Theory and practice of uncommon molecular electronic configurationsPeptidomimetic Star Polymers for Targeting Biological Ion ChannelsThe effect of leaving radical on the formation of tetrahydroselenophene by SHi ring closure: an experimental and computational study.Design of Redox/Radical Sensing Molecules via Nitrile Imine-Mediated Tetrazole-ene Cycloaddition (NITEC).Maternal depression is associated with DNA methylation changes in cord blood T lymphocytes and adult hippocampiEvaluation of a chiral cubane-based Schiff base ligand in asymmetric catalysis reactions.Computational electrochemistry: prediction of liquid-phase reduction potentials.Bias-Free Chemically Diverse Test Sets from Machine Learning.Hydrophobic Shielding Drives Catalysis of Hydride Transfer in a Family of F420H2-Dependent Enzymes.Molecular dynamics-driven drug discovery: leaping forward with confidence.First determination of the rate constant for ring-closure of an azahexenoyl radical: 6-aza-7-ethyl-5-hexenoyl.Computational study of the chemistry of 3-phenylpropyl radicals.Chloroform as a hydrogen atom donor in Barton reductive decarboxylation reactions.Ab initio evaluation of the thermodynamic and electrochemical properties of alkyl halides and radicals and their mechanistic implications for atom transfer radical polymerization.Suicide inactivation of dioldehydratase by glycolaldehyde and chloroacetaldehyde: an examination of the reaction mechanism.Consistent experimental and theoretical evidence for long-lived intermediate radicals in living free radical polymerization.New insights into 1,2,4-trioxolane stability and the crucial role of ozone in promoting polymer degradation.Experimental and theoretical studies of redox reactions of o-chloranil in aqueous solution.Revealing model dependencies in "Assessing the RAFT equilibrium constant via model systems: an EPR study".Oxidation of 4-substituted TEMPO derivatives reveals modifications at the 1- and 4-positions.Wavelength Dependence of Light-Induced Cycloadditions.Computational design of pH-switchable control agents for nitroxide mediated polymerization.Modeling Flexible Molecules in Solution: A pKa Case Study.Effect of Substituents on the Stability of Sulfur-Centered Radicals.Mechanistic insights into ozone-initiated oxidative degradation of saturated hydrocarbons and polymers.Why are sec-alkylperoxyl bimolecular self-reactions orders of magnitude faster than the analogous reactions of tert-alkylperoxyls? The unanticipated role of CH hydrogen bond donation.Electrostatic catalysis of a Diels-Alder reaction.Protonated alcohols are examples of complete charge-shift bonds.Insights into the hydrogen-abstraction reactions of diol dehydratase: relevance to the catalytic mechanism and suicide inactivation.Origin and scope of long-range stabilizing interactions and associated SOMO-HOMO conversion in distonic radical anions.Should contemporary density functional theory methods be used to study the thermodynamics of radical reactions?Reproducible flaws unveil electrostatic aspects of semiconductor electrochemistry.Mechanisms and energetics of potassium channel block by local anesthetics and antifungal agents.Revising the mechanism of polymer autooxidation.Mechanical Stretching-Induced Electron-Transfer Reactions and Conductance Switching in Single Molecules.Electrochemical and Electrostatic Cleavage of Alkoxyamines.Reversible cyclopropane ring-cleavage reactions within etheno-bridged [4.3.1]propelladiene frameworks leading to aza- and oxa-[5.6.5.6]fenestratetraenes.Can electrostatic catalysis of Diels-Alder reactions be harnessed with pH-switchable charged functional groups?Establishing the True Structure of the Sorbicillinoid-Derived Isolate Rezishanone C by Total Synthesis.Capturing snapshots of post-synthetic metallation chemistry in metal-organic frameworks.
