Abstract

Crystals of La and Ce complexes of water-soluble p-sulfonatothiacalix[6]arenes showed that thiacalixarene molecules adopt a 1,2,3-alternate conformation. In contrast, crystals of Eu, Tb, Tm, Yb, and Lu complexes of p-sulfonatothiacalix[6]arenes indicated that thiacalixarene molecules maintain an ‘up-down’ double partial-cone conformation. In the extended structures of the La and Ce complexes, a one-dimensional ‘ladder-type’ coordination polymer was formed via direct coordination of the sulfonate groups of the thiacalixarene molecules to the aquated metal cations. Three-dimensional supramolecular network assemblies are constructed from the piles of ‘ladder-type’ polymers formed via hydrogen bonds, O⋯O and S⋯S interactions, and S–π interactions. In contrast, the extended structures of the Eu, Tb, Tm, Yb, and Lu complexes form via mutually supporting intermolecular π–π stacking, S–π interactions, and hydrogen-bonding interactions between two differently directed polymers.

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