2017
DOI: 10.1021/acs.inorgchem.7b01835
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Postsynthesis Modification of a Metallosalen-Containing Metal–Organic Framework for Selective Th(IV)/Ln(III) Separation

Abstract: An uncoordinated salen-containing metal-organic framework (MOF) obtained through postsynthesis removal of Mn(III) ions from a metallosalen-containing MOF material has been used for selective separation of Th(IV) ion from Ln(III) ions in methanol solutions for the first time. This material exhibited an adsorption capacity of 46.345 mg of Th/g. The separation factors (β) of Th(IV)/La(III), Th(IV)/Eu(III), and Th(IV)/Lu(III) were 10.7, 16.4, and 10.3, respectively.

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Cited by 55 publications
(18 citation statements)
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References 38 publications
(46 reference statements)
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“…According to Guo et al, [ 35 ] 3‐ tert ‐ butyl ‐salicylaldehyde (178.23 mg, 1.0 mmol) was dissolved in two‐neck round bottom flask containing 20 ml of dichloromethane and 1.5 ml of liquid bromine, was drawn with a syringe, and injected into a constant pressure drop funnel containing 15 ml of dichloromethane. Keep the system sealed to a temperature of 0°C.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…According to Guo et al, [ 35 ] 3‐ tert ‐ butyl ‐salicylaldehyde (178.23 mg, 1.0 mmol) was dissolved in two‐neck round bottom flask containing 20 ml of dichloromethane and 1.5 ml of liquid bromine, was drawn with a syringe, and injected into a constant pressure drop funnel containing 15 ml of dichloromethane. Keep the system sealed to a temperature of 0°C.…”
Section: Methodsmentioning
confidence: 99%
“…According to Guo et al, [35] 3-tert-butyl-salicylaldehyde (178.23 mg, 1.0 mmol) was dissolved in two-neck round bottom flask containing 20 ml of dichloromethane and 1.5 ml of liquid bromine, was drawn with a syringe, and injected into a constant pressure drop funnel containing 15 ml of dichloromethane. Keep the system sealed to a temperature of 0 C. Slowly add the brominated dichloromethane solution to the round bottom flask, and keep the temperature constant and react 1.5 h. After, anhydrous sodium sulfite solution (20 ml) was poured into the reactor and continued 0.5 h. Stop the reaction, the liquid was separated with a separating funnel, leaving the organic phase.…”
Section: The Synthesis Of 3-tert-butyl-5-bromosalicylaldehydementioning
confidence: 99%
“…(III) [229][230][231][232][233][234][235][236], Cr(II) [234], Co(II) [234], Mn(II) [234], Ni(II) [234], Cu(II) [234][235][236][237][238], Zn(II) [234], V(IV) [235], Cr(III) [235], Fe(III) [235], Co(III) [235], Th(IV) [236]…”
Section: Zn (Ii) Mnmentioning
confidence: 99%
“…A specific framework can be produced by designing the combination of metal nodes and organic ligands due to the fixed coordination geometries. The structure and properties can be tuned by presynthesis [12][13][14][15][16][17] or postsynthesis [18][19][20][21][22][23] design of ligands and secondary building unit (SBU). More recently, many studies have shown that the properties of MOFs could also be modified by introducing guest components into their cavities [24][25][26][27][28][29][30].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, MOFs demonstrate great potential applications in various fields. Owing to the decades' efforts of researchers, thousands of structures of MOFs have been discovered and applied in various fields, such as separation [31][32][33][34][35][36][37][38], adsorption [20,[39][40][41][42], optics [43][44][45][46][47][48][49][50], catalysis [19,[51][52][53][54][55][56], sensors [57][58][59][60][61][62][63], etc. However, most of these studies are based on MOFs powders.…”
Section: Introductionmentioning
confidence: 99%