Twofold Interpenetrated Cationic Metal–Organic Framework with Hydrophobic Channels for Effectively Trapping Toxic Oxo-Anions

Abstract

Sequestration of toxic oxo-anions (such as 99 TcO 4 − and ClO 4 − ) from wastewater has received constant attention due to the existing serious threat to public health and the sustainability of the environment. In view of the low energy of hydration of TcO 4 − and ClO 4 − , cationic metal−organic framework (MOF) materials with the hydrophobic microenvironment are preferred in the selection of sorbents. Herein, a twofold interpenetrated cationic MOF (ZJU-X15) with double-helical chains was constructed by tetrakis[4-(pyridin-4-yl)phenyl]ethene (TPPE) and Cd 2+ for the elimination of 99 TcO 4 − and ClO 4 − . Profiting from hydrophobic channels, ZJU-X15 could remove most of ReO 4 − (a surrogate for 99 TcO 4 − ) and ClO 4 − in less than 10 and 20 min, respectively. As the result of batch experiments, ZJU-X15 could capture 356 mg of ReO 4− and 221 mg of ClO 4 − per 1 g of sorbent, showcase decent selectivity, and still maintain high removal efficiency for anions after four recycles. Furthermore, the process of anion-exchange was confirmed by ion chromatography, Fourier-transform infrared spectroscopy, scanning electron microscopy combined with an energy-dispersive X-ray spectrometer, and X-ray photoelectron spectroscopy, indicating that target anions successfully entered into the body of ZJU-X15 through anion exchange.

Metal–organic framework-based adsorbents for blood purification: progress, challenges, and prospects

“…3(e)). 79,80 Recently, Zhang et al designed two cationic MOFs: ZJU-X6(Ni) and ZJU-X7(Ag) (Fig. 3(f)).…”

Controlling aggregation-induced emission by supramolecular interactions and colloidal stability in ionic emitters for light-emitting electrochemical cells

“…Herein we present a new versatile platform of positively charged structures derived from tetra-(4-pyridylphenyl)ethylene 1,1,2,2-tetrakis(4-(pyridin-4-yl)phenyl)ethene (TPPE) that exhibits AIE effect upon aggregation. [24][25][26][27][28] They present a propeller-like structure formed by four phenyl groups moving freely in the monomeric state. The hydrophilic/ hydrophobic balance governing the AIE effect is nely tuned by the length of alkyl chain and the counterion: on one hand, the hydrophilicity is introduced by the positively charged pyridinium moieties that increase the solubility in aqueous media.…”

Controlling Aggregation-Induced Emission by Supramolecular Interactions and Colloidal Stability in Ionic Emitters for Light-Emitting Electrochemical Cells

“…Herein we present a new versatile platform of positively charged structures derived from tetra-(4pyridylphenyl)-ethylene 1,1,2,2-tetrakis(4-(pyridin-4-yl)phenyl)ethene (TPPE) that exhibits AIE effect upon aggregation. [24][25][26][27][28] They present a propeller-like structure formed by four phenyl groups moving freely in the monomeric state. The hydrophilic/hydrophobic balance governing the AIE effect is finely tuned by the length of alkyl chain and the counterion: on one hand, the hydrophilicity is introduced by the positively charged pyridinium moieties that increase the solubility in aqueous media.…”