Description

• Application: Post-synthetic modulation of the charge distribution in a metal–organic framework for optimal binding of carbon dioxide and sulfur dioxide: This study discusses the modulation of pore environment to optimize the binding of sulfur dioxide in metal-organic frameworks. (L Li et al., 2019).Sulfation of abies ethanol lignin by complexes of sulfur trioxide with 1, 4-dioxane and pyridine: Research on the sulfation of lignin using a complex of sulfur trioxide with pyridine, exploring its implications and efficiency. (YN Malyar et al., 2021).Antioxidant and anticoagulant activities of mycelia polysaccharides from Catathelasma ventricosum after sulfated modification: This article explores the use of sulfur trioxide–pyridine complex for sulfating polysaccharides, enhancing their biological activities. (Y Liu et al., 2018).Sulfation of citrus pectin by pyridine-sulfurtrioxide complex and its anticoagulant activity: Study on derivatizing citrus pectin using a pyridine-sulfur trioxide complex to explore its potential health benefits. (Y Hu et al., 2015).Sulfur Dioxide–Pyridine Dimer. FTIR and Theoretical Evidence for a Low-Symmetry Structure: An investigation into the structure of the sulfur dioxide–pyridine complex using FTIR spectroscopy and theoretical models. (JW Keller, 2015).
• Analysis Note: Assay (acidimetric): ≥ 97.0 %Melting range (lower value): ≥ 160 °CMelting range (upper value): ≤ 170 °C