Marc A. Hillmyer

TL;DR: In this article, a process for preparing a polymer composite includes reacting (a) a multi-functional monomer and (b) a block copolymer comprising (i) a first block and (ii) a second block that includes a functional group capable of reacting with the multifunctional monomer, to form a crosslinked, nano-structured, bicontinuous composite.

TL;DR: In this article, a range of well defined μ-A(BC)n "miktobrush" terpolymers were synthesized utilizing the alternating radical copolymerization of two hydrophobic and incompatible macromonomer (MM) building blocks.

TL;DR: In this paper, the authors investigated the dissolution of HPMCAS SDs in phosphate buffered saline (PBS) at loadings of 10, 25, and 50 wt % relative to polymer.

TL;DR: In this paper, primary and secondary amino-functionalized polyethylenes were synthesized from commercially available maleic anhydride-modified polyethylene by reaction with mono-tert-butoxycarbonyl-protected diamines, N-(tertbutoxy carbonyl)-1,6- diaminohexane (tBocHMDA), and N-(TERt)-butoxy-carbonel)-N-ethyl-1, 6-diamino hexane (TBocEtHMDA) followed by deprotec- tion with

TL;DR: This work has developed a strategy involving inexpensive and readily functional vanillin-based monomers to assemble se-quence-defined polyurethane oligomers via sequential reductive amination and carbamation, providing one of the first examples of a scalable synthetic route towards se- quence- defined thermosets that exhibit sequence-dependent properties.