Redox-Controlled and Reversible N–N Bond Forming and Splitting with an IronIV Terminal Imido Ligand
Author:
Affiliation:
1. Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States
2. Inorganic Chemistry, Department of Chemistry and Pharmacy, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), 91058 Erlangen, Germany
Funder
Friedrich-Alexander-University Erlangen-N??rnberg (FAU)
DOE BES
The University of Pennsylvania
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.1c01509
Reference52 articles.
1. Ruthenium-catalysed oxidative conversion of ammonia into dinitrogen
2. Cationic Charges Leading to an Inverse Free‐Energy Relationship for N−N Bond Formation by Mn VI Nitrides
3. Decay of Iron(V) Nitride Complexes By a NN Bond-Coupling Reaction in Solution: A Combined Spectroscopic and Theoretical Analysis
4. Substitution-induced nitrogen-nitrogen coupling for nitride coordinated to osmium(VI)
5. Formation of μ-dinitrogen (salen)osmium complexes via ligand-induced N⋯N coupling of (salen)osmium(vi) nitrides
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