4.7 Article

Topological diversity of coordination polymers containing the rigid terephthalate and a flexible N,N '-type ligand: Interpenetration, polyrotaxane, and polythreading

Journal

CRYSTAL GROWTH & DESIGN
Volume 8, Issue 6, Pages 1932-1939

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cg701232n

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Reactions of zinc(II) or cadmium(II) salts with terephthalic acid (H(2)tp) and 1,3-bis(4-pyridyl) propane (bpp) have afforded four coordination polymers at room temperature, [Zn(mu-tp)(mu-bpp)](n)center dot 2nH(2)O (1), [Cd-2(mu-tp)(2)(mu-bpp)(3)](n)center dot 2nH(2)O (2), [Cd(mu-tp)(mu-bpp)(H2O)](n)center dot nH(2)O (3), and [Cd-2(mu-tp)(mu-bpp)(2)(bpp)(2)Br-2](n) (4). Single-crystal X-ray diffraction has revealed interesting topological features for these compounds. In 1, the Zn atoms act as 4-connected nodes bridged by the tp and bpp ligands to give a 3-fold interpenetrated 3D network with a unique 6(6) topology, which is evidently distinct from 4-connected diamondoid networks. 2 represents the first example of a 2-fold interpenetrated coordination polymer, which possesses a 5-connected 3D framework with a unique 6(10) topology constructed from Cd nodes and tp and bpp spacers. 3 manifests a polyrotaxane motif comprised of two interlocked sets of identical sheets, which result in a 2D -> 2D polythreaded layer. Parallel mutual polythreading of 2D layers with dangling bpp ligands is observed in 4, involving five polymeric layers at a time and thus affording a 3D architecture. All compounds were characterized by infrared spectroscopy, elemental analysis, thermogravi metric analysis, and their fluorescence properties were also investigated.

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