What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Oxygen
His primary areas of study are Stereochemistry, Organic chemistry, Catalysis, Alkyl and Crystallography.
His Stereochemistry research is multidisciplinary, relying on both Thiocyanate, Molybdenum and Stereoisomerism.
His work carried out in the field of Catalysis brings together such families of science as Combinatorial chemistry, Aryl and Ligand.
The study incorporates disciplines such as Inorganic chemistry, Photochemistry and Manganese in addition to Ligand.
His Alkyl study combines topics in areas such as Reactivity, Radical, Medicinal chemistry and Endothermic process.
His Crystallography research includes themes of Acetone, Halogen bond, Hydrogen bond, Halogen and Transition metal.
His most cited work include:
- Structural competition between hydrogen bonds and halogen bonds. (292 citations)
- Manganese Catalysts with Bulky Bipyridine Ligands for the Electrocatalytic Reduction of Carbon Dioxide: Eliminating Dimerization and Altering Catalysis (206 citations)
- Evolution of iridium-based molecular catalysts during water oxidation with ceric ammonium nitrate. (157 citations)
What are the main themes of his work throughout his whole career to date?
Stereochemistry, Medicinal chemistry, Crystallography, Ligand and Photochemistry are his primary areas of study.
His Stereochemistry study combines topics from a wide range of disciplines, such as Aryl and Platinum, Catalysis.
His research in Medicinal chemistry intersects with topics in Reactivity, Organic chemistry, Metal and Phosphine.
Curtis E. Moore has researched Crystallography in several fields, including Inorganic chemistry, Density functional theory and Molecule, Hydrogen bond.
In Ligand, Curtis E. Moore works on issues like Isocyanide, which are connected to Terphenyl.
His studies deal with areas such as Dissociation, Manganese, Bipyridine and Ruthenium as well as Photochemistry.
He most often published in these fields:
- Stereochemistry (29.13%)
- Medicinal chemistry (30.00%)
- Crystallography (26.52%)
What were the highlights of his more recent work (between 2017-2021)?
- Crystallography (26.52%)
- Medicinal chemistry (30.00%)
- Ligand (22.17%)
In recent papers he was focusing on the following fields of study:
Curtis E. Moore focuses on Crystallography, Medicinal chemistry, Ligand, Polymer chemistry and Metal.
His Crystallography research incorporates themes from Proton NMR, Dimer, Hydrogen bond, Isocyanide and Density functional theory.
His Medicinal chemistry research integrates issues from Nitric oxide, Reductive elimination, Synthon and Phosphine.
In his research, Cobalt, Diazoacetamide and Trimethylsilyl is intimately related to Reactivity, which falls under the overarching field of Ligand.
His Polymer chemistry research includes elements of Carotene, Molecule and Phenanthroline.
His Stereochemistry research focuses on Enantioselective synthesis and how it connects with Aryl.
Between 2017 and 2021, his most popular works were:
- Manganese N-Heterocyclic Carbene Pincers for the Electrocatalytic Reduction of Carbon Dioxide (23 citations)
- Covalent attachment of [Ni(alkynyl-cyclam)]2+ catalysts to glassy carbon electrodes. (21 citations)
- Terminal coordination of diatomic boron monofluoride to iron. (17 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Oxygen
His scientific interests lie mostly in Catalysis, Crystallography, Photochemistry, Transition metal and Ligand.
The various areas that Curtis E. Moore examines in his Catalysis study include Combinatorial chemistry and Aryl.
His work deals with themes such as Proton NMR, Halogen bond, Hydrogen bond and Density functional theory, which intersect with Crystallography.
His studies in Photochemistry integrate themes in fields like Ion, Isomerization and Redox active.
His Transition metal study integrates concerns from other disciplines, such as Molecule and Coordination complex.
His study in Ligand is interdisciplinary in nature, drawing from both Cobalt, Steric effects and Polymer chemistry.
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