# Reducing undesired solubility of squarephaneic tetraimide for use as an organic battery electrode material

**Authors:** Bowen Ding, Manik Bhosale, Troy L. R. Bennett, Martin Heeney, Felix Plasser, Birgit Esser, Florian Glöcklhofer

PMC · DOI: 10.1039/d3fd00145h · Faraday Discussions · 2023-08-17

## TL;DR

A new unsubstituted squarephaneic tetraimide material with reduced solubility is developed and tested as a potential organic battery electrode.

## Contribution

The novel unsubstituted derivative SqTI-H is synthesized with reduced solubility and improved thermal stability for battery applications.

## Key findings

- SqTI-H exhibits low neutral state solubility in organic solvents due to hydrogen-bonding capabilities.
- Reversible electrochemical reduction of SqTI-H to the dianion state was observed at −1.25 V vs. Fc/Fc+.
- Preliminary battery testing showed imperfect cycling performance, likely due to solubility of reduced states.

## Abstract

Locally aromatic alkyl-N-substituted squarephaneic tetraimide (SqTI) conjugated macrocycles are four-electron reducible, owing to global aromaticity and presumed global Baird aromaticity of the dianion and tetraanion states, respectively. However, their good solubility inhibits their application as a battery electrode material. By applying sidechain removal as a strategy to reduce SqTI solubility, we report the development of its unsubstituted derivative SqTI-H, which was obtained directly from squarephaneic tetraanhydride by facile treatment with hexamethyldisilazane and MeOH. Compared to alkyl-N-substituted SqTI-Rs, SqTI-H exhibited further improved thermal stability and low neutral state solubility in most common organic solvents, owing to computationally demonstrated hydrogen-bonding capabilities emanating from each imide position on SqTI-H. Reversible solid state electrochemical reduction of SqTI-H to the globally aromatic dianion state was also observed at −1.25 V vs. Fc/Fc+, which could be further reduced in two stages. Preliminary testing of SqTI-H in composite electrodes for lithium–organic half cells uncovered imperfect cycling performance, which may be explained by persistent solubility of reduced states, necessitating further optimisation of electrode fabrication procedures to attain maximum performance.

Unsubstituted squarephaneic tetraimide with reduced solubility due to H-bonding interactions is synthesised, characterised, and tested as a battery electrode material.

## Linked entities

- **Chemicals:** hexamethyldisilazane (PubChem CID 13838), MeOH (PubChem CID 887)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10926975/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC10926975/full.md

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Source: https://tomesphere.com/paper/PMC10926975