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Steen Steenken

Steen Steenken

D-Index & Metrics

Chemistry

D-Index
70
Citations
20502
World Ranking
5779
National Ranking
425

Overview

Steen Steenken is affiliated with the Max Planck Society in Germany. Their work is situated within a leading research organization known for its contributions to scientific advancement across various disciplines.

There are no records of recent papers, frequent co-authors, or frequent publication venues associated with Steen Steenken, which suggests limited publicly available information on recent scientific outputs or collaboration networks. Similarly, no data is available concerning book publications or specific fields, subfields, or topics of research indicated in connection with their work.

Steenken's profile does not list any awards or honors, and there is no information about deceased status, indicating an active professional status without recorded accolades or distinctions in the provided dataset.

Given the affiliation with the Max Planck Society, it can be inferred that Steenken is engaged in research activities in a robust scientific environment. However, detailed specifics regarding their academic focus, research topics, and publication history are not publicly documented here.

Best Publications

  • How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution

    Steen Steenken;Slobodan V. Jovanovic

  • Flavonoids as Antioxidants

    Slobodan V. Jovanovic;Steen Steenken;Mihajlo Tosic;Budimir Marjanovic

  • Reaction pathways and mechanisms of photodegradation of pesticides.

    H.D. Burrows;J.A. Santaballa;S. Steenken

  • Standard electrode potentials involving radicals in aqueous solution: Inorganic radicals

    David A. Armstrong;Robert E. Huie;Willem H. Koppenol;Sergei V. Lymar

  • One-electron redox potentials of phenols. Hydroxy- and aminophenols and related compounds of biological interest

    S. Steenken;P. Neta

  • H-Atom Transfer Is A Preferred Antioxidant Mechanism of Curcumin

    Slobodan V. Jovanovic;Steen Steenken;and Charles W. Boone;Michael G. Simic

  • Reduction potentials of flavonoid and model phenoxyl radicals. Which ring in flavonoids is responsible for antioxidant activity

    Slobodan V. Jovanovic;Steen Steenken;Yukihiko Hara;Michael G. Simic

  • Formation of 8-hydroxy(deoxy)guanosine and generation of strand breaks at guanine residues in DNA by singlet oxygen

    Thomas P. A. Devasagayam;Steen Steenken;Maik S. W. Obendorf;Wolfgang A. Schulz

  • Structure and acid-base properties of one-electron-oxidized deoxyguanosine, guanosine, and 1-methylguanosine

    Unknown

  • Formation of radical cations of methoxylated benzenes by reaction with hydroxyl radicals, thallium(2+), silver(2+), and peroxysulfate (SO4.-) in aqueous solution. Optical and conductometric pulse radiolysis and in situ radiolysis electron spin resonance study

    P. O'Neill;S. Steenken;D. Schulte-Frohlinde

  • The trap depth (in DNA) of 8-oxo-7,8-dihydro-2'deoxyguanosine as derived from electron-transfer equilibria in aqueous solution

    Steen Steenken;Slobodan V. Jovanovic;Massimo Bietti;Klaus Bernhard

  • One-electron-reduction potentials of pyrimidine bases, nucleosides, and nucleotides in aqueous solution. Consequences for DNA redox chemistry

    S. Steenken;J. P. Telo;H. M. Novais;L. P. Candeias

  • Reaction of HO* with guanine derivatives in aqueous solution: formation of two different redox-active OH-adduct radicals and their unimolecular transformation reactions. Properties of G(-H)*.

    Luis P. Candeias;Steen Steenken

  • Antioxidant potential of gallocatechins. A pulse radiolysis and laser photolysis study

    Slobodan V. Jovanovic;Yukihiko Hara;Steen Steenken;Michael G. Simic

  • How curcumin works preferentially with water soluble antioxidants.

    Slobodan V. Jovanovic;Charles W. Boone;Steen Steenken;Manuela Trinoga

  • Pattern of hydroxyl radical addition to uracil and methyl- and carboxyl-substituted uracils. Electron transfer of hydroxyl adducts with N,N,N',N'-tetramethyl-p-phenylenediamine and tetranitromethane

    Unknown

  • Reaction of tert-butoxy radicals with phenols. Comparison with the reactions of carbonyl triplets

    P. K. Das;M. V. Encinas;S. Steenken;J. C. Scaiano

  • Electron-Transfer-Induced Acidity/Basicity and Reactivity Changes of Purine and Pyrimidine Bases. Consequences of Redox Processes for Dna Base Pairs

    Steen Steenken

  • Antioxidant properties of flavonoids: reduction potentials and electron transfer reactions of flavonoid radicals

    S.V. Jovanovic;S. Steenken;M.G. Simic;Y. Hara

  • Ionization of purine nucleosides and nucleotides and their components by 193-nm laser photolysis in aqueous solution: model studies for oxidative damage of DNA

    Unknown

  • Electron transfer in di(deoxy)nucleoside phosphates in aqueous solution: rapid migration of oxidative damage (via adenine) to guanine

    Luis Pedro Candeias;Steen Steenken

  • Photo-heterolysis and -homolysis of substituted diphenylmethyl halides, acetates, and phenyl ethers in acetonitrile : characterization of diphenylmethyl cations and radicals generated by 248-nm laser flash photolysis

    Joerg Bartl;S. Steenken;Herbert Mayr;R. A. McClelland

  • Pattern of OH radical reaction with adenine and its nucleosides and nucleotides. Characterization of two types of isomeric OH adduct and their unimolecular transformation reactions

    A.J.S.C. Vieira;S. Steenken

Frequent Co-Authors

Dietrich Schulte-Frohlinde
Dietrich Schulte-Frohlinde Max Planck Society
Jochen Mattay
Jochen Mattay Bielefeld University
Joaquim L. Faria
Joaquim L. Faria University of Porto
Karl Wieghardt
Karl Wieghardt Max Planck Society
Herbert Mayr
Herbert Mayr Ludwig-Maximilians-Universität München
Waldemar Adam
Waldemar Adam University of Würzburg
Helmut Sies
Helmut Sies Heinrich Heine University Düsseldorf
Clemens von Sonntag
Clemens von Sonntag Max Planck Society
Eberhard Bothe
Eberhard Bothe Max Planck Society
Wolfgang A. Schulz
Wolfgang A. Schulz Heinrich Heine University Düsseldorf

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