about
Spectroscopic study of jet-cooled deuterated porphycenes: unusual isotopic effects on proton tunneling.Surface-enhanced Raman spectroscopy introduced into the International Standard Organization (ISO) regulations as an alternative method for detection and identification of pathogens in the food industry.Spectroscopy and Tautomerization Studies of Porphycenes.Solvent-Induced Changes in Photophysics and Photostability of Indole-Naphthyridines.Near-Field Enhanced Photochemistry of Single Molecules in a Scanning Tunneling Microscope Junction.Improved Method of Fluorescence Quantum Yield Determination.Spectroscopic and microscopic investigations of tautomerization in porphycenes: condensed phases, supersonic jets, and single molecule studies.Parent, Unsubstituted Hemiporphycene: Synthesis and Properties.Near Infrared Phosphorescent, Non-oxidizable Palladium and Platinum Perfluoro-phthalocyanines.Detection of a weak ring current in a nonaromatic porphyrin nanoring using magnetic circular dichroism.Enhancing fluorescence by using pluronic block copolymers as carriers of monomeric porphycenes.Evidence for Dominant Role of Tunneling in Condensed Phases and at High Temperatures: Double Hydrogen Transfer in Porphycenes.In Search for the Best Environment for Single Molecule Studies: Photostability of Single Terrylenediimide Molecules in Various Polymer Matrices.Anharmonicity in a double hydrogen transfer reaction studied in a single porphycene molecule on a Cu(110) surface.Two macrocycles in one shot: Synthesis, spectroscopy, photophysics, and tautomerism of 23-oxahemiporphycene and 5 carbaldehyde-21-oxacorrole.Hot Carrier-Induced Tautomerization within a Single Porphycene Molecule on Cu(111).Tailored gold nanostructure arrays as catalysts for oxygen reduction in alkaline media and a single molecule SERS platform.Non-typical fluorescence studies of excited and ground state proton and hydrogen transfer.Unusual effects in single molecule tautomerization: hemiporphyceneNature of Large Temporal Fluctuations of Hydrogen Transfer Rates in Single MoleculesCombined effect of hydrogen bonding interactions and freezing of rotameric equilibrium on the enhancement of photostabilityTriarylisocyanurate-Based Fluorescent Two-Photon AbsorbersVersatile Approach for Reliable Determination of Both High and Low Values of Luminescence Quantum YieldsAntiaromatic or Nonaromatic? 21 H,61 H-2,6(2,5)-Dipyrrola-1,5(2,6)-dipyridinacyclooctaphane-3,7-diene: a Porphycene Derivative with 4 N π ElectronsPhotoinduced oxidation of an indole derivative: 2-(1'H-indol-2'-yl)-[1,5]naphthyridineGoodbye to Quinine in Sulfuric Acid Solutions as a Fluorescence Quantum Yield StandardNear-Field Spectral Response of Optically Excited Scanning Tunneling Microscope Junctions Probed by Single-Molecule Action Spectroscopy
P50
Q35227997-E4ECFB94-789F-48E7-82CD-32B7FDAC974EQ37639728-2429B692-FF4E-49C3-8ECB-9A4856ACBD0BQ38911244-7F5D23EC-1120-47AF-B524-E83748D6E65BQ46788714-62BEDF76-913E-4248-A5CE-9CE32DA591F6Q47572817-EF3CC91E-6991-4D82-977A-8206794CEB13Q47745835-210AA095-19B0-4230-94F3-ED3EE8F7B86EQ47982008-80176794-18E0-40AB-AF81-85B367F60E99Q48053620-E4FF324F-EA0A-4F9D-ACFC-0FF5262A5514Q48252902-304C1F7B-E667-435E-98EB-C974686129BAQ49498959-22DFECF1-4C79-4BA6-91D5-488953C19C3CQ49926874-0485BDF3-562A-436E-86AF-709A6979A92CQ50744157-A352E8FB-B6C0-4E25-B86D-D90B7F4459A6Q50868280-B31C75E6-70FD-4AF4-A725-4778FD7D514EQ52314477-68D6DBF3-B7DB-4F4E-9C94-D2B0F07452D2Q52577674-24B7B1CF-4E01-4EAC-B85B-F11E445ACB8AQ53174505-29A9A78F-CEB6-455A-B7BB-A0C40A3CBF57Q53481353-84B6CB33-2F20-41AC-95FF-677D6AF91740Q53792091-A308E2C4-73D1-4FEE-B191-1DD13B9B5D35Q57472206-4A5E9B3C-B67B-4EE6-9A2B-75CFACEB3DE0Q87848599-51D05D1A-FB21-441F-AB11-AA7688600A5AQ88538431-86DCE8E9-D67E-47F0-A226-08785CF532C1Q89971370-762FA843-E6BE-4129-B2DB-411454C1F499Q90772101-DCF0CD41-97A8-494D-B645-03497930E35AQ92034092-2E979C45-14BC-4C07-8660-EA38711FF770Q92524565-D0402996-794C-478F-86A2-517DC35AF58FQ92592509-8BAA31F9-883D-4C5B-A0AF-78BD017A8D4CQ92966141-A838F5E5-AA39-468F-90F4-86604B88B79E
P50
description
researcher ORCID ID = 0000-0001-5745-583X
@en
wetenschapper
@nl
name
Jacek Waluk
@ast
Jacek Waluk
@en
Jacek Waluk
@es
Jacek Waluk
@nl
type
label
Jacek Waluk
@ast
Jacek Waluk
@en
Jacek Waluk
@es
Jacek Waluk
@nl
prefLabel
Jacek Waluk
@ast
Jacek Waluk
@en
Jacek Waluk
@es
Jacek Waluk
@nl
P106
P21
P31
P496
0000-0001-5745-583X