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Jerome R. Robinson

Researcher at Brown University

Publications -  46
Citations -  843

Jerome R. Robinson is an academic researcher from Brown University. The author has contributed to research in topics: Ligand & Catalysis. The author has an hindex of 14, co-authored 36 publications receiving 663 citations. Previous affiliations of Jerome R. Robinson include Texas A&M University System & Wilmington University.

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The electrochemical behavior of cerium(III/IV) complexes: Thermodynamics, kinetics and applications in synthesis

TL;DR: In this paper, the authors survey the general thermodynamic and kinetic characteristics and reported potentials for molecular cerium redox chemistry, and illustrate the ligand types that most effectively stabilize each oxidation state.
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NiXantphos: a deprotonatable ligand for room-temperature palladium-catalyzed cross-couplings of aryl chlorides

TL;DR: Surprisingly, comparison of an extensive array of ligands revealed that under the basic reaction conditions the resultant heterobimetallic Pd–NiXantphos catalyst system outperformed all the other mono- and bidentate ligands in a deprotonative cross-coupling process (DCCP) with aryl chlorides.
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Tuning reactivity and electronic properties through ligand reorganization within a cerium heterobimetallic framework.

TL;DR: An alternative approach has been realized using a rare earth/alkali metal/1,1'-BINOLate (REMB) heterobimetallic framework, which uses redox-inactive metals within the secondary coordination sphere to control ligand reorganization.
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Air- and water-tolerant rare earth guanidinium BINOLate complexes as practical precatalysts in multifunctional asymmetric catalysis.

TL;DR: Self-assembly of novel hydrogen-bonded rare earth metal BINOLate complexes that serve as bench-stable precatalysts for Shibasaki's REMB catalysts, where it is demonstrated that the system performs with comparable or improved levels of stereoselectivity in several mechanistically diverse reactions including Michael additions, aza-Michael additions, and direct Aldol reactions.