Work

Insoluble methylene-bridged glycoluril dimers as sequestrants for dyes

Year: 2025

Type: article

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.

Source: Beilstein Journal of Organic Chemistry

DOI: 10.3762/bjoc.21.176

Authors: Suvenika Perera, Peter Y Zavalij, Lyle Isaacs

Institution: University of Maryland, College Park

Language: English

Topic: Supramolecular Chemistry and Complexes

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

SDGs: Clean water and sanitation, Responsible consumption and production

Open Access status: diamond

Funders: National Science Foundation, University of Maryland, National Institutes of Health, National Institute of General Medical Sciences