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 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.
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.
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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Synthesis and Design of Superhard Materials
J. Haines;J. M. Leger;G. Bocquillon.
Annual Review of Materials Research (2001)
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
J. Haines;J. M. Léger.
Physical Review B (1997)
Hua Jiang;Jean-Michel Léger;Ivan Huc.
Journal of the American Chemical Society (2003)
Relative stability of ZrO 2 and HfO 2 structural phases
J. E. Lowther;J. K. Dewhurst;J. M. Leger;J. Haines.
Physical Review B (1999)
Pressure-induced structural phase transitions in zirconia under high pressure.
Jean Michel Leger;P.E. Tomaszewski;A. Atouf;Altair Soria Pereira.
Physical Review B (1993)
Review of different methods for developing nanoelectrocatalysts for the oxidation of organic compounds
C. Coutanceau;S. Brimaud;C. Lamy;J.-M. Léger.
Electrochimica Acta (2008)
Pressure Effect on the Curie Temperatures of Transition Metals and Alloys
J. M. Leger;C. Loriers-Susse;B. Vodar.
Physical Review B (1972)
Discovery of hardest known oxide
J. M. Léger;J. Haines;M. Schmidt;J. P. Petitet.
Synthesis, antimalarial activity, and molecular modeling of new pyrrolo[1,2-a]quinoxalines, bispyrrolo[1,2-a]quinoxalines, bispyrido[3,2-e]pyrrolo[1,2-a]pyrazines, and bispyrrolo[1,2-a]thieno[3,2-e]pyrazines
Jean Guillon;Philippe Grellier;Mehdi Labaied;Pascal Sonnet.
Journal of Medicinal Chemistry (2004)
Molecular Apple Peels
Joachim Garric;Jean-Michel Léger;Ivan Huc.
Angewandte Chemie (2005)
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