What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Hydrogen
His primary scientific interests are in Ligand, Stereochemistry, Catalysis, Medicinal chemistry and Crystallography.
The study incorporates disciplines such as Electronic structure, Transition metal, Alkyl and Electron transfer in addition to Ligand.
His biological study spans a wide range of topics, including Alkylation, Ring, Molecule, Derivative and Deprotonation.
His Catalysis study results in a more complete grasp of Organic chemistry.
His Medicinal chemistry study combines topics in areas such as Olefin fiber, Hydride, Diimine and Imine.
His work on Crystal structure as part of general Crystallography research is frequently linked to Paramagnetism, bridging the gap between disciplines.
His most cited work include:
- Palladium-Catalyzed Alternating Copolymerization of Alkenes and Carbon Monoxide. (672 citations)
- Ligand-centred reactivity in diiminepyridine complexes. (182 citations)
- Efficient palladium catalysts for the carbonylation of alkynes (175 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Medicinal chemistry, Catalysis, Stereochemistry, Crystallography and Ligand.
The Medicinal chemistry study combines topics in areas such as Photochemistry, Aryl, Alkyl and Rhodium.
He has included themes like Polymerization and Monomer in his Catalysis study.
His research in Stereochemistry intersects with topics in Ring and Deprotonation.
In his work, Computational chemistry and Inorganic chemistry is strongly intertwined with Molecule, which is a subfield of Crystallography.
His Ligand research is multidisciplinary, incorporating elements of Alkylation, Metal, Reactivity and Imine.
He most often published in these fields:
- Medicinal chemistry (28.34%)
- Catalysis (25.51%)
- Stereochemistry (24.29%)
What were the highlights of his more recent work (between 2016-2021)?
- Catalysis (25.51%)
- Polymer chemistry (19.03%)
- Medicinal chemistry (28.34%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Catalysis, Polymer chemistry, Medicinal chemistry, Polymerization and Zirconium.
His Catalysis research incorporates themes from Combinatorial chemistry, Photochemistry and Dispersion.
His Polymer chemistry research integrates issues from Methylaluminoxane, Chemical equilibrium, Olefin polymerization, Chain transfer and Isocyanide.
His Medicinal chemistry research incorporates elements of Pincer movement, Halide, Alkene, Oxidative addition and Phosphine.
His research on Polymerization often connects related topics like Cationic polymerization.
In Alkylation, Peter H. M. Budzelaar works on issues like Ligand, which are connected to Pyridine.
Between 2016 and 2021, his most popular works were:
- Accurate Prediction of Copolymerization Statistics in Molecular Olefin Polymerization Catalysis: The Role of Entropic, Electronic, and Steric Effects in Catalyst Comonomer Affinity (28 citations)
- Gold(III) Alkyne Complexes: Bonding and Reaction Pathways. (27 citations)
- Connection of Stereoselectivity, Regioselectivity, and Molecular Weight Capability in rac-R'2Si(2-Me-4-R-indenyl)2ZrCl2 Type Catalysts (20 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Hydrogen
The scientist’s investigation covers issues in Catalysis, Photochemistry, Medicinal chemistry, Steric effects and Polymerization.
His study in Catalysis is interdisciplinary in nature, drawing from both Metallocene, Toluene and Combinatorial chemistry.
He combines subjects such as Homolysis, Solvent and Monomer with his study of Photochemistry.
His biological study spans a wide range of topics, including Aryl, Pincer movement, Radical and Phosphine.
The various areas that Peter H. M. Budzelaar examines in his Phosphine study include Methoxide, Benzene, Stereochemistry and Alkoxide.
Peter H. M. Budzelaar has researched Polymerization in several fields, including Polymer chemistry, Lewis acids and bases and Free phenol.
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