# Continuous-flow synthesis of Pd(ii)-anchored amino-functionalised magnetic silica nanoparticles as a robust recyclable catalyst for aqueous Sonogashira cross-coupling

**Authors:** Uthai Sakee, Aekkaphon Mokkarat, Widchaya Radchatawedchakoon, Senee Kruanetr, Ratchaneekorn Pilasombat

PMC · DOI: 10.1039/d6ra01007e · RSC Advances · 2026-03-23

## TL;DR

Researchers developed a reusable magnetic palladium catalyst for efficient chemical reactions in water, offering a sustainable approach to carbon-carbon bond formation.

## Contribution

A scalable continuous-flow method to synthesize a robust, recyclable Pd(ii)-based nanocatalyst for aqueous Sonogashira coupling.

## Key findings

- The catalyst achieved up to 99% yield in coupling reactions with short reaction times.
- It was reused for at least 15 cycles with minimal Pd loss, confirmed by ICP-OES.
- Hammett analysis showed substituent effects on reaction rates, offering mechanistic insights.

## Abstract

A robust and magnetically recoverable palladium nanocatalyst, Fe3O4@SiO2–NH2–Pd(ii), was prepared through a scalable continuous-flow coprecipitation/silanisation strategy and evaluated in Sonogashira cross-coupling reactions in water. Although amino-functionalised magnetic silica supports have been reported, their use as heterogeneous catalysts for aqueous Sonogashira coupling has received comparatively limited attention. Under the optimised conditions, using water as the sole reaction medium, CuI/PPh3 as the cocatalytic system, and triethylamine as the base, a broad range of iodoanilines and terminal alkynes underwent efficient coupling to afford the desired products in up to 99% isolated yield within short reaction times. The catalyst showed excellent durability and was readily recovered by magnetic separation and reused for at least 15 consecutive cycles with minimal palladium loss, as confirmed by ICP-OES analysis. Hot-filtration and recyclability studies indicate that the reaction proceeds predominantly through a heterogeneous pathway, with at most a minor contribution from soluble palladium species. Hammett analysis revealed clear substituent effects on the reaction rate, providing useful mechanistic insight into the catalytic cycle. The combination of continuous-flow synthesis, aqueous-phase catalysis, and magnetic recyclability highlights the practical potential of this nanocatalyst for more sustainable carbon–carbon bond formation.

A robust and magnetically recoverable palladium nanocatalyst, Fe3O4@SiO2–NH2–Pd(ii), was prepared through a scalable continuous-flow coprecipitation/silanisation strategy and evaluated in Sonogashira cross-coupling reactions in water.

## Linked entities

- **Chemicals:** CuI (PubChem CID 104815), PPh3 (PubChem CID 11776), triethylamine (PubChem CID 8471)

## Full-text entities

- **Chemicals:** triethylamine (MESH:C016162), alkynes (MESH:D000480), palladium (MESH:D010165), CuI (MESH:C073870), water (MESH:D014867), silica (MESH:D012822), carbon (MESH:D002244), Fe3O4@SiO2-NH2-Pd(ii) (-)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13007890/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13007890/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC13007890/full.md

---
Source: https://tomesphere.com/paper/PMC13007890