Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks

Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross‐linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic spe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemPlusChem (Weinheim, Germany) Germany), 2019-10, Vol.84 (10), p.1536-1543
Hauptverfasser: Calabrese, Carla, Fusaro, Luca, Liotta, Leonarda Francesca, Giacalone, Francesco, Comès, Adrien, Campisciano, Vincenzo, Aprile, Carmela, Gruttadauria, Michelangelo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1543
container_issue 10
container_start_page 1536
container_title ChemPlusChem (Weinheim, Germany)
container_volume 84
creator Calabrese, Carla
Fusaro, Luca
Liotta, Leonarda Francesca
Giacalone, Francesco
Comès, Adrien
Campisciano, Vincenzo
Aprile, Carmela
Gruttadauria, Michelangelo
description Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross‐linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid‐state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal‐ and solvent‐free reaction conditions showing full selectivity toward the formation of cyclic carbonates. High turnover number (TON) and productivity values, up to 5502 and 1081 respectively for glycidol conversion at 100 °C and up to 4942 and 1122 for epichlorohydrin conversion at 150 °C after 3 h, were obtained. Such outstanding productivity values were ascribed to the optimal organic/inorganic (i. e., imidazolium moiety/POSS support) weight ratio. The recyclability of the materials was successfully verified for five consecutive runs allowing their consideration as promising candidates for continuous flow technologies. Fast, simple and high‐yielding synthesis of polymeric cross‐linked imidazolium‐POSS materials for the efficient conversion of carbon dioxide and epoxides into cyclic carbonates has been achieved. Cyclic carbonates have been obtained with high TON and productivity values, up to 5502 and 1081 respectively for glycidol at 100 °C and up to 4942 and 1122 for epichlorohydrin at 150 °C.
doi_str_mv 10.1002/cplu.201900408
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2339795025</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2310231776</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3738-de85f14d923823b5e94a2c239d58d1a9bc7a0a64f9b74334b584ebba2e21b1163</originalsourceid><addsrcrecordid>eNqFkctuEzEUhi0EolXbLUtkiU1ZJPVlbl6SodBKEYkUuh75NsWtx07tMRBWPALP0EfjSfAopSA2WLJ8jvT585F_AF5gNMcIkTO5tWlOEGYIFah5Ag4JZmRWlah6-ld9AE5ivEF5VagkNX0ODihmBWWYHYL787430mg3wta7zzpE4x30PWx5ELl6a_xXozQUO3g5GMW_eWvS8PP7jwWPWsE2-BhztzTuNrcfuPNxDEmOKeg4GUdunHHXcO3t7pNWgVu4subaDzoYCTfGRh3vUn6EOw1P16vN5jVcJGPVdGlhvbyNx-BZzzN38nAegat35x_bi9ly9f6yfbOcSVrTZqZ0U_a4UIzQhlBRalZwIgllqmwU5kzImiNeFT0TdUFpIcqm0EJwogkWGFf0CJzuvdvg75KOYzeYKLW1eTSfYkcoZTUrESkz-uof9Man4PJ0mcIo77qehPM9JadfCrrvtsEMPOw6jLopwG4KsHsMMF94-aBNYtDqEf8dVwbYHvhirN79R9e16-XVH_kvWJqrcg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2310231776</pqid></control><display><type>article</type><title>Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Calabrese, Carla ; Fusaro, Luca ; Liotta, Leonarda Francesca ; Giacalone, Francesco ; Comès, Adrien ; Campisciano, Vincenzo ; Aprile, Carmela ; Gruttadauria, Michelangelo</creator><creatorcontrib>Calabrese, Carla ; Fusaro, Luca ; Liotta, Leonarda Francesca ; Giacalone, Francesco ; Comès, Adrien ; Campisciano, Vincenzo ; Aprile, Carmela ; Gruttadauria, Michelangelo</creatorcontrib><description>Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross‐linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid‐state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal‐ and solvent‐free reaction conditions showing full selectivity toward the formation of cyclic carbonates. High turnover number (TON) and productivity values, up to 5502 and 1081 respectively for glycidol conversion at 100 °C and up to 4942 and 1122 for epichlorohydrin conversion