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High Ethene/Ethane Selectivity in 2,2′‐Bipyridine‐Based Silver(I) Complexes by Removal of Coordinated Solvent
Authors:Dr. Matthew G. Cowan  William M. McDanel  Prof. Hans H. Funke  Dr. Yuki Kohno  Prof. Douglas L. Gin  Prof. Richard D. Noble
Affiliation:1. Dept. of Chemical & Biological Engineering, University of Colorado, Boulder, CO, 80309‐0424 (USA);2. Dept. of Chemistry & Biochemistry, University of Colorado, Boulder, CO, 80309‐0215 (USA)
Abstract:Following removal of coordinated CH3CN, the resulting complexes [AgI(2,2′‐bipyridine)][BF4] ( 1 ) and [AgI(6,6′‐dimethyl‐2,2′‐bipyridine)][OTf] ( 2 ) show ethene/ethane sorption selectivities of 390 and 340, respectively, and corresponding ethene sorption capacities of 2.38 and 2.18 mmol g?1 when tested at an applied gas pressure of 90 kPa and a temperature of (20±1) °C. These ethene/ethane selectivities are 13 times higher than those reported for known solid sorbents for ethene/ethane separation. For 2 , ethene sorption reached 90 % of equilibrium capacity within 15 minutes, and this equilibrium capacity was maintained over the three sorption/desorption cycles tested. The rates of ethene sorption were also measured. To our knowledge, these are the first complexes, designed for olefin/paraffin separations, which have open silver(I) sites. The high selectivities arise from these open silver(I) sites and the relatively low molecular surface areas of the complexes.
Keywords:adsorption  alkenes  coordination modes  silver  solvent effects
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