# On the Facile Synthesis of Triazaarsoles Using Acyclic Precursors

**Authors:** Lilian S. Szych, Daniel S. Frost, Moritz J. Ernst, Jonas Bresien, Manuela Weber, Annelie Puhlmann, Luise Sander, Christian Müller

PMC · DOI: 10.1002/chem.202500514 · Chemistry (Weinheim an Der Bergstrasse, Germany) · 2025-04-07

## TL;DR

This paper presents a new method to synthesize triazaarsoles, which are arsenic-based compounds with potential for further chemical exploration.

## Contribution

The paper introduces a facile synthesis route for rarely explored triazaarsoles using acyclic precursors.

## Key findings

- Dichloroarsanes are effective precursors for synthesizing triazaarsoles.
- DFT calculations show that triazaarsoles exhibit a high degree of aromaticity.
- The method opens the door for studying a wide range of new arsenic-containing heterocycles.

## Abstract

Easily accessible dichloroarsanes are suitable precursors for the synthesis of rarely explored triazaarsoles, the arsenic analogues of tetrazoles and triazaphospholes. Calculations on the DFT level gave insight into the electronic structure of such planar compounds, indicating a high degree of aromaticity. Our preliminary investigations pave the way for accessing and investigating a whole variety of new heterocycles that contain a low‐coordinated arsenic atom.

Easily accessible dichloroarsanes are suitable precursors for the synthesis of novel triazaarsoles, the arsenic analogues of tetrazoles and triazaphospholes. Our findings pave the way to access and fully investigate such aromatic arsenic heterocycles in detail.

## Full-text entities

- **Chemicals:** Triazaarsoles (-), tetrazoles (MESH:D013777), arsenic (MESH:D001151)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12080306/full.md

## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC12080306/full.md

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Source: https://tomesphere.com/paper/PMC12080306