2005 - Fellow of the Royal Society, United Kingdom
1985 - Fellow of Alfred P. Sloan Foundation
Philip P. Power mainly focuses on Crystallography, Stereochemistry, Crystal structure, Molecule and Inorganic chemistry. He combines subjects such as Terphenyl, X-ray, Tin, Aryl and Monomer with his study of Crystallography. His Stereochemistry research incorporates elements of Alkyne, Ligand, Medicinal chemistry and Lithium.
His biological study spans a wide range of topics, including Yield, Cobalt, Inorganic compound and Dimer. His work in Molecule addresses issues such as Computational chemistry, which are connected to fields such as Molecular orbital and Radical. His Inorganic chemistry research incorporates themes from Ion, Gallium, Hydride and Multiple bonds.
His primary areas of investigation include Crystallography, Stereochemistry, Crystal structure, Medicinal chemistry and Molecule. His Crystallography research includes elements of Inorganic chemistry, Characterization, X-ray, Ligand and Transition metal. His study looks at the intersection of Inorganic chemistry and topics like Tin with Germanium.
His research investigates the link between Stereochemistry and topics such as Terphenyl that cross with problems in Infrared spectroscopy. His study in Crystal structure is interdisciplinary in nature, drawing from both Ether, Inorganic compound and Nuclear magnetic resonance spectroscopy. His research in Medicinal chemistry intersects with topics in Hydride, Organic chemistry, Group, Amide and Photochemistry.
His primary scientific interests are in Crystallography, Stereochemistry, Medicinal chemistry, Terphenyl and Ligand. The Crystallography study combines topics in areas such as Steric effects, Transition metal, Metal, Infrared spectroscopy and Monomer. His Stereochemistry research also works with subjects such as
The various areas that he examines in his Medicinal chemistry study include Hydrogen, Hydride, Moiety, Photochemistry and Tin. His Terphenyl course of study focuses on Aryl and Ring and Chromium. His studies deal with areas such as Isocyanide and Amide as well as Ligand.
Philip P. Power mostly deals with Crystallography, Photochemistry, Medicinal chemistry, Stereochemistry and Molecule. His primary area of study in Crystallography is in the field of Mössbauer spectroscopy. His Photochemistry research is multidisciplinary, incorporating perspectives in Silylene, Moiety and Germanium.
His Medicinal chemistry research integrates issues from Hydrogen, Hydride, Tin, Ammonia and Oxidative addition. Philip P. Power has researched Stereochemistry in several fields, including Reagent, Ligand and Multiple bonds. His studies in Molecule integrate themes in fields like Computational chemistry, Reactivity and Monomer.
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.
π-Bonding and the Lone Pair Effect in Multiple Bonds between Heavier Main Group Elements
Philip P. Power.
Chemical Reviews (1999)
Main-group elements as transition metals
Philip P. Power.
Nature (2010)
π-Bonding and the Lone Pair Effect in Multiple Bonds Involving Heavier Main Group Elements: Developments in the New Millennium
Roland C. Fischer;Philip P. Power.
Chemical Reviews (2010)
Synthesis of a stable compound with fivefold bonding between two chromium(I) centers.
Tailuan Nguyen;Andrew D. Sutton;Marcin Brynda;James C. Fettinger.
Science (2005)
Slow magnetization dynamics in a series of two-coordinate iron(II) complexes
Joseph M. Zadrozny;Mihail Atanasov;Mihail Atanasov;Aimee M. Bryan;Chun Yi Lin.
Chemical Science (2013)
Persistent and stable radicals of the heavier main group elements and related species.
Philip P. Power.
Chemical Reviews (2003)
Facile activation of dihydrogen by an unsaturated heavier main group compound.
Geoffrey H. Spikes;James C. Fettinger;Philip P. Power.
Journal of the American Chemical Society (2005)
The chemistry of boron and its speciation in plants
Philip P. Power;William G. Woods.
Plant and Soil (1997)
Synthesis and Characterization of 2,6-Trip2H3C6PbPbC6H3-2,6-Trip2 (Trip = C6H2-2,4,6-i-Pr3): A Stable Heavier Group 14 Element Analogue of an Alkyne
Lihung Pu;and Brendan Twamley;Philip P. Power.
Journal of the American Chemical Society (2000)
Metal Amide Chemistry
Michael Lappert;Andrey Protchenko;Philip Power;Alexandra Seeber.
(2009)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of California, Davis
University of California, Davis
Syracuse University
University of Sussex
Missouri University of Science and Technology
The University of Texas at Arlington
Fukui Institute for Fundamental Chemistry
Missouri University of Science and Technology
University of Idaho
Southern University of Science and Technology
University of Siegen
Humboldt-Universität zu Berlin
Georgia Institute of Technology
Glenn Research Center
Kettering University
North Carolina State University
Stellenbosch University
National Institute of Chemical Physics and Biophysics
Hospital General Universitario Gregorio Marañón
Cornell University
University of Cambridge
University of California, Berkeley
University of Oxford
Science.org
Cato Institute
Humboldt-Universität zu Berlin