Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction
In the present study, heterogenization of amine-functionalized ionic liquids was developed via covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infra...
Gespeichert in:
Veröffentlicht in: | New journal of chemistry 2017, Vol.41 (24), p.15545-15554 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15554 |
---|---|
container_issue | 24 |
container_start_page | 15545 |
container_title | New journal of chemistry |
container_volume | 41 |
creator | Garkoti, Charu Shabir, Javaid Gupta, Padmini Sharma, Manisha Mozumdar, Subho |
description | In the present study, heterogenization of amine-functionalized ionic liquids was developed
via
covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The prepared material was employed as an efficient heterogeneous catalyst for the synthesis of 3-substituted indoles
via
Yonemitsu-type reaction. The catalyst could be easily separated from the reaction mixture through centrifugation and could be reused for seven consecutive cycles without any appreciable loss in its catalytic activity. |
doi_str_mv | 10.1039/C7NJ03450D |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2010876590</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2010876590</sourcerecordid><originalsourceid>FETCH-LOGICAL-c259t-f40f16df1252a6ed69e59b086d7b86cb87d028c425b8481001a092c72342ad633</originalsourceid><addsrcrecordid>eNpFUU1v1TAQjBBIlJYLv2AlbkgB20mchBt6fBRUlUs5cIqceP3eVnl26rUR6f_r_yKPInGa0Wg0s5otildSvJWi6t_t2utvoqob8fFJcSYr3Ze90vLpxmVdl6Kp9fPiBfOtEFK2Wp4VD5eYMIY9ero3iYKH4MAcyWPpsp9OipnpHi1sjCaY6S6TZchMfg_7aJYDeoTwmyyCYTDAeVlCTHA0WzCZ-f2mHWh_mFdA52gi9Akmk8y8cgIXIqQDAq9-AyY-9Vcl55ETpZxOxd6GGRl-kYGfweOREucyrQtCRPP3xIvimTMz48t_eF78-PzpZndZXn3_8nX34aqcVNOn0tXCSW2dVI0yGq3uselH0Wnbjp2exq61QnVTrZqxqzu5jWREr6ZWVbUyVlfVefH6MXeJ4S4jp-E25LgtxIMSUnStbnqxud48uqYYmCO6YYl0NHEdpBhObxr-v6n6A-3Dico</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2010876590</pqid></control><display><type>article</type><title>Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Garkoti, Charu ; Shabir, Javaid ; Gupta, Padmini ; Sharma, Manisha ; Mozumdar, Subho</creator><creatorcontrib>Garkoti, Charu ; Shabir, Javaid ; Gupta, Padmini ; Sharma, Manisha ; Mozumdar, Subho</creatorcontrib><description>In the present study, heterogenization of amine-functionalized ionic liquids was developed
via
covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The prepared material was employed as an efficient heterogeneous catalyst for the synthesis of 3-substituted indoles
via
Yonemitsu-type reaction. The catalyst could be easily separated from the reaction mixture through centrifugation and could be reused for seven consecutive cycles without any appreciable loss in its catalytic activity.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/C7NJ03450D</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Catalysis ; Catalysts ; Catalytic activity ; Chemical synthesis ; Electron microscopy ; Energy dispersive X ray spectroscopy ; Energy transmission ; Fourier transforms ; Graphene ; Imidazole ; Indoles ; Infrared analysis ; Infrared spectroscopy ; Ionic liquids ; Scanning electron microscopy ; Spectrum analysis ; Substitutes ; Thermogravimetric analysis ; X ray powder diffraction ; X-ray diffraction ; X-rays</subject><ispartof>New journal of chemistry, 2017, Vol.41 (24), p.15545-15554</ispartof><rights>Copyright Royal Society of Chemistry 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c259t-f40f16df1252a6ed69e59b086d7b86cb87d028c425b8481001a092c72342ad633</citedby><cites>FETCH-LOGICAL-c259t-f40f16df1252a6ed69e59b086d7b86cb87d028c425b8481001a092c72342ad633</cites><orcidid>0000-0002-6526-8839</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4023,27922,27923,27924</link.rule.ids></links><search><creatorcontrib>Garkoti, Charu</creatorcontrib><creatorcontrib>Shabir, Javaid</creatorcontrib><creatorcontrib>Gupta, Padmini</creatorcontrib><creatorcontrib>Sharma, Manisha</creatorcontrib><creatorcontrib>Mozumdar, Subho</creatorcontrib><title>Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction</title><title>New journal of chemistry</title><description>In the present study, heterogenization of amine-functionalized ionic liquids was developed
via
covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The prepared material was employed as an efficient heterogeneous catalyst for the synthesis of 3-substituted indoles
via
