Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium
Functionalized flower-like mesoporous silica with a chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-((trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediami n e and tetraethoxysilane under a cooperative dual-template app...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2013-01, Vol.15 (8), p.2208-2214 |
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creator | Gao, Fei Jin, Ronghua Zhang, Dacheng Liang, Quanxi Ye, Qunqun Liu, Guohua |
description | Functionalized flower-like mesoporous silica with a chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-((trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediami n e and tetraethoxysilane under a cooperative dual-template approach followed by complexation with organorhodium complexes. Structural characterization discloses its mesostructure and well-defined single-site chiral organorhodium functionality, while electron microscopy analyses reveal the uniformly distributed three-dimensional spherical flowers constructed by the stacking of leaf-shaped nanoflakes. In particular, as a bifunctionalized heterogeneous catalyst, it shows excellent catalytic activity and high enantioselectivity in the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium (more than 99% conversion and up to 97% ee). The superior catalytic performance is attributed to the synergistic effect of the salient cetyltrimethylammonium bromide phase-transfer function and confined chiral organorhodium catalytic nature. Furthermore, this heterogeneous catalyst could be recovered easily and reused repeatedly (ten times) without affecting its ee value, showing a practical application in asymmetric synthesis. |
doi_str_mv | 10.1039/c3gc40547h |
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Structural characterization discloses its mesostructure and well-defined single-site chiral organorhodium functionality, while electron microscopy analyses reveal the uniformly distributed three-dimensional spherical flowers constructed by the stacking of leaf-shaped nanoflakes. In particular, as a bifunctionalized heterogeneous catalyst, it shows excellent catalytic activity and high enantioselectivity in the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium (more than 99% conversion and up to 97% ee). The superior catalytic performance is attributed to the synergistic effect of the salient cetyltrimethylammonium bromide phase-transfer function and confined chiral organorhodium catalytic nature. Furthermore, this heterogeneous catalyst could be recovered easily and reused repeatedly (ten times) without affecting its ee value, showing a practical application in asymmetric synthesis.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c3gc40547h</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Asymmetry ; Catalysis ; Catalysts ; Catalysts: preparations and properties ; Chemistry ; Condensed benzenic and aromatic compounds ; Exact sciences and technology ; General and physical chemistry ; Hydrogenation ; Ketones ; Nanostructure ; Noncondensed benzenic compounds ; Organic chemistry ; Preparations and properties ; Silicon dioxide ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Three dimensional</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2013-01, