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Redox‐Responsive Covalent Organic Nanosheets from Viologens and Calix[4]arene for Iodine and Toxic Dye Capture

Owing to their chemical and thermal stabilities, high uptake capacities, and easy recyclability, covalent organic polymers (COPs) have shown promise as pollutant sponges. Herein, we describe the use of diazo coupling to synthesize two cationic COPs, COP1++ and COP2++, that incorporate a viologen‐bas...

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Published in:Chemistry : a European journal 2018-06, Vol.24 (34), p.8648-8655
Main Authors: Skorjanc, Tina, Shetty, Dinesh, Sharma, Sudhir Kumar, Raya, Jesus, Traboulsi, Hassan, Han, Dong Suk, Lalla, Jayesh, Newlon, Ryan, Jagannathan, Ramesh, Kirmizialtin, Serdal, Olsen, John‐Carl, Trabolsi, Ali
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creator Skorjanc, Tina
Shetty, Dinesh
Sharma, Sudhir Kumar
Raya, Jesus
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Jagannathan, Ramesh
Kirmizialtin, Serdal
Olsen, John‐Carl
Trabolsi, Ali
description Owing to their chemical and thermal stabilities, high uptake capacities, and easy recyclability, covalent organic polymers (COPs) have shown promise as pollutant sponges. Herein, we describe the use of diazo coupling to synthesize two cationic COPs, COP1++ and COP2++, that incorporate a viologen‐based molecular switch and an organic macrocycle, calix[4]arene. The COPs form nanosheets that have height profiles of 6.00 nm and 8.00 nm, respectively, based on AFM measurements. The sheets remain morphologically intact upon one‐ or two‐electron reductions of their viologen subunits. MD simulations of the COPs containing dicationic viologens indicate that the calix[4]arenes adopt a partial cone conformation and that, in height, the individual 2D polymer layers are 5.48 Å in COP1++ and 5.65 Å in COP2++, which, together with the AFM measurements, suggests that the nanosheets are composed of 11 and 14 layers, respectively. Whether their viologens are in dicationic, radical cationic, or neutral form, the COPs exhibit high affinity for iodine, reaching up to 200 % mass increase when exposed to iodine vapor at 70 °C, which makes the materials among the best‐performing nanosheets for iodine capture reported in the literature. In addition, the COPs effectively remove Congo red from solution in the pH range of 2–10, reaching nearly 100 % removal within 15 minutes at acidic pH. Two cationic covalent organic polymers (COPs) were synthesized by diazo coupling of a calix[4]arene derivative and viologen‐based, redox‐responsive linkers. Interestingly, the COPs exhibit nanosheet morphology consistent with MD simulations. Because of their cationic and aromatic nature, these materials serve as efficient sponges for iodine and for organic dyes over a broad pH range (see figure).
doi_str_mv 10.1002/chem.201800623
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Whether their viologens are in dicationic, radical cationic, or neutral form, the COPs exhibit high affinity for iodine, reaching up to 200 % mass increase when exposed to iodine vapor at 70 °C, which makes the materials among the best‐performing nanosheets for iodine capture reported in the literature. In addition, the COPs effectively remove Congo red from solution in the pH range of 2–10, reaching nearly 100 % removal within 15 minutes at acidic pH. Two cationic covalent organic polymers (COPs) were synthesized by diazo coupling of a calix[4]arene derivative and viologen‐based, redox‐responsive linkers. Interestingly, the COPs exhibit nanosheet morphology consistent with MD simulations. 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source Wiley-Blackwell Read & Publish Collection
subjects Aromatic compounds
calixarenes
Cations
Chemistry
Conformation
Congo red
Coupling (molecular)
Iodine
iodine capture
Molecular chains
Molecular machines
Nanosheets
Organic chemistry
pH effects
Pollutants
Polymers
Recyclability
viologen
title Redox‐Responsive Covalent Organic Nanosheets from Viologens and Calix[4]arene for Iodine and Toxic Dye Capture
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