# Theoretical Investigation of the Pyridinium-Inspired Catalytic Dehydration of Heptafluoro-Iso-Butyramide for the Synthesis of Environmentally Friendly Insulating Gas Heptafluoro-Iso-Butyronitrile

**Authors:** Jiageng Xiong, Hua Hou, Baoshan Wang

PMC · DOI: 10.3390/molecules29163952 · Molecules · 2024-08-21

## TL;DR

This paper explores a new eco-friendly method to produce an insulating gas using a catalyst system, offering a sustainable alternative to a harmful greenhouse gas.

## Contribution

The study reveals a synergistic catalytic mechanism involving TFAA and Py for efficient gas synthesis.

## Key findings

- TFAA catalyzes the dehydration of heptafluoro-iso-butyramide to produce the eco-friendly gas.
- Pyridine lowers the energy barrier of the rate-determining step by forming pyridinium hydrogen.
- The TFAA/Py co-catalyst reduces the Gibbs free energy barrier by over 40 kcal/mol.

## Abstract

Heptafluoro-iso-butyronitrile (i-C3F7CN) represents a feasible eco-friendly replacement gas for the most potent greenhouse gas sulfur hexafluoride in various high-voltage power transmission equipment. The reaction mechanisms for the in situ synthesis of i-C3F7CN from heptafluoro-iso-butyramide [i-C3F7C(O)NH2] in the presence of trifluoroacetic anhydride (TFAA) and pyridine (Py) in dimethylformamide solution have been studied within density functional theory with M06-2X exchange–correlation functional with the 6-311++G(d,p) basis set and the high-level ab initio complete basis set quadratic CBS-QB3 method. It is revealed that the unimolecular dehydration of i-C3F7C(O)NH2 can be catalyzed efficiently by TFAA in terms of both kinetic and thermodynamic aspects, producing i-C3F7CN and trifluoroacetic acid (TFA). Furthermore, Py is capable of reducing the energy barrier of the rate-determining step through hydrogen abstraction to form pyridinium hydrogen. The synergic effect of the TFAA/Py co-catalyst plays a pivotal role in the production of i-C3F7CN as the Gibbs free energy barrier can be lowered by more than 40 kcal/mol with the ratio of TFAA:2Py, in accordance with the experimental observation. The present theoretical work provides new insights into the rational design on the novel catalysts for large-scale synthesis of the perfluorinated nitriles.

## Linked entities

- **Chemicals:** heptafluoro-iso-butyronitrile (PubChem CID 12633773), trifluoroacetic anhydride (PubChem CID 9845), pyridine (PubChem CID 1049), dimethylformamide (PubChem CID 6228), trifluoroacetic acid (PubChem CID 6422), sulfur hexafluoride (PubChem CID 17358)

## Full-text entities

- **Chemicals:** hydrogen (MESH:D006859), dimethylformamide (MESH:D004126), Heptafluoro-iso-butyronitrile (-), Py (MESH:C023666), TFA (MESH:D014269), TFAA (MESH:C017958), sulfur hexafluoride (MESH:D013459)

## Full text

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## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11357488/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC11357488/full.md

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Source: https://tomesphere.com/paper/PMC11357488