Cyanide as a bridge can be used to construct homo- and heterometallic complexes with intriguing structures and interesting magnetic properties. These ligands can generate diverse structures, including clusters, one-dimensional chains, two-dimensional layers and three-dimensional frameworks. The title cyanide-bridged Cu(II)-Co(III) heterometallic compound, [Cu(II)Co(III)(CN)6(C4H11N2)(H2O)]n, has been synthesized and characterized by single-crystal X-ray diffraction analysis, magnetic measurement, thermal study, vibrational spectroscopy (FT-IR) and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM-EDS). The crystal structure analysis revealed that it has a two-dimensional grid-like structure built up of [Cu(Hpip)(H2O)](3+) cations (Hpip is piperazinium) and [Co(CN)6](3-) anions that are linked through bridging cyanide ligands. The overall three-dimensional supramolecular network is expanded by a combination of interlayer O-H...N and N-H...O hydrogen bonds involving the coordinated water molecules and the N atoms of the nonbridging cyanide groups and monodentate cationic piperazinium ligands. A magnetic investigation shows that antiferromagnetic interactions exist in the title compound.

Calcium sulfate/tri-calcium phosphate (CaSO4/TCP) composite bone fillers were fabricated through molding method. Their structure and properties were characterized by infrared spectroscope, scanning electronic spectroscope, x-ray diffraction and degradation test. The results show that TCP crystals were attached to the CaSO4 crystals and prevented the growing of sulfate crystals. So their size is shorter than that of CaSO4 crystals prepared from pure CaSO4 semihydrate, and some even had defect. The resorption rate of CaSO4 bone fillers was decreased when TCP was incorporated.

The colloidal crystal template or opal with a closed-packed face centered cubic (fcc) lattice was prepared from monodisperse polystyrene (PS) microspheres by gravity sedimentation, and it was used for the fabrication of polyaniline hybrid with inverse opal structure. The template provided void space for the infiltration of Bi2Te3 and monomer that was then in situ polymerized to polyaniline. The opal composite was then soaked in toluene for completely removing PS microspheres to form porous polyaniline hybrid with inverse opal structure. The PS microspheres were replaced by air microspheres, which interconnected each other through the windows on the polyaniline hybrid wall. Both the wall and the air void constitute continuous phases. The polyaniline hybrid with inverse opal structure was observed with scanning electronic microscopy.