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Michael S. Hill

Researcher at University of Bath

Publications -  244
Citations -  10123

Michael S. Hill is an academic researcher from University of Bath. The author has contributed to research in topics: Catalysis & Magnesium. The author has an hindex of 52, co-authored 234 publications receiving 8870 citations. Previous affiliations of Michael S. Hill include University of Kentucky & Quaid-i-Azam University.

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Alkaline earths as main group reagents in molecular catalysis.

TL;DR: This review focusses on the developing state of the art in both multiple bond heterofunctionalisation and cross coupling catalysis in alkene and alkyne hydroamination and hydrophosphination catalysis and related extensions of this reactivity that allow the synthesis of a wide variety of acyclic and heterocyclic small molecules.
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Calcium-Mediated Intramolecular Hydroamination Catalysis

TL;DR: The calcium-catalyzed intramolecular hydroamination of alkenes and alkynes is reported and affects catalytic cyclization of a range of aminoalkenes and aminoalkynes with activities that are broadly commensurate to those of established rare earth catalysts.
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Intramolecular hydroamination of aminoalkenes by calcium and magnesium complexes: a synthetic and mechanistic study.

TL;DR: Kinetic analysis of the nonreversible magnesium system revealed that the reaction rate depends directly upon catalyst concentration and inversely upon substrate concentration, suggesting that substrate-inhibited alkene insertion is rate-determining.
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Heterofunctionalization catalysis with organometallic complexes of calcium, strontium and barium

TL;DR: Despite the routine employment of Grignard reagents and Hauser bases as stoichiometric carbanion reagents in organic and inorganic synthesis, a defined reaction chemistry encompassing the heavier e...
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Nanostructured Hybrid Polymer−Inorganic Solar Cell Active Layers Formed by Controllable in Situ Growth of Semiconducting Sulfide Networks

TL;DR: This paper introduces a general method for the fabrication of metal sulfide nanoparticle/polymer films employing a low-cost and low temperature route compatible with large-scale device manufacturing, based upon the controlled in situ thermal decomposition of a solution processable metal xanthate precursor complex in a semiconducting polymer film.