Yonemitsu-type reaction. The catalyst could be easily separated from the reaction mixture through centrifugation and could be reused for seven consecutive cycles without any appreciable loss in its catalytic activity.</description><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemical synthesis</subject><subject>Electron microscopy</subject><subject>Energy dispersive X ray spectroscopy</subject><subject>Energy transmission</subject><subject>Fourier transforms</subject><subject>Graphene</subject><subject>Imidazole</subject><subject>Indoles</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>Ionic liquids</subject><subject>Scanning electron microscopy</subject><subject>Spectrum analysis</subject><subject>Substitutes</subject><subject>Thermogravimetric analysis</subject><subject>X ray powder diffraction</subject><subject>X-ray diffraction</subject><subject>X-rays</subject><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpFUU1v1TAQjBBIlJYLv2AlbkgB20mchBt6fBRUlUs5cIqceP3eVnl26rUR6f_r_yKPInGa0Wg0s5otildSvJWi6t_t2utvoqob8fFJcSYr3Ze90vLpxmVdl6Kp9fPiBfOtEFK2Wp4VD5eYMIY9ero3iYKH4MAcyWPpsp9OipnpHi1sjCaY6S6TZchMfg_7aJYDeoTwmyyCYTDAeVlCTHA0WzCZ-f2mHWh_mFdA52gi9Akmk8y8cgIXIqQDAq9-AyY-9Vcl55ETpZxOxd6GGRl-kYGfweOREucyrQtCRPP3xIvimTMz48t_eF78-PzpZndZXn3_8nX34aqcVNOn0tXCSW2dVI0yGq3uselH0Wnbjp2exq61QnVTrZqxqzu5jWREr6ZWVbUyVlfVefH6MXeJ4S4jp-E25LgtxIMSUnStbnqxud48uqYYmCO6YYl0NHEdpBhObxr-v6n6A-3Dico</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Garkoti, Charu</creator><creator>Shabir, Javaid</creator><creator>Gupta, Padmini</creator><creator>Sharma, Manisha</creator><creator>Mozumdar, Subho</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H9R</scope><scope>JG9</scope><scope>KA0</scope><orcidid>https://orcid.org/0000-0002-6526-8839</orcidid></search><sort><creationdate>2017</creationdate><title>Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction</title><author>Garkoti, Charu ; Shabir, Javaid ; Gupta, Padmini ; Sharma, Manisha ; Mozumdar, Subho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c259t-f40f16df1252a6ed69e59b086d7b86cb87d028c425b8481001a092c72342ad633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Catalysis</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Chemical synthesis</topic><topic>Electron microscopy</topic><topic>Energy dispersive X ray spectroscopy</topic><topic>Energy transmission</topic><topic>Fourier transforms</topic><topic>Graphene</topic><topic>Imidazole</topic><topic>Indoles</topic><topic>Infrared analysis</topic><topic>Infrared spectroscopy</topic><topic>Ionic liquids</topic><topic>Scanning electron microscopy</topic><topic>Spectrum analysis</topic><topic>Substitutes</topic><topic>Thermogravimetric analysis</topic><topic>X ray powder diffraction</topic><topic>X-ray diffraction</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garkoti, Charu</creatorcontrib><creatorcontrib>Shabir, Javaid</creatorcontrib><creatorcontrib>Gupta, Padmini</creatorcontrib><creatorcontrib>Sharma, Manisha</creatorcontrib><creatorcontrib>Mozumdar, Subho</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Illustrata: Natural Sciences</collection><collection>Materials Research Database</collection><collection>ProQuest Illustrata: Technology Collection</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garkoti, Charu</au><au>Shabir, Javaid</au><au>Gupta, Padmini</au><au>Sharma, Manisha</au><au>Mozumdar, Subho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction</atitle><jtitle>New journal of chemistry</jtitle><date>2017</date><risdate>2017</risdate><volume>41</volume><issue>24</issue><spage>15545</spage><epage>15554</epage><pages>15545-15554</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>In the present study, heterogenization of amine-functionalized ionic liquids was developed
via
covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The prepared material was employed as an efficient heterogeneous catalyst for the synthesis of 3-substituted indoles
via
Yonemitsu-type reaction. The catalyst could be easily separated from the reaction mixture through centrifugation and could be reused for seven consecutive cycles without any appreciable loss in its catalytic activity.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/C7NJ03450D</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6526-8839</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1144-0546 |
ispartof | New journal of chemistry, 2017, Vol.41 (24), p.15545-15554 |
issn | 1144-0546 1369-9261 |
language | eng |
recordid | cdi_proquest_journals_2010876590 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Catalysis Catalysts Catalytic activity Chemical synthesis Electron microscopy Energy dispersive X ray spectroscopy Energy transmission Fourier transforms Graphene Imidazole Indoles Infrared analysis Infrared spectroscopy Ionic liquids Scanning electron microscopy Spectrum analysis Substitutes Thermogravimetric analysis X ray powder diffraction X-ray diffraction X-rays |
title | Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T03%3A48%3A36IST&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=Heterogenization%20of%20amine-functionalized%20ionic%20liquids%20using%20graphene%20oxide%20as%20a%20support%20material:%20a%20highly%20efficient%20catalyst%20for%20the%20synthesis%20of%203-substituted%20indoles%20via%20Yonemitsu-type%20reaction&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Garkoti,%20Charu&rft.date=2017&rft.volume=41&rft.issue=24&rft.spage=15545&rft.epage=15554&rft.pages=15545-15554&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/C7NJ03450D&rft_dat=%3Cproquest_cross%3E2010876590%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=2010876590&rft_id=info:pmid/&rfr_iscdi=true |