P50
Q28080977-D54EB100-1DB7-4943-B48A-4E42F094D9BFQ28550966-8654E11C-B199-4E2F-94CE-F394F67DAC9FQ35537249-C9F6FA6C-D505-4F8D-918D-65F0E4CEAEFDQ35689553-3F740F83-EA9B-4730-9217-AA3598B2AB1BQ35715098-83BA8C3E-FF0D-4EE9-B425-EA5283D64CBFQ36436616-B6A1CCDE-246A-4856-9BAD-BEA55E9E7EE3Q38222647-48454891-C0CC-45DF-9D05-13BDA0EF56C4Q38672535-F157C863-26D5-4C6A-B607-2B59F00AA0B3Q38783934-427558F0-5514-4189-8BEE-127634806DFBQ39021656-A7F92291-C68F-491A-89CA-00F556376033Q42935757-E3896568-D408-4E1E-AB66-3D76BD0F3A63Q43530589-E6E6E074-05C8-4343-9912-25FA47AA77EBQ43588566-5A639878-7305-4E6D-A9DC-4AD848D9F928Q43969793-BAE81A0E-66AD-48A0-B805-D0D0B89831D5Q45082517-2BD6E4C3-46D9-4793-B3F8-F960630B7ED9Q45167957-57AFC2AA-EF98-451F-9243-9C8C4C899018Q45779270-6F1948BD-7DAD-444C-B0CC-EF383F6EC0E6Q46005917-7095F4E1-91B0-4862-9B66-946ECDD108F0Q46148290-ADC374B1-78F6-44ED-A026-7BACFB19D41FQ46221261-0C47B9EA-DEAF-47E6-932E-2D97D8489220Q46287790-8A2F061B-D0FC-46EE-B97D-2C551A271743Q46320464-E2BB8514-31CC-439A-A079-2316E8B7C04AQ46342337-16C16DBE-4C66-4ADC-92C9-6C13AD39B49AQ46490530-69A1DD51-C909-4AFA-963B-E66817714D61Q46499279-F508E045-2481-4953-9781-265D3F539F65Q46503501-20A9200D-09DB-435A-829B-9071664F663DQ46586485-BBECF34D-5521-406C-8651-2D80371C35E8Q46825105-30972031-C7D3-4456-B3D5-2ED70B8EA166Q46979277-1CFBD1E4-0929-45ED-9903-34394E69AE10Q46987591-D1DD8A26-98FE-4044-AC76-D36E2B333A1AQ46987949-96534318-F231-489A-963A-24280D81E5A4Q47200422-1B8600BB-876B-4C69-A74E-F233F5B64C65Q47802398-DC367E7A-1DA4-463D-ADA9-3659F019D70EQ47837178-817D52F7-C33C-4FB6-80CD-26B258EDE8EFQ48053144-EA36818E-0221-43FB-8420-AC1C448E4CADQ48093181-E73C8E84-F5FE-49BB-9864-152BCA573F09Q48130128-BE214A90-3AE2-49F8-AD65-4404A12198BEQ48168147-FE7D214D-B2A3-4FA4-AFF5-0309091784CCQ48216061-953C5070-B8AC-420F-A6D9-1A7F98C1E97BQ48268823-249720A2-1FDA-4B67-9E91-C80C50EDD15B
P50
description
Australian polymer chemist
@en
química australiana
@ast
química australiana
@ca
scheikundige uit Australië
@nl
كيميائية أسترالية
@ar
name
Michelle Coote
@ast
Michelle Coote
@ca
Michelle Coote
@de
Michelle Coote
@en
Michelle Coote
@es
Michelle Coote
@fr
Michelle Coote
@ga
Michelle Coote
@it
Michelle Coote
@nl
Michelle Coote
@sl
type
label
Michelle Coote
@ast
Michelle Coote
@ca
Michelle Coote
@de
Michelle Coote
@en
Michelle Coote
@es
Michelle Coote
@fr
Michelle Coote
@ga
Michelle Coote
@it
Michelle Coote
@nl
Michelle Coote
@sl
prefLabel
Michelle Coote
@ast
Michelle Coote
@ca
Michelle Coote
@de
Michelle Coote
@en
Michelle Coote
@es
Michelle Coote
@fr
Michelle Coote
@ga
Michelle Coote
@it
Michelle Coote
@nl
Michelle Coote
@sl
P166
P1053
B-2267-2010
P106
P1412
P166
P21
P27
P31
P3829
P496
0000-0003-0828-7053
P569
2000-01-01T00:00:00Z