# Insoluble methylene-bridged glycoluril dimers as sequestrants for dyes

## TL;DR

This paper introduces new insoluble compounds that can remove dyes from water, with one variant showing particularly high efficiency.

## Contribution

The study introduces methylene-bridged glycoluril dimers as novel dye sequestrants and compares their performance.

## Key findings

- Catechol-walled H2 outperformed other dimers in dye removal efficiency.
- OMe groups in G2W1–G2W4 reduced their sequestration abilities.
- H2 achieved 94% removal of methylene blue within 10 minutes.

## Abstract

Contamination of water bodies by micropollutants including industrial dyes is a worldwide health and environmental concern. We report the design, synthesis, and characterization of a series of methylene-bridged glycoluril dimers G2W1–G2W4 that are insoluble in water and that differ in the nature of their aromatic sidewalls (G2W4: benzene, G2W3: naphthalene, G2W1 and G2W2: triphenylene). We tested G2W1–G2W4 along with comparator H2 as solid-state sequestrants for a panel of five dyes (methylene blue, methylene violet, acridine orange, rhodamine 6G, and methyl violet 6B). We find that catechol-walled H2 (OH substituents) is a superior sequestrant compared to G2W1–G2W4 (OMe substituents). X-ray crystal structures for G2W1 and G2W3 suggest that the OMe groups fill their own cavity and thereby decrease their abilities as sequestrants. H2 achieved a removal efficiency of 94% for methylene blue whereas G2W1 demonstrated a 64% removal efficiency for methylene violet; both sequestration processes were largely complete within 10 minutes.