DNA interactions and photocatalytic strand cleavage by artificial nucleases based on water-soluble gold(III) porphyrins.Artificial enzyme catalysis controlled and driven by light.Functionalized derivatives of 1,4-dimethylnaphthalene as precursors for biomedical applications: synthesis, structures, spectroscopy and photochemical activation in the presence of dioxygen.A water soluble tri-cationic porphyrin-EDTA conjugate induces apoptosis in human neuroendocrine tumor cell lines.Design, synthesis and characterization of a modular bridging ligand platform for bio-inspired hydrogen production.Origin of proton affinity to membrane/water interfacesTwo-electron carbon dioxide reduction catalyzed by rhenium(I) bis(imino)acenaphthene carbonyl complexes.Rhodium-coordinated poly(arylene-ethynylene)-alt-poly(arylene-vinylene) copolymer acting as photocatalyst for visible-light-powered NAD⁺/NADH reduction.Suzuki-Miyaura cross-coupling reaction on copper-trans-A(2)B corroles with excellent functional group tolerance.Synthesis and characterization of redox-active charge-transfer complexes with 2,3,5,6-tetracyanopyridine (TCNPy) for the photogeneration of pyridinium radicals.Electrocatalytic Reduction of Carbon Dioxide to Carbon Monoxide by a Polymerized Film of an Alkynyl-Substituted Rhenium(I) Complex.Tetra-kis(triphenyl-arsine)copper(I) hexa-fluoridophosphate.Photocatalytic reduction of artificial and natural nucleotide co-factors with a chlorophyll-like tin-dihydroporphyrin sensitizer.Synthesis and characterisation of cobalt, nickel and copper complexes with tripodal 4N ligands as novel catalysts for the homogeneous partial oxidation of alkanes.Spontaneous nucleophilic addition of hydroxide ions to the meso-position of high-valent antimony-oxo porphyrin complexes.Bionic catalyst design: a photochemical approach to artificial enzyme function.The Tetracyanopyridinide Dimer Dianion, σ-[TCNPy]2 (2.).Stable Europium(III) Complexes with Short Linkers for Site-Specific Labeling of Biomolecules.Characterization of Tetracyanopyridine (TCNPy)-Based Magnets: V[TCNPy]2 ⋅z (CH2 Cl2 ) (Tc =111 K) and V[TCNPy]3 ⋅z (CH2 Cl2 ) (Tc =90 K).Evidence for photosensitised hydrogen production from water in the absence of precious metals, redox-mediators and co-catalysts.Syntheses, emission properties and intramolecular ligand exchange of zinc complexes with ligands belonging to the tmpa family.Characterization of a non-aggregating silicon(IV) phthalocyanine in aqueous solution: toward red-light-driven photocatalysis based on earth-abundant materials.Determination of 3J(1H3′31P) couplings in a DNA oligomer with enhanced sensitivity employing a constant-time TOCSY difference experimentElectrocatalytic and photocatalytic reduction of carbon dioxide to carbon monoxide using the alkynyl-substituted rhenium(I) complex (5,5′-bisphenylethynyl-2,2′-bipyridyl)Re(CO)3ClLuminescence and spectroscopic studies of organometallic rhodium and rhenium multichromophore systems carrying polypyridyl acceptor sites and phenylethynyl antenna subunitsAnthracene Based Conjugated Polymers: Correlation between π−π-Stacking Ability, Photophysical Properties, Charge Carrier Mobility, and Photovoltaic PerformanceRecent progress in homogeneous multielectron transfer photocatalysis and artificial photosynthetic solar energy conversionSynthesis and Characterization of Novel Re(BIAN)(CO)3Cl Derivatives Including the First Example of a Water-soluble Tricarbonyl Rhenium(I) Complex with Bis(imino)acenaphthene LigandsSynthesis and Characterization of a Stable Bismuth(III) A3–CorrolePhotocatalytic reactions of porphyrin-based multielectron transfer sensitizersSuppressing Effect of 2-Nitrobenzaldehyde on Singlet Oxygen Generation, Fatty Acid Photooxidation, and Dye-Sensitizer DegradationSpin-Forbidden Excitation: A New Approach for Triggering Photopharmacological Processes with Low-Intensity NIR LightHow [FeFe]-Hydrogenase Facilitates Bidirectional Proton Transfer
