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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 |
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creator | 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 |
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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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).</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201800623</identifier><identifier>PMID: 29665187</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Chemistry : a European journal, 2018-06, Vol.24 (34), p.8648-8655</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4103-aff1c730d2b99891308475cef1d57691f9326b4184170a625567a455d8bbb3103</citedby><cites>FETCH-LOGICAL-c4103-aff1c730d2b99891308475cef1d57691f9326b4184170a625567a455d8bbb3103</cites><orcidid>0000-0001-7494-7887</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29665187$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skorjanc, Tina</creatorcontrib><creatorcontrib>Shetty, Dinesh</creatorcontrib><creatorcontrib>Sharma, Sudhir Kumar</creatorcontrib><creatorcontrib>Raya, Jesus</creatorcontrib><creatorcontrib>Traboulsi, Hassan</creatorcontrib><creatorcontrib>Han, Dong Suk</creatorcontrib><creatorcontrib>Lalla, Jayesh</creatorcontrib><creatorcontrib>Newlon, Ryan</creatorcontrib><creatorcontrib>Jagannathan, Ramesh</creatorcontrib><creatorcontrib>Kirmizialtin, Serdal</creatorcontrib><creatorcontrib>Olsen, John‐Carl</creatorcontrib><creatorcontrib>Trabolsi, Ali</creatorcontrib><title>Redox‐Responsive Covalent Organic Nanosheets from Viologens and Calix[4]arene for Iodine and Toxic Dye Capture</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><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).</description><subject>Aromatic compounds</subject><subject>calixarenes</subject><subject>Cations</subject><subject>Chemistry</subject><subject>Conformation</subject><subject>Congo red</subject><subject>Coupling (molecular)</subject><subject>Iodine</subject><subject>iodine capture</subject><subject>Molecular chains</subject><subject>Molecular machines</subject><subject>Nanosheets</subject><subject>Organic chemistry</subject><subject>pH effects</subject><subject>Pollutants</subject><subject>Polymers</subject><subject>Recyclability</subject><subject>viologen</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKxDAUQIMoOj62LiXgumNu0iTNUur4AB8g6kakpO2tVjpNTWZ0Zucn-I1-iR3Gx9JVLuTcc-EQsgtsCIzxg-IJx0POIGFMcbFCBiA5REIruUoGzMQ6UlKYDbIZwjNjzCgh1skGN0pJSPSAdNdYutnn-8c1hs61oX5FmrpX22A7oVf-0bZ1QS9t68IT4iTQyrsxvatd4x6xDdS2JU1tU8_u4wfrsUVaOU_PXFn34-Lzxs16wdG8t9puMvW4TdYq2wTc-X63yO3x6CY9jc6vTs7Sw_OoiIGJyFYVFFqwkufGJAYES2ItC6yglFoZqIzgKo8hiUEzq7iUSttYyjLJ81z0hi2yv_R23r1MMUyyZzf1bX8y40xq0AAcemq4pArvQvBYZZ2vx9bPM2DZInC2CJz9Bu4X9r6103yM5S_-U7QHzBJ4qxuc_6PL0tPRxZ_8CzkIh4o</recordid><startdate>20180618</startdate><enddate>20180618</enddate><creator>Skorjanc, Tina</creator><creator>Shetty, Dinesh</creator><creator>Sharma, Sudhir Kumar</creator><creator>Raya, Jesus</creator><creator>Traboulsi, Hassan</creator><creator>Han, Dong Suk</creator><creator>Lalla, Jayesh</creator><creator>Newlon, Ryan</creator><creator>Jagannathan, Ramesh</creator><creator>Kirmizialtin, Serdal</creator><creator>Olsen, John‐Carl</creator><creator>Trabolsi, Ali</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0001-7494-7887</orcidid></search><sort><creationdate>20180618</creationdate><title>Redox‐Responsive Covalent Organic Nanosheets from Viologens and Calix[4]arene for Iodine and Toxic Dye Capture</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4103-aff1c730d2b99891308475cef1d57691f9326b4184170a625567a455d8bbb3103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aromatic compounds</topic><topic>calixarenes</topic><topic>Cations</topic><topic>Chemistry</topic><topic>Conformation</topic><topic>Congo red</topic><topic>Coupling (molecular)</topic><topic>Iodine</topic><topic>iodine capture</topic><topic>Molecular chains</topic><topic>Molecular machines</topic><topic>Nanosheets</topic><topic>Organic chemistry</topic><topic>pH effects</topic><topic>Pollutants</topic><topic>Polymers</topic><topic>Recyclability</topic><topic>viologen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skorjanc, Tina</creatorcontrib><creatorcontrib>Shetty, Dinesh</creatorcontrib><creatorcontrib>Sharma, Sudhir Kumar</creatorcontrib><creatorcontrib>Raya, Jesus</creatorcontrib><creatorcontrib>Traboulsi, Hassan</creatorcontrib><creatorcontrib>Han, Dong Suk</creatorcontrib><creatorcontrib>Lalla, Jayesh</creatorcontrib><creatorcontrib>Newlon, Ryan</creatorcontrib><creatorcontrib>Jagannathan, Ramesh</creatorcontrib><creatorcontrib>Kirmizialtin, Serdal</creatorcontrib><creatorcontrib>Olsen, John‐Carl</creatorcontrib><creatorcontrib>Trabolsi, Ali</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skorjanc, Tina</au><au>Shetty, Dinesh</au><au>Sharma, Sudhir Kumar</au><au>Raya, Jesus</au><au>Traboulsi, Hassan</au><au>Han, Dong Suk</au><au>Lalla, Jayesh</au><au>Newlon, Ryan</au><au>Jagannathan, Ramesh</au><au>Kirmizialtin, Serdal</au><au>Olsen, John‐Carl</au><au>Trabolsi, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Redox‐Responsive Covalent Organic Nanosheets from Viologens and Calix[4]arene for Iodine and Toxic Dye Capture</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2018-06-18</date><risdate>2018</risdate><volume>24</volume><issue>34</issue><spage>8648</spage><epage>8655</epage><pages>8648-8655</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>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).</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29665187</pmid><doi>10.1002/chem.201800623</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7494-7887</orcidid></addata></record> |
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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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