What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Chemical reaction
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.
His most cited work include:
- How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution (949 citations)
- Flavonoids as Antioxidants (907 citations)
- Reaction pathways and mechanisms of photodegradation of pesticides. (432 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Photochemistry (65.44%)
- Radical (35.48%)
- Aqueous solution (28.57%)
What were the highlights of his more recent work (between 2000-2010)?
- Photochemistry (65.44%)
- Radical (35.48%)
- Radical ion (16.13%)
In recent papers he was focusing on the following fields of study:
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.
Between 2000 and 2010, his most popular works were:
- Reaction pathways and mechanisms of photodegradation of pesticides. (432 citations)
- How curcumin works preferentially with water soluble antioxidants. (213 citations)
- Ferrocenyl‐Functionalised Terpyridines and Their Transition‐Metal Complexes: Syntheses, Structures and Spectroscopic and Electrochemical Properties (63 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Chemical reaction
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.
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