The design, synthesis and characterization of novel conjugated polymers are described. Using a coupling reaction recently developed within our labs, polymers were constructed through triazene linkages generated by joining N-heterocyclic carbenes (NHCs) with organic azides. This triazene reaction produced polymer of sufficiently high molecular weight as to be spin-coated and rendered conductive upon doping with iodine. The reaction also has potential for executing post-polymerization modifications. This was evidenced through rapid functionalization of poly(4-methylazido-styrene) via triazene formation using a commercially available N-heterocyclic carbene (NHC). A formal anion metathesis of benzobis(imidazolium)s was used to transform neutral block copolymers into block ionomers. Further investigation of the block ionomers revealed their solvent mediated self assembly. The gradual change of organic to aqueous media caused the adoption of a three-dimensional micelle conformation as determined by transmission electron microscopy and dynamic light scattering. Through the exploitation of carbene-carbon disulfide adducts, new chain transfer agents were generated. After 2-dithiocarboxylate-imidazolium adduct formation, alkylation was performed with benzyl bromide. The resulting charged chain transfer agent was tested for its ability to moderate radical addition fragmentation (RAFT) polymerizations of styrene. A considerable increase in transfer kinetics as compared to that of commonly used RAFT agents was observed whilst retaining low polydispersity and molecular weight control. The rate enhancement is presumably due to the electron withdrawing imidazolium activating the thionyl towards the nucleophilic radical while retaining effective fragmentation. Ion coordinating macrocycles were affixed to a poly(methacrylate) scaffold for employment as electrolyte extractants. Polymer bound calix[4]pyrrole was found to complex fluoride and chloride with sufficient strength as to extract tetrabutylammonium salts from water. Enhanced extraction abilities were observed when calix[4]pyrrole was used in conjunction with benzo-15-crown-5. Methacrylate polymers containing both macrocycles affected the removal of aqueous potassium fluoride from a biphasic water/dichloromethane mixture. To provide evidence for the presence of potassium fluoride within the dichloromethane layer, ¹⁹F NMR and flame emission spectroscopy were used. / text

The covalent bond formed between a N-heterocyclic carbene and an aryl-isothiocyanate was discovered to be thermally-reversible. This bond was incorporated into the backbone of an aromatic polymer which, when subjected to heat and excess monomer, would depolymerize to smaller oligomers. In addition these small molecules contain active chain ends and could be repolymerized to reform the original polymer. The high molecular weight material was made into freestanding sheets with desirable mechanical properties and could be made conductive by treatment with iodine. A new poly(triazene) was formed from the reaction of a facially opposed, annulated, bis-N-heterocyclic carbene (NHC) and an organic bis-azide. The NHC as well as the azide were varied and combined to produce a series of polymers which were characterized by GPC, TGA, and NMR. These thermally robust polymers were also coated onto glass slides and rendered electrically conductive by exposure to iodine vapor. A new reagent for Reversible Addition Fragmentation Chain Transfer Polymerization (RAFT) is described. This imidazolium based reagent shows unusually fast kinetics which allows it to control polymerizations at significantly reduced loadings compared to the more traditional neutral dithiocarbamates or dithioesters. The fast kinetics is explained by the rapid rotation of the dithioester about the plane of the cationic N-heterocycle. Sulfonated poly(ether ether ketone) (sPEEK) membranes were blended with imidazoles with varying pKas. The proton conductivity of the membranes was evaluated as a function of pKa and temperature. Interestingly, the conductivity of the dry membranes showed a non-monotonous profile over a temperature range of 25 – 150 C. We use a theoretical model to better understand the mechanistic origins of the observed temperature–conductivity profiles. This model is based on the reaction equilibria between sPEEK’s sulfonic acid groups and the basic sites of the added heterocycles. Using the copper-catalyzed 1,3-dipolar “click” cycloaddition reaction, poly(sulfone)s containing pendant azide moieties were functionalized with various amounts of sodium 3-(prop-2-ynyloxy)propane-1-sulfonate and crosslinked with 1,7-octadiyne. The degree of sulfonation as well as the degree of cross-linking was systematically varied by changing the ratios of the aforementioned reagents. The polymers were cast into membranes, acidified, and then tested for proton conductivity, methanol permeability, and membrane-electrode assembly (MEA) performance. / text