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Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous
SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellen...
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Published in: | Catalysts 2024-09, Vol.14 (9), p.629 |
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description | SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity. |
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The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity.</description><identifier>ISSN: 2073-4344</identifier><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal14090629</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adsorption ; Alkylation ; Carbon ; Catalysts ; Catalytic activity ; Chemical synthesis ; Diketones ; Fine chemicals ; Green technology ; heterogeneous catalyst ; ionic liquid ; Ionic liquids ; mesoporous silica ; Morphology ; N-alkylated indoline-2,3-dione ; NMR ; Nuclear magnetic resonance ; Pore size ; SBA-15 ; Scanning electron microscopy ; Solid state ; Thermal stability ; Thermogravimetric analysis</subject><ispartof>Catalysts, 2024-09, Vol.14 (9), p.629</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity.</description><subject>Adsorption</subject><subject>Alkylation</subject><subject>Carbon</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemical synthesis</subject><subject>Diketones</subject><subject>Fine chemicals</subject><subject>Green technology</subject><subject>heterogeneous catalyst</subject><subject>ionic liquid</subject><subject>Ionic liquids</subject><subject>mesoporous silica</subject><subject>Morphology</subject><subject>N-alkylated indoline-2,3-dione</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pore size</subject><subject>SBA-15</subject><subject>Scanning electron microscopy</subject><subject>Solid state</subject><subject>Thermal stability</subject><subject>Thermogravimetric analysis</subject><issn>2073-4344</issn><issn>2073-4344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVkUuPEzEMx0cIJFbLHrlH4sosecwj4TZUC1QqLOJxHqWOU1JNJ90kg9SPwrfFpQhBcojj-P-zY1fVc8FvlTL8FdhiJ9FwwztpHlVXkveqblTTPP7Hflrd5LzntIxQWrRX1c8vpxnTLgC78x6hZBY9u08OEzr2AXM8xhSXzN4Ev8xQQpztxNZxJsEmPCzBvWYD-4xwgsluJ2SrcxmnXFiJbADAnNnqOx5ixono4Qeyj_WnFAtdKMF6dnEKM9bypaodwZENlCDuKOWz6om3U8abP-d19e3t3dfV-3pz_269GjY1SNOWGpTpjZJt2zUotFEdgEZhhWyxcd5hI7ZbSe-N5sZ0qpXGNV5b2HIvnOycuq7WF66Ldj8eUzjYdBqjDeNvR0y70aYSYMLRO20dSAWgqNO91671ZyzXirddb4n14sI6pviwYC7jPi6JfpRHJQSn6fRcUNTtJWpnCRpmH0uyQNvhIQA1wQfyD1rwXnCjWxLUFwGkmHNC_7dMwcfz9Mf_pq9-AbVWoow</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Siddan, Gouthaman</creator><creator>Solomon, Viswas Raja</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9863-4452</orcidid><orcidid>https://orcid.org/0000-0002-5530-8542</orcidid></search><sort><creationdate>20240901</creationdate><title>Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous</title><author>Siddan, Gouthaman ; Solomon, Viswas Raja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c295t-c3979325564e18936cc8e1a125e4dfde41bb23254809963529d4f8acb0f1d26d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adsorption</topic><topic>Alkylation</topic><topic>Carbon</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Chemical synthesis</topic><topic>Diketones</topic><topic>Fine chemicals</topic><topic>Green technology</topic><topic>heterogeneous catalyst</topic><topic>ionic liquid</topic><topic>Ionic liquids</topic><topic>mesoporous silica</topic><topic>Morphology</topic><topic>N-alkylated indoline-2,3-dione</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pore size</topic><topic>SBA-15</topic><topic>Scanning electron microscopy</topic><topic>Solid state</topic><topic>Thermal stability</topic><topic>Thermogravimetric analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Siddan, Gouthaman</creatorcontrib><creatorcontrib>Solomon, Viswas Raja</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Catalysts</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Siddan, Gouthaman</au><au>Solomon, Viswas Raja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous</atitle><jtitle>Catalysts</jtitle><date>2024-09-01</date><risdate>2024</risdate><volume>14</volume><issue>9</issue><spage>629</spage><pages>629-</pages><issn>2073-4344</issn><eissn>2073-4344</eissn><abstract>SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. 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subjects | Adsorption Alkylation Carbon Catalysts Catalytic activity Chemical synthesis Diketones Fine chemicals Green technology heterogeneous catalyst ionic liquid Ionic liquids mesoporous silica Morphology N-alkylated indoline-2,3-dione NMR Nuclear magnetic resonance Pore size SBA-15 Scanning electron microscopy Solid state Thermal stability Thermogravimetric analysis |
title | Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous |
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