Search results

Search for "sequestrants" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Insoluble methylene-bridged glycoluril dimers as sequestrants for dyes

  • Suvenika Perera,
  • Peter Y. Zavalij and
  • Lyle Isaacs

Beilstein J. Org. Chem. 2025, 21, 2302–2314, doi:10.3762/bjoc.21.176

Graphical Abstract
  • 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. Keywords: cucurbituril; dyes; sequestrants; X-ray crystallography; Introduction The needs of a growing world population and the demands of modern life has resulted in the increased production of both known and new chemical substances including building materials, vitamins and
PDF
Album
Supp Info
Full Research Paper
Published 29 Oct 2025

Cyclodextrins as building blocks for new materials

  • Miriana Kfoury and
  • Sophie Fourmentin

Beilstein J. Org. Chem. 2023, 19, 889–891, doi:10.3762/bjoc.19.66

Graphical Abstract
  • solubilizers, stabilizers, permeation enhancers, cryoprotectors, sequestrants of toxic compounds, taste and odor maskers, coating materials of solid surfaces, and chiral receptors has been successfully explored in food, packaging, cosmetics, textiles, separation processes, environmental remediation, extraction
PDF
Editorial
Published 19 Jun 2023
Other Beilstein-Institut Open Science Activities