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Complexation of uranyl ions by N-(sulfoethyl)-iminodiacetic acid:hydrothermal synthesis, luminescence, and uranyl sequestration

Complexation of uranyl ions by N-(sulfoethyl)-iminodiacetic acid:hydrothermal synthesis, luminescence, and uranyl sequestration
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摘要 Reported here is a water-soluble ligand, N-(sulfoethyl)-iminodiacetic acid (H3SEIDA), used for the complexation of uranyl ions. A coordination compound composed of uranyl cation and N-(sulfonatoethyl)-ammoniodiacetate (SEADA2-) zwitterion was synthesized from an acidic aqueous solution. This compound features a 2D undulating fes (4.82) coordination layer that is stacked and linked by hydrogen-bonding interaction to form a 3D supramolecular framework with a 1D larger-cycle channel. Thermal analysis demonstrates the relatively weak bonding between uranyl cation and SEADA2 zwitterion. The monomeric uranyl-based fluorescence emission is red-shifted by about thermal synthesis of this uranyl compound was successfully 5 nm compared to that of uranyl nitrate hexahydrate. The hydro- applied to the sequestration of uranyl ions. Reported here is a water-soluble ligand, N-(sulfoethyl)-iminodiacetic acid(H3SEIDA), used for the complexation of uranyl ions. A coordination compound composed of uranyl cation and N-(sulfonatoethyl)-ammoniodiacetate(SEADA2?) zwitterion was synthesized from an acidic aqueous solution. This compound features a 2D undulating fes(4.82) coordination layer that is stacked and linked by hydrogen-bonding interaction to form a 3D supramolecular framework with a 1D larger-cycle channel. Thermal analysis demonstrates the relatively weak bonding between uranyl cation and SEADA2? zwitterion. The monomeric uranyl-based fluorescence emission is red-shifted by about 5 nm compared to that of uranyl nitrate hexahydrate. The hydrothermal synthesis of this uranyl compound was successfully applied to the sequestration of uranyl ions.
出处 《Science China Chemistry》 SCIE EI CAS CSCD 2015年第5期845-849,共5页 中国科学(化学英文版)
基金 financially supported by the National Natural Science Foundation of China(91122007) the Specialized Research Fund for the Doctoral Program of Higher Education(20110211130002)
关键词 uranium water-soluble ligand hydrothermal synthesis LUMINESCENCE selective precipitation 亚氨基二乙酸 铀酰离子 水热合成 络合 配位化合物 发光 磺基 封存
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  • 1Wang KX, Chen JS. Extended structures and physicochemical prop- erties of uranyl-organic compounds. Acc Chem Res, 2011, 44: 531- 540.
  • 2Andrews MB, Cahill CL. Uranyl bearing hybrid materials: synthesis, speciation, and solid-state structures. Chern Rev, 2013, 113: 1121- 1136.
  • 3Nash KL, Horwitz EP, Diamond H, Rickert PG, Muntean JV, Men- doza MD, Di Giuseppe G. Selective separation of uranyl ion from tru's in a combined solvent extraction process using tetrahydrofuran- 2,3,4,5-tetracarboxylic acid. Solvent ExtrIon Exch, 1996, 14:13-33.
  • 4Morss LR, Nash KL, Ensor DD. Thermodynamics of lanthanide and uranyl complexes with tetrahydrofuran-2,3,4,5-tetracarboxylic acid (THFTCA). J Chem Soc, Dalton Trans, 2000:285-291.
  • 5Sather AC, Berryman OB, Rebek Jr J. Selective recognition and ex- traction of the uranyl ion. JAm Chem Soc, 2010, 132:13572-13574.
  • 6Riisii3 A, Vaiisainen A, Sillanpaa R. Uranyl complexes of alkyl- bridged ditopic diaminotetraphenol ligands and their use as uranyl ion extractors. Inorg Chem, 2013, 52:8591-8600.
  • 7Tokunaga TK, Kim Y, Wan J. Potential remediation approach for uranium-contaminated groundwaters through potassium uranyl van- adate precipitation. Environ Sci Technol, 2009, 43:5467-5471.
  • 8Tokunaga TK, Kim Y, Wan J, Yang L. Aqueous uranium(Ⅵ) con- centrations controlled by calcium uranyl vanadate precipitates. Environ Sci Technol, 2012, 46:7471-7477.
  • 9Rao L, Gamov AY, Jiang 1, Di Bernardo P, Zanonato P, Bismondo A Complexation of uranium(Ⅵ) and samarium(Ⅲ) with oxydiacetic acid: temperature effect and coordination modes. Inorg Chem, 2003, 42:3685-3692.
  • 10Di Bernardo P, Zanonato P, Bismondo A, Jiang H, Garnov AY, Jiang J, Rao L. Complexation of uranium(Ⅵ) with thiodiacetic acid in so- lution at 10-85 ℃. Eur J lnorg Chem, 2006:4533-4540.

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