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Michael G. B. Drew

Researcher at University of Reading

Publications -  78
Citations -  1491

Michael G. B. Drew is an academic researcher from University of Reading. The author has contributed to research in topics: Cycloaddition & Aryl. The author has an hindex of 20, co-authored 78 publications receiving 1444 citations. Previous affiliations of Michael G. B. Drew include Instituto Superior Técnico & Indian Institute of Chemical Biology.

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Anion Selective Recognition and Sensing by Novel Macrocyclic Transition Metal Receptor Systems. 1H NMR, Electrochemical, and Photophysical Investigations

TL;DR: A series of novel redox-active and photoactive ruthenium(II) and osmium (II) bipyridyl-, ferrocene-, and cobaltocenium-containing macrocyclic receptors with the dual capability of selectively sensing anionic guest species via electrochemical and optical methodologies have been prepared as discussed by the authors.
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Anion-templated assembly of pseudorotaxanes: importance of anion template, strength of ion-pair thread association, and macrocycle ring size.

TL;DR: Extensive solution 1H NMR binding studies, thermodynamic investigations, and single-crystal X-ray structure determinations reveal that the nature of the halide anion template, strength of the ion-pairing between the anions and the cationic threading component, and to a lesser extent favorable second sphere pi-pi aromatic stacking interactions between the positively chargedthreading component and macrocyclic ligand, affect the efficacy of pseudorotaxane formation.
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Molybdenum η3-Allyl Dicarbonyl Complexes as a New Class of Precursors for Highly Reactive Epoxidation Catalysts with tert-Butyl Hydroperoxide

TL;DR: In this paper, an equatorial−axial arrangement of the bidentate ligand (axial isomer), in contrast with the precursors, found as the equatorial isomer in the solid and fluxional in solution, was used for the catalytic epoxidation of cyclooctene using tert-butyl hydroperoxide as oxidant.
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New Ionophoric Calix[4]diquinones: Coordination Chemistry, Electrochemistry, and X-ray Crystal Structures.

TL;DR: The reduction potentials of the group 1 or 2 metal, ammonium, and alkylammonium complexes are significantly anodically shifted with respect to that of the free ligand and the electrochemical properties of the "acyclic" p-tert-butylcalixdiquinones 1, 4, and 8 and their complexes have been studied using cyclic and square wave voltammetric techniques.
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Calix[4]arene cryptand and new 1,3-bis-pyridyl,-bipyridyl and -alkylthioether calix[4]arenes designed to coordinate transition metal cations

TL;DR: In this article, the syntheses and preliminary transition metal coordination studies of a novel calix[4]arene cryptand receptor and new 1,3-bis-pyridyl-, -bipyrideyl- and -alkylthioether calix are described.