at 150 °C after 3 h, were obtained. Such outstanding productivity values were ascribed to the optimal organic/inorganic (i. e., imidazolium moiety/POSS support) weight ratio. The recyclability of the materials was successfully verified for five consecutive runs allowing their consideration as promising candidates for continuous flow technologies. Fast, simple and high‐yielding synthesis of polymeric cross‐linked imidazolium‐POSS materials for the efficient conversion of carbon dioxide and epoxides into cyclic carbonates has been achieved. Cyclic carbonates have been obtained with high TON and productivity values, up to 5502 and 1081 respectively for glycidol at 100 °C and up to 4942 and 1122 for epichlorohydrin at 150 °C.</description><identifier>ISSN: 2192-6506</identifier><identifier>EISSN: 2192-6506</identifier><identifier>DOI: 10.1002/cplu.201900408</identifier><identifier>PMID: 31943919</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Carbon dioxide ; carbon dioxide conversion ; Carbonates ; Catalysts ; Chemical analysis ; Chemical synthesis ; Chemistry ; Continuous flow ; Conversion ; cyclic carbonates ; Epichlorohydrin ; heterogeneous catalysis ; imidazolium salts ; Infrared analysis ; Infrared spectroscopy ; Iodides ; NMR spectroscopy ; Polyhedral oligomeric silsesquioxane ; polyhedral oligomeric silsesquioxanes ; Productivity ; Recyclability ; Selectivity ; Spectrum analysis ; Thermogravimetric analysis</subject><ispartof>ChemPlusChem (Weinheim, Germany), 2019-10, Vol.84 (10), p.1536-1543</ispartof><rights>2019 Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2019 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3738-de85f14d923823b5e94a2c239d58d1a9bc7a0a64f9b74334b584ebba2e21b1163</citedby><cites>FETCH-LOGICAL-c3738-de85f14d923823b5e94a2c239d58d1a9bc7a0a64f9b74334b584ebba2e21b1163</cites><orcidid>0000-0001-5301-8034 ; 0000-0001-5442-2469 ; 0000-0002-6990-8290 ; 0000-0001-7696-4568 ; 0000-0002-3193-3239 ; 0000-0001-8348-0764 ; 0000-0002-6952-0712</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcplu.201900408$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcplu.201900408$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31943919$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calabrese, Carla</creatorcontrib><creatorcontrib>Fusaro, Luca</creatorcontrib><creatorcontrib>Liotta, Leonarda Francesca</creatorcontrib><creatorcontrib>Giacalone, Francesco</creatorcontrib><creatorcontrib>Comès, Adrien</creatorcontrib><creatorcontrib>Campisciano, Vincenzo</creatorcontrib><creatorcontrib>Aprile, Carmela</creatorcontrib><creatorcontrib>Gruttadauria, Michelangelo</creatorcontrib><title>Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks</title><title>ChemPlusChem (Weinheim, Germany)</title><addtitle>Chempluschem</addtitle><description>Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross‐linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid‐state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal‐ and solvent‐free reaction conditions showing full selectivity toward the formation of cyclic carbonates. High turnover number (TON) and productivity values, up to 5502 and 1081 respectively for glycidol conversion at 100 °C and up to 4942 and 1122 for epichlorohydrin conversion at 150 °C after 3 h, were obtained. Such outstanding productivity values were ascribed to the optimal organic/inorganic (i. e., imidazolium moiety/POSS support) weight ratio. The recyclability of the materials was successfully verified for five consecutive runs allowing their consideration as promising candidates for continuous flow technologies. Fast, simple and high‐yielding synthesis of polymeric cross‐linked imidazolium‐POSS materials for the efficient conversion of carbon dioxide and epoxides into cyclic carbonates has been achieved. Cyclic carbonates have been obtained with high TON and productivity values, up to 5502 and 1081 respectively for glycidol at 100 °C and up to 4942 and 1122 for epichlorohydrin at 150 °C.