30899-62-8 Purity
96%
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Specification
A mixed-matrix polyimide membrane was prepared through a non-solvent-induced phase inversion process, containing Cu(II)BTC, Cu(I/II)BTC, and Cu(I) 1,2-ethanedisulfonic acid (EDS) (Cu(I)EDS) metal-organic frameworks (MOFs). The prepared membrane has solvent resistance and mechanical stability and can be used for nanofiltration separation of toluene and n-heptane.
Direct synthesis of Cu(I)EDS
· First, a mixture of copper acetate monohydrate (270 mg, 1.35 mmol), 1,2-ethanedisulfonic acid (EDS, 290 mg, 1.52 mmol), and 4,4' bipyridine (210 mg, 1.34 mmol) was prepared in 10 mL of water.
· The solution was stirred at room temperature for 30 minutes before being transferred to a Teflon cell. The cell was sealed and placed in a stainless-steel reactor, which was then inserted into a preheated sand bath at 150 °C. After four days of reaction, the reactor was allowed to cool down naturally.
· The pH of the solution decreased from 4.2 to 3.1 during the reaction. The resulting yellow-brown crystals were filtered, washed with a mixture of water and acetone two to three times, and finally dried overnight in a vacuum oven.
Silver(I) coordination polymers (CPs) have been widely used in conductive materials, antibacterial agents, luminescent materials and supramolecular chirality due to their structural diversity and rich physical and chemical properties. A cationic silver-based quinoxaline coordination polymer, [Ag(quinoxaline)+][- O3SCH2CH2SO3-]0.5·H2O (SLUG-37) , has been successfully developed with strong white light emission, showing potential for use as a white light LED. 1,2-Ethanesulfonic acid dihydrate is one of the important raw materials for the synthesis of SLUG-37.
Synthesis of SLUG-37
· AgCH3CO2 (0.17 g, 1.0 mmol), quinoxaline (0.17 g, 1.3 mmol), and either 1,2-ethanedisulfonate disodium salt (0.23 g, 1.0 mmol) or 1,2-ethanedisulfonic acid dihydrate (0.19 g, 1.0 mmol) were dissolved in deionized water (10 mL) in ratios of 1.0:1.3:1.0:400, respectively.
· The solution was stirred at room temperature for 15 minutes before being transferred to a 15 mL Teflon-lined autoclave filled to 2/3 capacity. The autoclave was heated in an oven at temperatures ranging from 100 to 150 °C for 1 to 5 days to complete the reaction.
· An alternative method for synthesizing SLUG-37 involved refluxing or stirring at room temperature using the same reactant ratios, with the crystals filtered after approximately 1 hour of refluxing at 70 °C or 1 day of stirring at room temperature.
The molecular formula of 1,2-Ethanedisulfonic acid dihydrate is C2H10O8S2.
Some synonyms for 1,2-Ethanedisulfonic acid dihydrate are ethane-1,2-disulfonic acid dihydrate and ethylenedisulfonic acid (dihydrate).
The molecular weight of 1,2-Ethanedisulfonic acid dihydrate is 226.2 g/mol.
The parent compound of 1,2-Ethanedisulfonic acid dihydrate is 1,2-Ethanedisulfonic acid.
The IUPAC name of 1,2-Ethanedisulfonic acid dihydrate is ethane-1,2-disulfonic acid;dihydrate.
The InChI of 1,2-Ethanedisulfonic acid dihydrate is InChI=1S/C2H6O6S2.2H2O/c3-9(4,5)1-2-10(6,7)8;;/h1-2H2,(H,3,4,5)(H,6,7,8);2*1H2.
The InChIKey of 1,2-Ethanedisulfonic acid dihydrate is DSGUSEBCDAKBCM-UHFFFAOYSA-N.
The canonical SMILES of 1,2-Ethanedisulfonic acid dihydrate is C(CS(=O)(=O)O)S(=O)(=O)O.O.O.
The CAS number of 1,2-Ethanedisulfonic acid dihydrate is 5982-56-9.
Some computed properties of 1,2-Ethanedisulfonic acid dihydrate include a hydrogen bond donor count of 4, a hydrogen bond acceptor count of 8, a rotatable bond count of 3, an exact mass of 225.98170962 g/mol, and a topological polar surface area of 128Ų.
Reference: [1]Patent: US2004/116422,2004,A1 .Location in patent: Page/Page column 45
* For details of the synthesis route, please refer to the original source to ensure accuracy.