M
Michelle L. Coote
Researcher at Australian National University
Publications - 357
Citations - 15471
Michelle L. Coote is an academic researcher from Australian National University. The author has contributed to research in topics: Radical polymerization & Polymerization. The author has an hindex of 62, co-authored 336 publications receiving 13050 citations. Previous affiliations of Michelle L. Coote include Durham University & University of New South Wales.
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Journal ArticleDOI
Electrostatic catalysis of a Diels–Alder reaction
Albert C. Aragonès,Naomi L. Haworth,Nadim Darwish,Simone Ciampi,Nathaniel J. Bloomfield,Gordon G. Wallace,Ismael Díez-Pérez,Michelle L. Coote +7 more
TL;DR: Experimental evidence is provided that the formation of carbon–carbon bonds is accelerated by an electric field, and a fivefold increase in the frequency of formation of single-molecule junctions is found.
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Understanding atom transfer radical polymerization: effect of ligand and initiator structures on the equilibrium constants.
Wei Tang,Yungwan Kwak,Wade A. Braunecker,Nicolay V. Tsarevsky,Michelle L. Coote,Krzysztof Matyjaszewski +5 more
TL;DR: Equilibrium constants in Cu-based atom transfer radical polymerization (ATRP) were determined for a wide range of ligands and initiators in acetonitrile at 22 degrees C and excellent correlations of the equilibrium constants with the Cu(II/I) redox potentials and the carbon-halogen bond dissociation energies were observed.
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Mechanism and kinetics of dithiobenzoate-mediated RAFT polymerization. I. The current situation
Christopher Barner-Kowollik,Michael Buback,Bernadette Charleux,Michelle L. Coote,Marco Drache,Takeshi Fukuda,Atsushi Goto,Bert Klumperman,Andrew B. Lowe,J. B. McLeary,Graeme Moad,Michael J. Monteiro,Ronald D. Sanderson,Matthew P. Tonge,Matthew P. Tonge,Philipp Vana +15 more
TL;DR: In this article, the authors comprehensively reviewed the kinetics and mechanism of dithiobenzoate-mediated Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerizations, which exhibit nonideal kinetic behavior, such as induction periods and rate retardation.
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A universal approach for continuum solvent pK a calculations: are we there yet?
Junming Ho,Michelle L. Coote +1 more
TL;DR: The results indicate that the direct method is unsuitable for general pKa calculations, although moderately accurate results (MAD <3 units) are possible for certain classes of acids, depending on the choice of solvent model.
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Comment on the correct use of continuum solvent models.
TL;DR: There are a growing number of recent studies that employ alternative approaches to evaluating G soln and this comment aims to highlight some of their shortcomings as well as clarify some potential points of confusion concerning the usage of these models.