Abstract

The straightforward self-assembly reaction of R3Sn+ and [Fe(CN)6]3− affords three-dimensional (3-D) coordination polymers [(n-Bu3Sn)2(R3Sn)Fe(CN)6] n , R = n-Bu(I) or Ph(II). The architecture of these coordination polymers is closely related to zeolite and acts as a host with wide internal cavities or channels capable of encapsulating voluminous organic compounds. Aniline derivatives acting as guest are encapsulated within the cavities of the 3-D-polymeric hosts I and II by tribochemical reaction producing host–guest supramolecular polymers. The structures and physical properties of these hosts and their host–guest systems were investigated by elemental analysis, X-ray powder diffraction, IR, UV-vis, EPR, and magnetic measurements. The morphology of these systems was examined by scanning electron microscopy (SEM). The interesting feature of these host–guest supramolecular polymers is the enhanced electrical conductivities over those of the 3-D-coordination polymeric hosts upon encapsulation of conductive polymers within their cavities.

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