about
Excited state dynamics of a PtII diimine complex bearing a naphthalene-diimide electron acceptor.Dinitrogen release from arylpentazole: a picosecond time-resolved infrared, spectroelectrochemical, and DFT computational study.From intercalation to groove binding: switching the DNA-binding mode of isostructural transition-metal complexes.Electron transfer dynamics and excited state branching in a charge-transfer platinum(II) donor-bridge-acceptor assembly.Toward control of electron transfer in donor-acceptor molecules by bond-specific infrared excitation.On the mechanism of vibrational control of light-induced charge transfer in donor-bridge-acceptor assemblies.Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis.Structure of the complex of [Ru(tpm)(dppz)py](2+) with a B-DNA oligonucleotide - a single-substituent binding switch for a metallo-intercalator.A ratiometric sensor for DNA based on a dual emission Ru(dppz) light-switch complex.Dinuclear osmium(II) probes for high-resolution visualisation of cellular DNA structure using electron microscopy.A re-investigation of [Fe(L-cysteinate)2(CO)2]2-: an example of non-heme CO coordination of possible relevance to CO binding to ion channel receptors.[Mn(CO)4{S2CNMe(CH2CO2H)}], a new water-soluble CO-releasing molecule.Highly enantioselective metallation-substitution alpha to a chiral nitrileA characterization of the Raman modes in a J-aggregate-forming dye: a comparison between theory and experiment.Structure and ultrafast dynamics of the charge-transfer excited state and redox activity of the ground state of mono- and binuclear platinum(II) diimine catecholate and bis-catecholate complexes: a transient absorption, TRIR, DFT, and electrochemicaDiastereoselective cycloadditions and transformations of N-alkyl and N-aryl maleimides with chiral 9-anthrylethanol derivatives.Photophysical properties and singlet oxygen production by ruthenium(II) complexes of benzo[i]dipyrido[3,2-a:2',3'-c]phenazine: spectroscopic and TD-DFT study.A copper(I)-arene complex with an unsupported η6 interaction.Identification of the reactive cis,mer isomer of [Ir(CO)2I3Me]-: relation to the mechanism of iridium-catalyzed methanol carbonylation.Ionisation of the zinc--iodine bond of alkylzinc iodides in dimethylformamide from theory and experiment.Manganese Tricarbonyl Complexes with Asymmetric 2-Iminopyridine Ligands: Toward Decoupling Steric and Electronic Factors in Electrocatalytic CO2 Reduction.(13)C or Not (13)C: Selective Synthesis of Asymmetric Carbon-13-Labeled Platinum(II) cis-Acetylides.Collision-induced conformational changes in glycine.Reactivity of Ir(III) carbonyl complexes with water: alternative by-product formation pathways in catalytic methanol carbonylation.Shape-, size-, and functional group-selective binding of small organic guests in a paramagnetic coordination cage.Directing the path of light-induced electron transfer at a molecular fork using vibrational excitation.Hydrogen Tunneling above Room Temperature Evidenced by Infrared Ion Spectroscopy.Ergothioneine and related histidine derivatives in the gas phase: tautomer structures determined by IRMPD spectroscopy and theory.Studies on the stereochemical assignment of 3-acylidene 2-oxindoles.Synthesis, characterization, and DNA binding properties of ruthenium(II) complexes containing the redox active ligand benzo[i]dipyrido[3,2-a:2',3'-c]phenazine-11,16-quinone.Homoleptic low-valent polyazides of group 14 elements.State-to-state reaction probabilities for the H+O2(v,j)-->O+OH(v',j') reaction on three potential energy surfaces.A Self-Assembled Metallomacrocycle Singlet Oxygen Sensitizer for Photodynamic Therapy.Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.Turning intercalators into groove binders: synthesis, photophysics and DNA binding properties of tetracationic mononuclear ruthenium(ii)-based chromophore–quencher complexesGas-phase complexes of Ni 2+ and Ca 2+ with deprotonated histidylhistidine (HisHis): A model case for polyhistidyl-metal binding motifsChemInform Abstract: A Strategy Toward the Biomimetic Synthesis of (.+-.)-Morusalbanol A Pentamethyl EtherA Strategy toward the Biomimetic Synthesis of (±)-Morusalbanol A Pentamethyl EtherMechanistic insight into proton-coupled mixed valencyStructural, spectroscopic and theoretical studies of a diruthenium(II,II) tetraformamidinate that reversibly binds dioxygen
P50
Q33378330-08323513-D13E-47CC-A55E-64694B50E5F2Q35041723-5604AAA5-08CE-4AE4-ABD2-143115D5997EQ35134070-73E6E189-9EF4-4C8C-92B2-9C1B60CA9BA2Q35383609-A5E09B3B-BD73-4463-9CAD-BE7DCEA8C9CAQ35530599-897F2031-2ACD-47E6-811B-A6E615540F7BQ35751382-5EA623FB-7FD6-424A-960E-F2A0884BDD6EQ37676294-250E92E2-39E7-45EC-B689-82357C35F380Q38346920-2C8722CF-D2ED-47E3-8550-99111148B661Q38826924-199838BC-E743-463B-9FFC-8C1379B2BF10Q38958811-491D9DED-5A62-40F7-AFAC-46819E19C2A1Q39506360-E6F69AF6-15C0-41FE-84E8-BCD30613470CQ39576090-EE3AC800-93B2-4D8B-B61C-BDB779463967Q42219394-BBE7F045-58B8-4FDE-82C9-4C3252995EF3Q42859225-FFEDB347-A18F-474D-87A3-A1B8529289E8Q42875503-B82CD207-DEE7-4914-9705-6F9B851E6E6AQ42926297-7E69A212-D1C5-4FD8-934F-45359292291AQ43269217-40D4302C-4DA6-481A-AF23-650751488F0BQ46020056-DD7178D6-B8B8-4A0B-ADA2-AA57F9E807D7Q46211115-941DB14A-23CB-4728-9ED4-6A7A8ADC8F3BQ46367451-D1D31A5A-7BEA-4640-81AE-3F18A4F3246CQ46443871-7F8BA311-945C-48C2-8304-3B0CFA79724BQ46504403-DA63FB62-EC2F-4B0A-B496-0D33256632BFQ46612062-DEA1F65F-1600-45BB-86BD-F8D3F68F2797Q46989809-5885E077-2FE5-45E2-84CC-BC6B1AA61E89Q47261653-E84E2747-CB57-48E3-9E24-C1AF3940782FQ48050876-A543B340-781C-4648-9ECB-47DB862B6E78Q48138710-924B0AE8-6673-4E5E-9F26-B0CD8F230B1FQ48210450-0D01DEBC-63BE-409E-84BC-CDD430C7C05AQ50223706-5628570F-3027-4CDE-8CDF-9DEEEA3EB187Q50506529-29D22F88-55EA-4C10-8A1E-4AAFDE7D7007Q50998867-737AC4B5-6307-4058-9EEA-176B29FE3A5BQ51907686-AD67D3A9-743C-49D4-935D-0E99085150F7Q54136394-44D3220D-A7DA-4FFC-BC28-8B53543D8318Q55081751-0B4E66C0-84D3-4DE5-9A6A-885AF9D78D92Q56880779-36FE335E-E955-4A75-808E-78D8014A94B2Q56880780-DAC41E0E-97C2-4663-9D27-8D565C4FB5A4Q56880783-9B7FD696-0268-447E-96D9-02338EF93CD1Q56880785-0E53B8A9-AB61-4EC9-8E43-3CB65F62D07BQ56880787-605DC90E-6DBF-4B81-8F20-156573AF71E0Q56880788-166ADECE-2D67-49D3-98C7-B671E8ACB637
P50
description
researcher from The Netherlands
@en
wetenschapper
@nl
name
Anthony J. H. M. Meijer
@ast
Anthony J. H. M. Meijer
@en
Anthony J. H. M. Meijer
@es
Anthony J. H. M. Meijer
@nl
type
label
Anthony J. H. M. Meijer
@ast
Anthony J. H. M. Meijer
@en
Anthony J. H. M. Meijer
@es
Anthony J. H. M. Meijer
@nl
prefLabel
Anthony J. H. M. Meijer
@ast
Anthony J. H. M. Meijer
@en
Anthony J. H. M. Meijer
@es
Anthony J. H. M. Meijer
@nl
P1053
I-9513-2012
P106
P1153
7102504724
P2002
DrAnthonyMeijer
P21
P31
P3829
P496
0000-0003-4803-3488