@article{vargantwar_brannock_tauer_spontak_2013, title={Midblock-sulfonated triblock ionomers derived from a long-chain poly[styrene-b-butadiene-b-styrene] triblock copolymer}, volume={1}, ISSN={["2050-7496"]}, DOI={10.1039/c2ta00022a}, abstractNote={Selective sulfonation of a poly[styrene-b-butadiene-b-styrene] (SBS) triblock copolymer has been performed with a sulfur trioxide–dioxane (SO3–dioxane) complex to generate midblock-sulfonated triblock ionomers possessing varying degrees of sulfonation (DOS). Products of the sulfonation reaction have been characterized by proton nuclear magnetic resonance and Fourier-transform infrared spectroscopies to ensure sulfonation only involves the B midblocks. Due to this targeted sulfonation, the lower glass transition temperature (Tg) disappears completely in all the ionomers examined, indicating that the formation of ionic aggregates restricts the mobility of the B midblocks. Such aggregates hinder microphase separation and promote a diffuse interface, as established by progressive broadening of the upper Tg with increasing DOS. Additional evidence of diffuse interfaces and matrix densification is provided by small-angle X-ray scattering, which reveals a concurrent size reduction in microdomain spacing with increasing DOS. A sulfonation-induced order–order morphological transition from cylinders to lamellae is likewise observed. Due to the retention of microphase-separated glassy microdomains that serve as physical crosslinks, these triblock ionomers are capable of absorbing remarkably high solvent levels and forming highly swollen gel networks in polar media, thereby making them suitable for use in hygiene and healthcare applications, as well as in devices requiring ion transport.}, number={10}, journal={JOURNAL OF MATERIALS CHEMISTRY A}, author={Vargantwar, Pruthesh H. and Brannock, Molly C. and Tauer, Klaus and Spontak, Richard J.}, year={2013}, pages={3430–3439} }
 @article{brannock_behof_morrison_gorman_2011, title={Overcoming challenges in the palladium-catalyzed synthesis of electron deficient ortho-substituted aryl acetonitriles}, volume={9}, ISSN={["1477-0539"]}, DOI={10.1039/c0ob00903b}, abstractNote={Highly electron deficient monoaryl, di-aryl and bis-diaryl acetonitriles were effectively synthesized using either a nucleophilic aromatic substitution (NAS) or a palladium-mediated coupling pathway. Synthesis of di-aryl acetonitriles most conveniently proceeded via NAS--palladium-mediated coupling was not required. This reaction, however, results in a product that is more acidic than the reactants. Facile deprotonation of the product prevents efficient formation of the bis-diaryl acetonitrile through a NAS pathway. Thus, palladium-mediated coupling is required to prepare the bis-diaryl acetonitrile efficiently. In the palladium-catalyzed coupling, choice of base and solvent (and thus the counter cation for the benzylic anion nucleophile) is important. Also, choice of the supporting ligand is important, indicating the sensitivity of the reaction to steric and ligand electronic effects.}, number={8}, journal={ORGANIC & BIOMOLECULAR CHEMISTRY}, author={Brannock, Molly C. and Behof, William J. and Morrison, Gregory and Gorman, Christopher B.}, year={2011}, pages={2661–2666} }