What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Hydrogen
- Catalysis
Gerard Parkin mostly deals with Stereochemistry, Medicinal chemistry, Crystallography, Tris and Inorganic chemistry.
His Stereochemistry research is multidisciplinary, incorporating elements of Cyclopentadienyl complex, Molecule, Alkyl and Covalent radius.
His Medicinal chemistry research integrates issues from Ligand, Reaction rate constant, Dissociation, Hydrogen bond and Addition reaction.
The study incorporates disciplines such as Transition metal and Double bond in addition to Crystallography.
The concepts of his Tris study are interwoven with issues in Reactivity, Nickel and Enzyme.
His Inorganic chemistry research includes themes of Zinc, Zinc hydroxide, Deprotonation and Carbonic anhydrase.
His most cited work include:
- Synthetic analogues relevant to the structure and function of zinc enzymes. (692 citations)
- Agostic interactions in transition metal compounds (670 citations)
- Zinc catalysts for on-demand hydrogen generation and carbon dioxide functionalization. (171 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Stereochemistry, Medicinal chemistry, Crystallography, Ligand and Tris.
His research integrates issues of Derivative, Oxidative addition, Denticity and Molecule in his study of Stereochemistry.
His Medicinal chemistry study integrates concerns from other disciplines, such as Molybdenum, Inorganic chemistry, Reactivity, Alkyl and Organic chemistry.
His study in Crystallography is interdisciplinary in nature, drawing from both Hydride, Metal and Transition metal.
Gerard Parkin works mostly in the field of Ligand, limiting it down to topics relating to Zinc and, in certain cases, Cadmium.
His Tris study incorporates themes from Magnesium, Sulfur, Thallium and Monomer.
He most often published in these fields:
- Stereochemistry (38.40%)
- Medicinal chemistry (34.40%)
- Crystallography (32.00%)
What were the highlights of his more recent work (between 2013-2021)?
- Medicinal chemistry (34.40%)
- Crystallography (32.00%)
- Ligand (26.40%)
In recent papers he was focusing on the following fields of study:
His main research concerns Medicinal chemistry, Crystallography, Ligand, Tris and Stereochemistry.
His Medicinal chemistry research includes elements of Formate, Zinc, Catalysis, Alkyl and Organic chemistry.
His research in Crystallography intersects with topics in Hydride, Tungsten, Characterization, Molecule and Density functional theory.
His Ligand research is multidisciplinary, incorporating perspectives in Pyridine, Bond length, Covalent radius, Inorganic chemistry and Atrane.
His biological study spans a wide range of topics, including Cleavage, Sulfur, Zirconium, Cadmium and Monomer.
Gerard Parkin interconnects Borohydride, Oxidative addition, Dimer and Metal in the investigation of issues within Stereochemistry.
Between 2013 and 2021, his most popular works were:
- Application of the Covalent Bond Classification Method for the Teaching of Inorganic Chemistry (75 citations)
- Dehydrogenation, disproportionation and transfer hydrogenation reactions of formic acid catalyzed by molybdenum hydride compounds (46 citations)
- Zinc and Magnesium Catalysts for the Hydrosilylation of Carbon Dioxide. (43 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Hydrogen
- Catalysis
Gerard Parkin mainly investigates Medicinal chemistry, Ligand, Crystallography, Catalysis and Inorganic chemistry.
His studies in Medicinal chemistry integrate themes in fields like Silane, Zinc, Formate, Photochemistry and Nuclear magnetic resonance spectroscopy.
His work carried out in the field of Ligand brings together such families of science as Tris and Covalent radius.
His Tris research incorporates themes from Metal and Monomer.
His Crystallography study combines topics in areas such as Halide, Molecule and Stereochemistry.
His research investigates the link between Inorganic chemistry and topics such as Hydrogen bond that cross with problems in Magnesium fluoride and Ionic bonding.
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