Electroluminescent networks via photo "click" chemistry.

The use of thiol-ene click chemistry is demonstrated for the first time as a suitable method for cross-linking thin films of 4-phenylethenyl end-capped poly(fluorene). Cross-linking was accomplished by a simple, brief UV curing step at modest temperatures. This chemistry provides an advantage over similar schemes employed for cross-linking conjugated polymers since it does not require elevated temperature or produce potentially detrimental side products. Thiol-ene cross-linking was found to preserve the emissive color integrity of the poly(fluorene) films and allowed for facile photopatterning of the active polymer layer. Furthermore, the investigated cross-linking chemistry was shown to be fully compatible with fabrication of polymer light-emitting diodes (PLEDs) whose performance was comparable to noncross-linked devices. Multicolor PLEDs were also demonstrated by taking advantage of the photopatternability of the thiol-ene based system.

Comparison of facially amphiphilic versus segregated monomers in the design of antibacterial copolymers.

A direct comparison of two strategies for designing antimicrobial polymers is presented. Previously, we published several reports on the use of facially amphiphilic (FA) monomers which led to polynorbornenes with excellent antimicrobial activities and selectivities. Our polymers obtained by copolymerization of structurally similar segregated monomers, in which cationic and non-polar moieties reside on separate repeat units, led to polymers with less pronounced activities. A wide range of polymer amphiphilicities was surveyed by pairing a cationic oxanorbornene with eleven different non-polar monomers and varying the comonomer feed ratios. Their properties were tested using antimicrobial assays and copolymers possessing intermediate hydrophobicities were the most active. Polymer-induced leakage of dye-filled liposomes and microscopy of polymer-treated bacteria support a membrane-based mode of action. From these results there appears to be profound differences in how a polymer made from FA monomers interacts with the phospholipid bilayer compared with copolymers from segregated monomers. We conclude that a well-defined spatial relationship of the whole polymer is crucial to obtain synthetic mimics of antimicrobial peptides (SMAMPs): charged and non-polar moieties need to be balanced locally, for example, at the monomer level, and not just globally. We advocate the use of FA monomers for better control of biological properties. It is expected that this principle will be usefully applied to other backbones such as the polyacrylates, polystyrenes, and non-natural polyamides.