Steen Steenken mainly investigates Photochemistry, Radical, Radiolysis, Aqueous solution and Medicinal chemistry. His study in the field of Electron transfer also crosses realms of Flash photolysis. His Radical research integrates issues from Inorganic chemistry, Redox, Ring, Adduct and Oxidizing agent.
His study in Radiolysis is interdisciplinary in nature, drawing from both Photodissociation, Radiation chemistry, Heterolysis and Pyrimidine. He has included themes like Yield, Guanosine and DNA in his Aqueous solution study. His biological study spans a wide range of topics, including Radical ion, Electrophile and Nucleophile.
Steen Steenken spends much of his time researching Photochemistry, Radical, Aqueous solution, Radiolysis and Flash photolysis. He interconnects Radical ion and Protonation in the investigation of issues within Photochemistry. His Radical research is multidisciplinary, incorporating perspectives in Yield, Medicinal chemistry, Inorganic chemistry, Redox and Adduct.
His research in Medicinal chemistry focuses on subjects like Stereochemistry, which are connected to Cytosine. The various areas that Steen Steenken examines in his Aqueous solution study include Oxidizing agent, Electron paramagnetic resonance and Decarboxylation. His work on Solvated electron as part of general Radiolysis research is frequently linked to Pulse and One-electron reduction, bridging the gap between disciplines.
His scientific interests lie mostly in Photochemistry, Radical, Radical ion, Aqueous solution and Deprotonation. In the field of Photochemistry, his study on Electron transfer overlaps with subjects such as Flash photolysis. His work is dedicated to discovering how Radical, Redox are connected with Active site, Imidazole, Vitamin C and Curcumin and other disciplines.
His research investigates the link between Radical ion and topics such as Stereochemistry that cross with problems in Thymine, Computational chemistry, Guanosine, DNA Strand Break and Deoxyribose. His work deals with themes such as Electrophile and Reactivity, which intersect with Aqueous solution. The concepts of his Radiolysis study are interwoven with issues in Photodissociation and Antioxidant.
His primary scientific interests are in Photochemistry, Heterolysis, Radiolysis, Radical and Cytosine. His Photochemistry research includes themes of Intramolecular force, Terpyridine and Transition metal. His Heterolysis study combines topics from a wide range of disciplines, such as Homolysis and Bond cleavage.
His studies in Radiolysis integrate themes in fields like Photocatalysis, Photodegradation, Photodissociation, Curcumin and Vitamin C. In his work, he performs multidisciplinary research in Radical and Flash photolysis. His Cytosine study incorporates themes from Radical ion, Protonation, Base pair, Hydrogen bond and Deprotonation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution
Steen Steenken;Slobodan V. Jovanovic.
Journal of the American Chemical Society (1997)
Flavonoids as Antioxidants
Slobodan V. Jovanovic;Steen Steenken;Mihajlo Tosic;Budimir Marjanovic.
Journal of the American Chemical Society (1994)
Reaction pathways and mechanisms of photodegradation of pesticides.
H.D. Burrows;J.A. Santaballa;S. Steenken.
Journal of Photochemistry and Photobiology B-biology (2002)
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.
Journal of The Chemical Society-perkin Transactions 1 (1996)
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.
H-Atom Transfer Is A Preferred Antioxidant Mechanism of Curcumin
Slobodan V. Jovanovic;Steen Steenken;and Charles W. Boone;Michael G. Simic.
Journal of the American Chemical Society (1999)
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.
Journal of the American Chemical Society (1992)
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.
Journal of the American Chemical Society (2000)
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 Journal of Physical Chemistry (1975)
Antioxidant potential of gallocatechins. A pulse radiolysis and laser photolysis study
Slobodan V. Jovanovic;Yukihiko Hara;Steen Steenken;Michael G. Simic.
Journal of the American Chemical Society (1995)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: