What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Molecule
- Nanotechnology
The scientist’s investigation covers issues in Nanotechnology, Supramolecular chemistry, Rotaxane, Stereochemistry and Catenane.
His Nanotechnology study incorporates themes from Molecule, Molecular switch and Bistability.
His research in Supramolecular chemistry intersects with topics in Self-assembly, Non-covalent interactions and Molecular recognition.
J. Fraser Stoddart has included themes like Photochemistry, Monolayer and Polymer chemistry in his Rotaxane study.
His work in Stereochemistry tackles topics such as Crystallography which are related to areas like Ring, Tetrathiafulvalene, Electrochemistry and Metal-organic framework.
His study in Catenane is interdisciplinary in nature, drawing from both Mechanical bond, Redox and Mechanically interlocked molecular architectures.
His most cited work include:
- Artificial Molecular Machines. (1746 citations)
- Dynamic covalent chemistry. (1505 citations)
- Self‐Assembly in Natural and Unnatural Systems (1421 citations)
What are the main themes of his work throughout his whole career to date?
J. Fraser Stoddart focuses on Stereochemistry, Crystallography, Supramolecular chemistry, Nanotechnology and Molecule.
His research integrates issues of Polymer chemistry, Cyclophane, Catenane and Rotaxane in his study of Stereochemistry.
His Crystallography research integrates issues from Proton NMR, Ring, Hydrogen bond and Tetrathiafulvalene.
J. Fraser Stoddart has researched Supramolecular chemistry in several fields, including Molecular recognition, Crown ether, Self-assembly, Stacking and Combinatorial chemistry.
The concepts of his Nanotechnology study are interwoven with issues in Molecular switch, Molecular electronics and Mechanically interlocked molecular architectures.
Molecule is closely attributed to Chemical physics in his research.
He most often published in these fields:
- Stereochemistry (29.18%)
- Crystallography (33.73%)
- Supramolecular chemistry (31.86%)
What were the highlights of his more recent work (between 2015-2021)?
- Supramolecular chemistry (31.86%)
- Crystallography (33.73%)
- Molecule (26.71%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Supramolecular chemistry, Crystallography, Molecule, Nanotechnology and Cyclophane.
His biological study deals with issues like Porosity, which deal with fields such as Hydrogen.
His Crystallography study combines topics in areas such as Viologen, Cage, Radical ion, Ring and Intermolecular force.
As a part of the same scientific study, J. Fraser Stoddart usually deals with the Molecule, concentrating on Redox and frequently concerns with Polymer.
He is interested in Molecular machine, which is a field of Nanotechnology.
His Cyclophane study integrates concerns from other disciplines, such as Combinatorial chemistry, Photochemistry and Perylene.
Between 2015 and 2021, his most popular works were:
- Mechanically Interlocked Molecules (MIMs)-Molecular Shuttles, Switches, and Machines (Nobel Lecture). (302 citations)
- Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes (258 citations)
- The Nature of the Mechanical Bond: From Molecules to Machines (152 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Molecule
- Catalysis
His primary areas of study are Molecule, Supramolecular chemistry, Nanotechnology, Crystallography and Metal-organic framework.
His Molecule research is multidisciplinary, relying on both Chemical physics, Redox and Pyridinium.
His Supramolecular chemistry research includes elements of Topology, Translational symmetry, Diradical and Triptycene.
Molecular machine is the focus of his Nanotechnology research.
His studies in Crystallography integrate themes in fields like Covalent bond, Cationic polymerization, Stereochemistry and Viologen.
His Metal-organic framework study incorporates themes from Porosity, Chemical engineering, Mesoporous material and Cyclodextrin.
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