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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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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.

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.
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Preface for Small-Molecule Activation: From Biological Principles to Energy Applications. Part 2: Small Molecules Related to the Global Nitrogen Cycle

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.
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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.
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Electronic Structures of an [Fe(NNR2)]+/0/– Redox Series: Ligand Noninnocence and Implications for Catalytic Nitrogen Fixation

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.