1983 - Fellow of Alfred P. Sloan Foundation
His research on Hydrogen is centered around Hydride and Hydrogenase. His Ion studies intersect with other disciplines such as Protonation, Hydride and Stereochemistry. He integrates many fields, such as Protonation and Ion, in his works. In his papers, he integrates diverse fields, such as Stereochemistry and Hydrogen. In his research, Thomas B. Rauchfuss performs multidisciplinary study on Organic chemistry and Combinatorial chemistry. Thomas B. Rauchfuss performs multidisciplinary study in Combinatorial chemistry and Organic chemistry in his work. Thomas B. Rauchfuss combines Medicinal chemistry and Inorganic chemistry in his research. Thomas B. Rauchfuss performs multidisciplinary study in the fields of Inorganic chemistry and Medicinal chemistry via his papers. While working in this field, Thomas B. Rauchfuss studies both Crystallography and Crystal structure.
Protonation and Stereochemistry are fields of study that intersect with his Ion research. Thomas B. Rauchfuss integrates several fields in his works, including Stereochemistry and Ion. Thomas B. Rauchfuss performs multidisciplinary study on Organic chemistry and Physical chemistry in his works. He integrates Physical chemistry with Organic chemistry in his study. Crystallography and Crystal structure are two areas of study in which he engages in interdisciplinary research. In his research, Thomas B. Rauchfuss undertakes multidisciplinary study on Crystal structure and Crystallography. He performs integrative study on Biochemistry and Receptor. In his research, Thomas B. Rauchfuss performs multidisciplinary study on Receptor and Ligand (biochemistry). His research is interdisciplinary, bridging the disciplines of Biochemistry and Ligand (biochemistry).
His Catalysis research is covered under the topics of Hydrogenase, Catalytic cycle and Active site. His study on Stereochemistry is mostly dedicated to connecting different topics, such as Steric effects and Moiety. He conducts interdisciplinary study in the fields of Steric effects and Catalysis through his works. His research on Moiety frequently connects to adjacent areas such as Stereochemistry. His research on Hydrogenase, Biosynthesis, Cofactor and Active site is centered around Enzyme. Thomas B. Rauchfuss conducted interdisciplinary study in his works that combined Biosynthesis and Enzyme. Thomas B. Rauchfuss combines topics linked to Amine gas treating with his work on Organic chemistry. Borrowing concepts from Crystal structure, Thomas B. Rauchfuss weaves in ideas under Crystallography. The study of Crystal structure is intertwined with the study of Octahedron in a number of ways.
Thomas B. Rauchfuss interconnects Hydrogenase, Catalytic cycle, Catalysis, Heterolysis and Hydride, Metal in the investigation of issues within Moiety. He undertakes multidisciplinary investigations into Catalysis and Turnover number in his work. His research is interdisciplinary, bridging the disciplines of Hydride and Metal. His Stereochemistry study frequently intersects with other fields, such as Moiety and Synthon. Synthon is closely attributed to Stereochemistry in his work. His Enzyme study is focused on Turnover number and Hydrogenase. While working on this project, he studies both Organic chemistry and Combinatorial chemistry. By researching both Combinatorial chemistry and Organic chemistry, Thomas B. Rauchfuss produces research that crosses academic boundaries. Thomas B. Rauchfuss performs multidisciplinary study in the fields of Photochemistry and Enzyme via his papers.
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Frontiers, Opportunities, and Challenges in Biochemical and Chemical Catalysis of CO2 Fixation
Aaron M. Appel;John E. Bercaw;Andrew B. Bocarsly;Holger Dobbek.
Chemical Reviews (2013)
Small molecule mimics of hydrogenases: hydrides and redox
Frédéric Gloaguen;Thomas B. Rauchfuss.
Chemical Society Reviews (2009)
Biomimetic hydrogen evolution catalyzed by an iron carbonyl thiolate.
Frédéric Gloaguen;Joshua D. Lawrence;Thomas B. Rauchfuss.
Journal of the American Chemical Society (2001)
Efficient Production of the Liquid Fuel 2,5-Dimethylfuran from Fructose Using Formic Acid as a Reagent†
Todsapon Thananatthanachon;Thomas B. Rauchfuss.
Angewandte Chemie (2010)
Metal complexes of hemilabile ligands. Reactivity and structure of dichlorobis(o-(diphenylphosphino)anisole)ruthenium(II)
J. C. Jeffrey;T. B. Rauchfuss.
Inorganic Chemistry (1979)
Hydrogenase Enzymes and Their Synthetic Models: The Role of Metal Hydrides.
David Schilter;James M. Camara;Mioy T. Huynh;Sharon Hammes-Schiffer.
Chemical Reviews (2016)
Iron carbonyl sulfides, formaldehyde, and amines condense to give the proposed azadithiolate cofactor of the Fe-only hydrogenases.
Hongxiang Li;Thomas B Rauchfuss.
Journal of the American Chemical Society (2002)
Diiron Azadithiolates as Models for the Iron‐Only Hydrogenase Active Site: Synthesis, Structure, and Stereoelectronics
Joshua D. Lawrence;Hongxiang Li;Thomas B. Rauchfuss;Marc Bénard.
Angewandte Chemie (2001)
Combining acid–base, redox and substrate binding functionalities to give a complete model for the [FeFe]-hydrogenase
James M. Camara;Thomas B. Rauchfuss.
Nature Chemistry (2012)
Synthetic and structural studies on [Fe2(SR)2(CN)x(CO)6-x](x-) as active site models for Fe-only hydrogenases.
Frédéric Gloaguen;Joshua D. Lawrence;Michael Schmidt;Scott R. Wilson.
Journal of the American Chemical Society (2001)
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