Bio-inspired stabilization of sulfenyl iodide RS-I in a Zr(iv )-based metal–organic framework
Autor: | Ka-Kit Yee, Zhengtao Xu, Yan-Lung Wong |
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Rok vydání: | 2016 |
Předmět: |
Iodide
chemistry.chemical_element Disproportionation Spectrum Analysis Raman 010402 general chemistry Photochemistry Iodine 01 natural sciences Inorganic Chemistry X-Ray Diffraction Spectroscopy Fourier Transform Infrared Polymer chemistry Molecule Dicarboxylic Acids Sulfhydryl Compounds chemistry.chemical_classification 010405 organic chemistry Iodides 0104 chemical sciences Thermogravimetry chemistry Metals X-ray crystallography Thiol Metal-organic framework Zirconium Oxidation-Reduction |
Zdroj: | Dalton Transactions. 45:5334-5338 |
ISSN: | 1477-9234 1477-9226 |
Popis: | A Zr(IV)-based metal-organic framework (MOF) appended with free-standing thiol (-SH) groups was found to react readily with I2 molecules to form sulfenyl iodide (S-I) units. In contrast to its solution chemistry of facile disproportionation into disulfide and I2, the sulfenyl iodide (SI) function, anchored onto the rigid MOF grid and thus prevented from approaching one another to undergo the dismutation reaction, exhibits distinct stability even at elevated temperatures (e.g., 90 °C). On a conceptual plane, this simple and effective solid host also captures the spatial confinement observed for the complex biomacromolecular scaffolds involved in iodine thyroid chemistry, wherein the spatial isolation and consequent stabilization of sulfenyl/selenenyl iodides are exerted by means of the protein scaffolds. |
Databáze: | OpenAIRE |
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