With controlled nanometre-sized pores and surface areas of thousands of square metres per gram, metal-organic frameworks (MOFs) may have an integral role in future catalysis, filtration and sensing applications. In general, for MOF-based device fabrication, well-organized or patterned MOF growth is required, and thus conventional synthetic routes are not suitable. Moreover, to expand their applicability, the introduction of additional functionality into MOFs is desirable. Here, we explore the use of nanostructured poly-hydrate zinc phosphate (α-hopeite) microparticles as nucleation seeds for MOFs that simultaneously address all these issues. Affording spatial control of nucleation and significantly accelerating MOF growth, these α-hopeite microparticles are found to act as nucleation agents both in solution and on solid surfaces. In addition, the introduction of functional nanoparticles (metallic, semiconducting, polymeric) into these nucleating seeds translates directly to the fabrication of functional MOFs suitable for molecular size-selective applications.

Copper phthalocyanine (CuPc) thin films have been deposited by a recently developed plasma-based method named glow-discharge-induced sublimation (GDS). The deposition of CuPc films has also been obtained by vacuum evaporation (VE) and the comparison of the two methods shows important structural differences. FT-IR and ion beam analyses (RBS-ERDA) show that the GDS-deposited films mainly consist of integer CuPc molecules, but at increasing deposition time the incorporation of damaged molecules becomes important. X-ray diffraction, FT-IR spectroscopy, and UV−vis analysis are used to study the microstructure of the CuPc films and point out that while the VE films consist of only α crystallites, a more disordered structure with the presence of both α and β polymorphs characterizes the GDS films. The latter films are also much more porous as shown by nitrogen physisorption measurements and SEM. Thermal treatments of the GDS films determine a decrease of the structural disorder at 250 °C and the complete transformation to the β polymorph at 290 °C.