P50
Q33453524-03EFC6DB-854E-4750-AB25-7910BE6F791CQ37299497-DD495793-15C1-4411-AE81-70BFF57ABA0BQ39305359-0DF972A0-1AC0-43AC-A186-F83722BC983AQ39453532-51168FB3-E5FF-4C40-9E38-1D3D1E856571Q39643942-3BE2815B-BEB1-4311-9E9A-763CF2112F37Q40971915-9BEE4741-3B5F-4B85-AA1E-5F93E5D3F1B5Q41144455-12142A42-D6A4-4995-929F-A98EE340868BQ41841286-CD9CD871-F0C2-4083-A54F-0062FDAA4257Q41893179-6101221F-718A-4A8F-9B17-5C82D0C6BC1BQ41959543-0FD9857B-0B95-4DB3-B400-2FE24F38F16EQ42220896-930A1DFE-09E8-4EA4-861B-02C7C927A850Q42588600-827615D3-8235-4515-95FE-3630FF499697Q42938432-36269744-C64D-4108-9E0F-D359DD23E1AEQ43120041-CBF15840-D4A3-4D67-A386-8873A581252AQ43618323-3BABE302-47D9-4297-A6AD-D6E42A624783Q43877264-6093FB01-9329-4562-B423-AE02F067AB83Q45937741-275040E0-7F21-4900-93FC-EFCCB449239FQ47140402-EC1ECB17-3DD2-4961-8B07-A846F7D67050Q48109706-0817A131-DABC-409D-832D-CE7AA12C96B2Q48263500-76F05653-BBC3-48DE-A10C-2EC21F229E6DQ50279353-19200123-E4BB-425E-B8AD-D4A60C3CFD67Q50487572-231689EB-7787-488A-878F-1CE4B81DF85CQ57652248-2B7AD478-F23B-4900-9E91-20AB2FDE0E5CQ58911620-FB7DF31B-FB3A-454F-9FCD-BA1C332C3AD6Q58911695-B2C7E18C-60DF-4EEF-BA29-8804142C6BCBQ58911733-858FD19D-D98B-4A0F-ABF1-F0EDCD22AFCCQ59256073-DE6F6D9A-5400-4A1D-99C3-6BC2205A30F9Q59256083-DBD2F1C6-178D-49C5-ACB3-6B2342501925Q59256100-A5C9A803-3AC4-4E9D-9C84-D6DA4639AE43Q59256121-DDD7E3FF-BB9C-49AE-B891-CCFF5713E8FDQ60949345-6FD11338-DA51-4A78-AD1D-748726FC9177Q89833595-D3CED56E-A11B-41A3-BD02-16919E4221FDQ90455254-9B3C3A4E-7C61-42E1-9601-B118ACC5703F
P50
description
Duits scheikundige
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German chemist
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German chemist
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German chemist
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Saksamaa keemik
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ceimiceoir Gearmánach
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chimist german
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chimiste allemand
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deutscher Chemiker, Leiter des Instituts für Anorganische Chemie
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kimist gjerman
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Günther Knör
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Guenther Knoer
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Guenther Knor
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Gunther Knoer
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Gunther Knor
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Gunther Knor
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Günther Knör
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Günther Knör
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Günther Knör
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Günther Knör
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P1053
A-9802-2011
P1153
6701315647
P1412
P1559
Günther Knör
@de
P19
P21
P2381
P31
P373
Günther Knör
P3829
P496
0000-0002-2259-6496
P569
1965-01-01T00:00:00Z