Issue 14, 2022

Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen

Abstract

Rhenium complexes with aliphatic PNP pincer ligands have been shown to be capable of reductive N2 splitting to nitride complexes. However, the conversion of the resulting nitride to ammonia has not been observed. Here, the thermodynamics and mechanism of the hypothetical N–H bond forming steps are evaluated through the reverse reaction, conversion of ammonia to the nitride complex. Depending on the conditions, treatment of a rhenium(III) precursor with ammonia gives either a bis(amine) complex [(PNP)Re(NH2)2Cl]+, or results in dehydrohalogenation to the rhenium(III) amido complex, (PNP)Re(NH2)Cl. The N–H hydrogen atoms in this amido complex can be abstracted by PCET reagents which implies that they are quite weak. Calorimetric measurements show that the average bond dissociation enthalpy of the two amido N–H bonds is 57 kcal mol−1, while DFT computations indicate a substantially weaker N–H bond of the putative rhenium(IV)-imide intermediate (BDE = 38 kcal mol−1). Our analysis demonstrates that addition of the first H atom to the nitride complex is a thermochemical bottleneck for NH3 generation.

Graphical abstract: Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen

Supplementary files

Article information

Article type
Edge Article
Submitted
15 ágú. 2021
Accepted
22 feb. 2022
First published
04 mar. 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2022,13, 4010-4018

Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen

G. P. Connor, D. Delony, J. E. Weber, B. Q. Mercado, J. B. Curley, S. Schneider, J. M. Mayer and P. L. Holland, Chem. Sci., 2022, 13, 4010 DOI: 10.1039/D1SC04503B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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