What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Hydrogen
Darrin S. Richeson focuses on Stereochemistry, Ligand, Catalysis, Medicinal chemistry and Yield.
His work on Steric effects as part of general Stereochemistry study is frequently linked to Monomer and X-ray crystallography, therefore connecting diverse disciplines of science.
The various areas that Darrin S. Richeson examines in his Ligand study include Crystallography, Photochemistry and Metal.
The Denticity research he does as part of his general Crystallography study is frequently linked to other disciplines of science, such as Magnetization, therefore creating a link between diverse domains of science.
His Catalysis research includes elements of Aryl and Group.
His research in Yield intersects with topics in Titanium and Isocyanide.
His most cited work include:
- EFFECT OF CU-O LAYER SPACING ON THE MAGNETIC FIELD INDUCED RESISTIVE BROADENING OF HIGH-TEMPERATURE SUPERCONDUCTORS (253 citations)
- Single-molecule magnet behavior with a single metal center enhanced through peripheral ligand modifications. (251 citations)
- Constructing a stable carbene with a novel topology and electronic framework (171 citations)
What are the main themes of his work throughout his whole career to date?
Darrin S. Richeson mainly focuses on Stereochemistry, Ligand, Crystallography, Medicinal chemistry and Metal.
His Stereochemistry study combines topics from a wide range of disciplines, such as Yield and Pyridine ligand.
His Ligand study combines topics in areas such as Chelation, Pyridine, Protonation and Coordination geometry.
The concepts of his Crystallography study are interwoven with issues in Lone pair, Transition metal and Hydrogen bond.
His Medicinal chemistry research incorporates themes from Reactivity, Organic chemistry, Catalysis, Coupling reaction and Aryl.
His biological study spans a wide range of topics, including Inorganic chemistry, Ion and Covalent bond.
He most often published in these fields:
- Stereochemistry (34.71%)
- Ligand (31.40%)
- Crystallography (29.75%)
What were the highlights of his more recent work (between 2014-2019)?
- Ligand (31.40%)
- Catalysis (14.88%)
- Crystallography (29.75%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Ligand, Catalysis, Crystallography, Pyridine and Stereochemistry.
His Ligand research incorporates elements of Bimetallic strip, Metal and Polymer chemistry.
The study incorporates disciplines such as Inorganic chemistry, Photochemistry and Acetonitrile in addition to Catalysis.
In general Crystallography study, his work on Single crystal often relates to the realm of Context, thereby connecting several areas of interest.
His Pyridine research integrates issues from Denticity, Steric effects, Transition metal, Coordination complex and Thioether.
His Stereochemistry study incorporates themes from Salt, Supramolecular chemistry, Phthalate and Medicinal chemistry.
Between 2014 and 2019, his most popular works were:
- Electrocatalytic reduction of CO2 using Mn complexes with unconventional coordination environments (27 citations)
- New Experimental Insight into the Nature of Metal-Metal Bonds in Digallium Compounds: J Coupling between Quadrupolar Nuclei. (10 citations)
- Capturing Re(i) in an neutral N,N,N pincer Scaffold and resulting enhanced absorption of visible light. (10 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Hydrogen
- Catalysis
Ligand, Pincer movement, Crystallography, Stereochemistry and Medicinal chemistry are his primary areas of study.
His research in Ligand is mostly concerned with Pincer ligand.
His study in Pincer movement is interdisciplinary in nature, drawing from both Denticity, Pyridine and Single crystal.
His studies in Crystallography integrate themes in fields like Atomic orbital, Nuclear magnetic resonance spectroscopy, J-coupling and Gallium.
His Stereochemistry research is multidisciplinary, incorporating elements of Halide, Metal and Substitution reaction.
His Medicinal chemistry research includes elements of Thioether, Organic chemistry, Catalysis and Epoxide.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
