What is she best known for?
The fields of study she is best known for:
- Organic chemistry
- Catalysis
- Hydrogen
Odile Eisenstein mostly deals with Stereochemistry, Crystallography, Medicinal chemistry, Catalysis and Ligand.
The concepts of her Stereochemistry study are interwoven with issues in Metathesis, Molecule, Crystal structure and Carbene.
Her Crystallography research includes elements of Metal, Agostic interaction, Photochemistry, Singlet state and Hydrogen bond.
Her Medicinal chemistry research is multidisciplinary, incorporating perspectives in Chemical bond, Fluorine, Oxidative addition, Double bond and Reaction mechanism.
Her work on Iridium as part of general Catalysis study is frequently connected to Oxidation reduction, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Her Ligand study combines topics from a wide range of disciplines, such as Counterion, Outer sphere electron transfer and Phosphine.
Her most cited work include:
- C-H bond activation in transition metal species from a computational perspective (715 citations)
- A new intermolecular interaction: unconventional hydrogen bonds with element-hydride bonds as proton acceptor. (464 citations)
- Highly Active and Robust Cp* Iridium Complexes for Catalytic Water Oxidation (456 citations)
What are the main themes of her work throughout her whole career to date?
Odile Eisenstein mainly focuses on Crystallography, Stereochemistry, Medicinal chemistry, Photochemistry and Computational chemistry.
Odile Eisenstein interconnects Ligand, Transition metal, Molecule, Molecular orbital and Metal in the investigation of issues within Crystallography.
Her work in Stereochemistry addresses subjects such as Extended Hückel method, which are connected to disciplines such as Inorganic compound.
Her study looks at the relationship between Medicinal chemistry and topics such as Catalysis, which overlap with Metathesis.
Her Photochemistry research is multidisciplinary, relying on both Polymer chemistry, Agostic interaction and Ruthenium.
Her Computational chemistry study combines topics in areas such as Ab initio, Reactivity and Lanthanide.
She most often published in these fields:
- Crystallography (40.05%)
- Stereochemistry (32.09%)
- Medicinal chemistry (24.88%)
What were the highlights of her more recent work (between 2011-2020)?
- Catalysis (16.92%)
- Medicinal chemistry (24.88%)
- Crystallography (40.05%)
In recent papers she was focusing on the following fields of study:
Her primary scientific interests are in Catalysis, Medicinal chemistry, Crystallography, Photochemistry and Reactivity.
Her Catalysis study integrates concerns from other disciplines, such as Alkyne metathesis and Metathesis.
Her Medicinal chemistry research incorporates elements of Yield, Hydride, Aniline, Stereochemistry and Cationic polymerization.
Odile Eisenstein has researched Crystallography in several fields, including Ligand, Molecular orbital, Carbon-13 NMR, Density functional theory and Chemical shift.
Her research in Photochemistry intersects with topics in Surface modification, Alkyne, Alkoxide, Intramolecular force and Isomerization.
The Reactivity study combines topics in areas such as Ruthenium, Lewis acids and bases, Silylene, Computational chemistry and Deprotonation.
Between 2011 and 2020, her most popular works were:
- Linear-Selective Hydroarylation of Unactivated Terminal and Internal Olefins with Trifluoromethyl-Substituted Arenes (130 citations)
- Outer sphere hydrogenation catalysis (111 citations)
- Selectivity of C–H Activation and Competition between C–H and C–F Bond Activation at Fluorocarbons (99 citations)
In her most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Hydrogen
Crystallography, Photochemistry, Catalysis, Organic chemistry and Chemical shift are her primary areas of study.
Her work deals with themes such as Ligand and Carbon-13 NMR, which intersect with Crystallography.
Her Photochemistry research is multidisciplinary, incorporating elements of Bifunctional catalyst, Alkyne, Kinetic isotope effect and Reaction mechanism.
Her work in Catalysis is not limited to one particular discipline; it also encompasses Medicinal chemistry.
Her studies deal with areas such as Aryl, Stereochemistry and Trigonal bipyramidal molecular geometry as well as Alkene.
Her research integrates issues of Trifluoromethyl and Reductive elimination in her study of Stereochemistry.
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