J
Jonas C. Peters
Researcher at California Institute of Technology
Publications - 232
Citations - 28779
Jonas C. Peters is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Catalysis & Ligand. The author has an hindex of 79, co-authored 231 publications receiving 23468 citations. Previous affiliations of Jonas C. Peters include Massachusetts Institute of Technology.
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Journal ArticleDOI
CO Reduction to CH3OSiMe3: Electrophile-Promoted Hydride Migration at a Single Fe Site.
TL;DR: The synthesis of reduced iron-hydride/carbonyl complexes that enable an electrophile-promoted hydride migration process, resulting in the reduction of coordinated CO to a siloxymethyl (LnFe-CH2OSiMe3) group is described.
Posted ContentDOI
Breaking Scaling Relationships in CO2 Reduction on Copper Alloys with Organic Additives.
Yungchieh Lai,Nicholas B. Watkins,Alonso Rosas-Hernández,Arnaud Thevenon,Gavin P. Heim,Lan Zhou,Yueshen Wu,Jonas C. Peters,John M. Gregoire,Theodor Agapie +9 more
TL;DR: In this paper, high-throughput experimentation on 14 bulk copper bimetallic alloys allowed for data-driven identification of a scaling relationship between the partial current densities of methane and C2+ products.
Journal ArticleDOI
Preface for Small-Molecule Activation: From Biological Principles to Energy Applications. Part 2: Small Molecules Related to the Global Nitrogen Cycle
Nicolai Lehnert,Jonas C. Peters +1 more
TL;DR: The nitrogen cycle is among the most significant biogeochemical cycles on Earth because nitrogen is an essential nutrient for all forms of life, and access to fixed forms of nitrogen constitutes in many cases the most limiting factor for plant growth.
Journal ArticleDOI
Photoinduced, Copper-Catalyzed Alkylation of Amides with Unactivated Secondary Alkyl Halides at Room Temperature.
TL;DR: In this article, a photoinduced transition-metal catalyzed N-alkylation of amides with unactivated secondary alkyl halides was developed. But this method is not suitable for the case of nonlinear amides.
Journal ArticleDOI
Electronic Structures of an [Fe(NNR2)]+/0/– Redox Series: Ligand Noninnocence and Implications for Catalytic Nitrogen Fixation
Niklas B. Thompson,Paul H. Oyala,Hai T. Dong,Matthew J. Chalkley,Jiyong Zhao,E. Ercan Alp,Michael Hu,Nicolai Lehnert,Jonas C. Peters +8 more
TL;DR: Evidence is provided suggesting that the present iron complexes are best viewed in terms of an open-shell [NNR2]•- ligand coupled antiferromagnetically to the Fe center, which resembles that of the classically noninnocent ligand NO and may have mechanistic implications for selectivity in N2 fixation activity.