What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Molecule
Atsuhiro Osuka spends much of his time researching Porphyrin, Photochemistry, Crystallography, Stereochemistry and Aromaticity.
His work carried out in the field of Porphyrin brings together such families of science as Zinc, Ultrafast laser spectroscopy, Dimer, Molecule and Intramolecular force.
His Photochemistry research is multidisciplinary, incorporating perspectives in Fluorescence spectroscopy, Two-photon absorption, Excited state, Singlet state and Absorption spectroscopy.
His Crystallography research integrates issues from Dihedral angle, Proton NMR, Pentamer and Trimer.
His Stereochemistry study deals with Aryl intersecting with Medicinal chemistry.
His research integrates issues of Absorption and Pyrrole in his study of Aromaticity.
His most cited work include:
- Fully conjugated porphyrin tapes with electronic absorption bands that reach into infrared. (639 citations)
- Discrete cyclic porphyrin arrays as artificial light-harvesting antenna. (390 citations)
- Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities (385 citations)
What are the main themes of his work throughout his whole career to date?
Photochemistry, Porphyrin, Crystallography, Organic chemistry and Stereochemistry are his primary areas of study.
His Photochemistry study combines topics in areas such as Excited state, Intramolecular force, Fluorescence and Aromaticity.
The Aromaticity study combines topics in areas such as Metalation and Computational chemistry.
His research in Porphyrin intersects with topics in Zinc, Polymer chemistry, Dimer, Molecule and Absorption spectroscopy.
His Crystallography study frequently draws connections to adjacent fields such as Absorption.
His Aryl research includes elements of Medicinal chemistry and Palladium.
He most often published in these fields:
- Photochemistry (41.46%)
- Porphyrin (40.60%)
- Crystallography (18.62%)
What were the highlights of his more recent work (between 2015-2021)?
- Crystallography (18.62%)
- Photochemistry (41.46%)
- Porphyrin (40.60%)
In recent papers he was focusing on the following fields of study:
His main research concerns Crystallography, Photochemistry, Porphyrin, Dimer and Aromaticity.
The concepts of his Crystallography study are interwoven with issues in Absorption, Molecule, Corrole and Stereochemistry.
His studies deal with areas such as Delocalized electron, Ultrafast laser spectroscopy, Fluorescence, Excited state and Intramolecular force as well as Photochemistry.
Atsuhiro Osuka usually deals with Porphyrin and limits it to topics linked to Radical and Monomer.
His Dimer course of study focuses on Polymer chemistry and Boron, Palladium, Catalysis, Borylation and Metal.
His Aromaticity research includes themes of Computational chemistry and Triplet state.
Between 2015 and 2021, his most popular works were:
- Chemistry of meso-Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist. (146 citations)
- Metal-Free Approach to Biaryls from Phenols and Aryl Sulfoxides by Temporarily Sulfur-Tethered Regioselective C–H/C–H Coupling (81 citations)
- Fully Fused Quinoidal/Aromatic Carbazole Macrocycles with Poly-radical Characters. (41 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Molecule
His primary areas of study are Photochemistry, Porphyrin, Crystallography, Aromaticity and Antiaromaticity.
He combines subjects such as Excited state, Dimer, Delocalized electron and Radical with his study of Photochemistry.
The Porphyrin study combines topics in areas such as Conjugated system, Ring, Ground state, Absorption and Absorption spectroscopy.
His Crystallography research integrates issues from Thiophene, Phenylene, Thiophenol and Walden inversion.
His work carried out in the field of Aromaticity brings together such families of science as Excited singlet, Reactivity, Acene and Molecular systems.
His Antiaromaticity research incorporates themes from Medicinal chemistry, Nucleophilic aromatic substitution, Molecular topology, Computational chemistry and Tetrabutylammonium fluoride.
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