M
Marc A. Hillmyer
Researcher at University of Minnesota
Publications - 598
Citations - 41267
Marc A. Hillmyer is an academic researcher from University of Minnesota. The author has contributed to research in topics: Copolymer & Polymerization. The author has an hindex of 103, co-authored 574 publications receiving 36643 citations. Previous affiliations of Marc A. Hillmyer include University of Colorado Boulder & University of North Carolina at Chapel Hill.
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Hierarchically porous polymers from hyper-cross-linked block polymer precursors
TL;DR: In this article, a hierarchical porous polymers (HPPs) consisting of micropores and well-defined 3D continuous mesopores was synthesized by combination of hyper-cross-linking and block polymer self-assembly.
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Effects of Polydispersity on the Order-Disorder Transition in Block Copolymer Melts
TL;DR: In this paper, controlled polydispersity poly(ethylene-alt-propylene)-b-poly(DL-lactide) (PL) and polystyrene-b-Polyisoprene (SI) block copolymers were studied to study the effects of the molecular weight distribution on the order-disorder transition at controlled composition and overall molecular weight.
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Synthesis of fluorinated polymers by chemical modification
TL;DR: In this paper, a review of methods for the bulk incorporation of fluorine in or along the backbone of macromolecules with fluorination procedures adhering to these criteria is presented.
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Mechanistic study of the stereoselective polymerization of D, L-lactide using indium(III) halides
Agostino Pietrangelo,Spencer C. Knight,Aalo K. Gupta,Letitia J. Yao,Marc A. Hillmyer,William B. Tolman +5 more
TL;DR: A model system that polymerizes D,L-LA with the same high degree of stereoselectivity was developed using 3-diethylamino-1-propanol in lieu of BnOH and NEt(3), and this system was found to be effective for the polymerization of other cyclic esters, including epsilon-caprolactone and several substituted derivatives.
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Synthesis of Sequence-Specific Vinyl Copolymers by Regioselective ROMP of Multiply Substituted Cyclooctenes
TL;DR: In this article, a variety of multisubstituted cyclooctenes were prepared and employed as monomers for ring-opening metathesis polymerization using the Grubbs second or third generation catalysts.