We describe the preparation of nanostructured polymeric materials by polymerizing a monomer within a scaffold composed of self-assembled nanofibrils. 1,3:2,4-Dibenzylidene sorbitol (DBS) is an inexpensive sugar derivative that can form nanofibrillar networks in a variety of organic solvents at relatively low concentrations. Here, we induce DBS nanofibrils in styrene and then thermally initiate the free-radical polymerization of the monomer. The polymerization proceeds without any evidence of macroscopic phase separation, ultimately yielding a transparent solid of polystyrene. Within this material, intact DBS nanofibrils (diameter 10-100 nm) are preserved, as shown by atomic force microscopy (AFM). The DBS fibrils can also be subsequently extracted from the polymer, leaving behind a network of nanoscale pores. The porosity of the resulting polymer has been characterized by the BET technique.

We propose a new method for preparing polymeric nanocomposites and porous materials using self-assembled templates formed by 1,3:2,4-dibenzylidene sorbitol (DBS) organogels. DBS is capable of self-assembling into a 3D nanofibrillar network at relatively low concentrations in some organic solvents to produce organogels. In this study, we induced the formation of such physical cross-linked networks in styrene. Subsequently, we polymerized the styrene in the presence of chemical cross-linkers, divinyl benzene (DVB), with different amounts of DBS using thermal-initiated polymerization. The resulting materials were transparent, homogeneous polystyrene (PS) nanocomposites with both physical and chemical cross-links. The porous polymeric materials were obtained by solvent extraction of the DBS nanofibrils from the PS. Brunauer-Emmett-Teller (BET) measurements show that the amounts of DBS and DVB influenced the specific surface area after the removal of the DBS fibrils.