What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Oxygen
Jean-Michel Léger spends much of his time researching Crystallography, Orthorhombic crystal system, Stereochemistry, Phase and Phase transition.
In the field of Crystallography, his study on Crystal structure overlaps with subjects such as Type.
His study in Crystal structure is interdisciplinary in nature, drawing from both Cubic zirconia and Composite material, Diamond.
His Orthorhombic crystal system research focuses on subjects like Monoclinic crystal system, which are linked to Analytical chemistry.
His Stereochemistry research includes elements of Supramolecular chemistry and Molecular recognition.
His Phase transition study integrates concerns from other disciplines, such as Tetragonal crystal system and Rutile.
His most cited work include:
- Synthesis and Design of Superhard Materials (939 citations)
- X-ray diffraction study of the phase transitions and structural evolution of tin dioxide at high pressure:ffRelationships between structure types and implications for other rutile-type dioxides (212 citations)
- Aromatic δ-Peptides (189 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Crystallography, Stereochemistry, Crystal structure, Phase and Organic chemistry.
Jean-Michel Léger has included themes like Phase transition and Diffraction in his Crystallography study.
His work investigates the relationship between Diffraction and topics such as Bulk modulus that intersect with problems in Valence.
The various areas that Jean-Michel Léger examines in his Stereochemistry study include Chemical synthesis and Helix.
His Crystal structure research is multidisciplinary, incorporating perspectives in Molecule and Medicinal chemistry.
His studies in Phase integrate themes in fields like Ambient pressure and Analytical chemistry.
He most often published in these fields:
- Crystallography (27.59%)
- Stereochemistry (22.99%)
- Crystal structure (19.16%)
What were the highlights of his more recent work (between 2006-2013)?
- Stereochemistry (22.99%)
- Organic chemistry (12.64%)
- Crystallography (27.59%)
In recent papers he was focusing on the following fields of study:
His main research concerns Stereochemistry, Organic chemistry, Crystallography, Combinatorial chemistry and Crystal structure.
His work on Smiles rearrangement as part of general Stereochemistry study is frequently linked to Linker, bridging the gap between disciplines.
Many of his studies on Crystallography apply to Ring as well.
His work deals with themes such as Microwave irradiation, Catalysis, Regioselectivity, Pyrimidine and Chemical synthesis, which intersect with Combinatorial chemistry.
His studies deal with areas such as Intramolecular force, Molecule, Powder diffraction and Phase as well as Crystal structure.
His research in Helix intersects with topics in Folding and Oligomer.
Between 2006 and 2013, his most popular works were:
- Review of different methods for developing nanoelectrocatalysts for the oxidation of organic compounds (127 citations)
- Proteomorphous objects from abiotic backbones. (62 citations)
- New ferrocenic pyrrolo[1,2-a]quinoxaline derivatives: synthesis, and in vitro antimalarial activity--Part II. (62 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Oxygen
Jean-Michel Léger mainly investigates Crystallography, Stereochemistry, Helix, Catalysis and Chemical synthesis.
His work in Crystallography addresses issues such as Oligomer, which are connected to fields such as Supramolecular chemistry and Pyridine.
The study incorporates disciplines such as Molecule and Crystal structure in addition to Pyridine.
His Stereochemistry research is multidisciplinary, incorporating elements of Dimer and Halogenation.
His Catalysis research incorporates themes from Combinatorial chemistry, Electrocatalyst, Electrochemistry and Chemical engineering.
In his research, Moiety, Tertiary amine, Quinoxaline and Piperazine is intimately related to Stereoisomerism, which falls under the overarching field of Chemical synthesis.
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