for the formation of 1D and 2D mercury coordination networks

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Three p-H-thiacalix4arene pyridyl appended coordinating tectons (2-4) in a 1,3-alternate conformation have been prepared and structurally characterised in the solid state. These compounds are positional isomers differing only by the position of the nitrogen atom on the pyridyl ring. Their combinations with HgCl_2 lead to the formation of 1- and 2-D neutral mercury coordination networks. Whereas for tecton 2 (ortho isomer) a 2D architecture resulting from the bridging of consecutive tectons by the mononuclear HgCl _2 unit is obtained, for tecton 3 (meta isomer) again a 2D network is formed. However, in that case, the interconnection of consecutive organic tectons 3 takes place through a binuclear Hg_2Cl_4 species. Finally, in the case of tecton 4 (para position), a 1D ribbon type double chain arrangement resulting from the bridging of consecutive tectons by trinuclear Hg_3Cl_6 units followed by the interconnection of two chains through the fusion of the trinuclear centres into a hexanuclear node is observed. This journal is

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