</description><subject>Carbon dioxide</subject><subject>carbon dioxide conversion</subject><subject>Carbonates</subject><subject>Catalysts</subject><subject>Chemical analysis</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Continuous flow</subject><subject>Conversion</subject><subject>cyclic carbonates</subject><subject>Epichlorohydrin</subject><subject>heterogeneous catalysis</subject><subject>imidazolium salts</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>Iodides</subject><subject>NMR spectroscopy</subject><subject>Polyhedral oligomeric silsesquioxane</subject><subject>polyhedral oligomeric silsesquioxanes</subject><subject>Productivity</subject><subject>Recyclability</subject><subject>Selectivity</subject><subject>Spectrum analysis</subject><subject>Thermogravimetric analysis</subject><issn>2192-6506</issn><issn>2192-6506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkctuEzEUhi0EolXbLUtkiU1ZJPVlbl6SodBKEYkUuh75NsWtx07tMRBWPALP0EfjSfAopSA2WLJ8jvT585F_AF5gNMcIkTO5tWlOEGYIFah5Ag4JZmRWlah6-ld9AE5ivEF5VagkNX0ODihmBWWYHYL787430mg3wta7zzpE4x30PWx5ELl6a_xXozQUO3g5GMW_eWvS8PP7jwWPWsE2-BhztzTuNrcfuPNxDEmOKeg4GUdunHHXcO3t7pNWgVu4subaDzoYCTfGRh3vUn6EOw1P16vN5jVcJGPVdGlhvbyNx-BZzzN38nAegat35x_bi9ly9f6yfbOcSVrTZqZ0U_a4UIzQhlBRalZwIgllqmwU5kzImiNeFT0TdUFpIcqm0EJwogkWGFf0CJzuvdvg75KOYzeYKLW1eTSfYkcoZTUrESkz-uof9Man4PJ0mcIo77qehPM9JadfCrrvtsEMPOw6jLopwG4KsHsMMF94-aBNYtDqEf8dVwbYHvhirN79R9e16-XVH_kvWJqrcg</recordid><startdate>201910</startdate><enddate>201910</enddate><creator>Calabrese, Carla</creator><creator>Fusaro, Luca</creator><creator>Liotta, Leonarda Francesca</creator><creator>Giacalone, Francesco</creator><creator>Comès, Adrien</creator><creator>Campisciano, Vincenzo</creator><creator>Aprile, Carmela</creator><creator>Gruttadauria, Michelangelo</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5301-8034</orcidid><orcidid>https://orcid.org/0000-0001-5442-2469</orcidid><orcidid>https://orcid.org/0000-0002-6990-8290</orcidid><orcidid>https://orcid.org/0000-0001-7696-4568</orcidid><orcidid>https://orcid.org/0000-0002-3193-3239</orcidid><orcidid>https://orcid.org/0000-0001-8348-0764</orcidid><orcidid>https://orcid.org/0000-0002-6952-0712</orcidid></search><sort><creationdate>201910</creationdate><title>Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks</title><author>Calabrese, Carla ; Fusaro, Luca ; Liotta, Leonarda Francesca ; Giacalone, Francesco ; Comès, Adrien ; Campisciano, Vincenzo ; Aprile, Carmela ; Gruttadauria, Michelangelo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3738-de85f14d923823b5e94a2c239d58d1a9bc7a0a64f9b74334b584ebba2e21b1163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Carbon dioxide</topic><topic>carbon dioxide conversion</topic><topic>Carbonates</topic><topic>Catalysts</topic><topic>Chemical analysis</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Continuous flow</topic><topic>Conversion</topic><topic>cyclic carbonates</topic><topic>Epichlorohydrin</topic><topic>heterogeneous catalysis</topic><topic>imidazolium salts</topic><topic>Infrared analysis</topic><topic>Infrared spectroscopy</topic><topic>Iodides</topic><topic>NMR spectroscopy</topic><topic>Polyhedral oligomeric silsesquioxane</topic><topic>polyhedral oligomeric silsesquioxanes</topic><topic>Productivity</topic><topic>Recyclability</topic><topic>Selectivity</topic><topic>Spectrum analysis</topic><topic>Thermogravimetric analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calabrese, Carla</creatorcontrib><creatorcontrib>Fusaro, Luca</creatorcontrib><creatorcontrib>Liotta, Leonarda Francesca</creatorcontrib><creatorcontrib>Giacalone, Francesco</creatorcontrib><creatorcontrib>Comès, Adrien</creatorcontrib><creatorcontrib>Campisciano, Vincenzo</creatorcontrib><creatorcontrib>Aprile, Carmela</creatorcontrib><creatorcontrib>Gruttadauria, Michelangelo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>MEDLINE - Academic</collection><jtitle>ChemPlusChem (Weinheim, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calabrese, Carla</au><au>Fusaro, Luca</au><au>Liotta, Leonarda Francesca</au><au>Giacalone, Francesco</au><au>Comès, Adrien</au><au>Campisciano, Vincenzo</au><au>Aprile, Carmela</au><au>Gruttadauria, Michelangelo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks</atitle><jtitle>ChemPlusChem (Weinheim, Germany)</jtitle><addtitle>Chempluschem</addtitle><date>2019-10</date><risdate>2019</risdate><volume>84</volume><issue>10</issue><spage>1536</spage><epage>1543</epage><pages>1536-1543</pages><issn>2192-6506</issn><eissn>2192-6506</eissn><abstract>Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross‐linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid‐state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal‐ and solvent‐free reaction conditions showing full selectivity toward the formation of cyclic carbonates. High turnover number (TON) and productivity values, up to 5502 and 1081 respectively for glycidol conversion at 100 °C and up to 4942 and 1122 for epichlorohydrin conversion at 150 °C after 3 h, were obtained. Such outstanding productivity values were ascribed to the optimal organic/inorganic (i. e., imidazolium moiety/POSS support) weight ratio. The recyclability of the materials was successfully verified for five consecutive runs allowing their consideration as promising candidates for continuous flow technologies. Fast, simple and high‐yielding synthesis of polymeric cross‐linked imidazolium‐POSS materials for the efficient conversion of carbon dioxide and epoxides into cyclic carbonates has been achieved. Cyclic carbonates have been obtained with high TON and productivity values, up to 5502 and 1081 respectively for glycidol at 100 °C and up to 4942 and 1122 for epichlorohydrin at 150 °C.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>31943919</pmid><doi>10.1002/cplu.201900408</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5301-8034</orcidid><orcidid>https://orcid.org/0000-0001-5442-2469</orcidid><orcidid>https://orcid.org/0000-0002-6990-8290</orcidid><orcidid>https://orcid.org/0000-0001-7696-4568</orcidid><orcidid>https://orcid.org/0000-0002-3193-3239</orcidid><orcidid>https://orcid.org/0000-0001-8348-0764</orcidid><orcidid>https://orcid.org/0000-0002-6952-0712</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2192-6506
ispartof ChemPlusChem (Weinheim, Germany), 2019-10, Vol.84 (10), p.1536-1543
issn 2192-6506
2192-6506
language eng
recordid cdi_proquest_miscellaneous_2339795025
source Wiley Online Library Journals Frontfile Complete
subjects Carbon dioxide
carbon dioxide conversion
Carbonates
Catalysts
Chemical analysis
Chemical synthesis
Chemistry
Continuous flow
Conversion
cyclic carbonates
Epichlorohydrin
heterogeneous catalysis
imidazolium salts
Infrared analysis
Infrared spectroscopy
Iodides
NMR spectroscopy
Polyhedral oligomeric silsesquioxane
polyhedral oligomeric silsesquioxanes
Productivity
Recyclability
Selectivity
Spectrum analysis
Thermogravimetric analysis
title Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T19%3A09%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficient%20Conversion%20of%20Carbon%20Dioxide%20by%20Imidazolium%E2%80%90Based%20Cross%E2%80%90Linked%20Nanostructures%20Containing%20Polyhedral%20Oligomeric%20Silsesquioxane%20(POSS)%20Building%20Blocks&rft.jtitle=ChemPlusChem%20(Weinheim,%20Germany)&rft.au=Calabrese,%20Carla&rft.date=2019-10&rft.volume=84&rft.issue=10&rft.spage=1536&rft.epage=1543&rft.pages=1536-1543&rft.issn=2192-6506&rft.eissn=2192-6506&rft_id=info:doi/10.1002/cplu.201900408&rft_dat=%3Cproquest_cross%3E2310231776%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2310231776&rft_id=info:pmid/31943919&rfr_iscdi=true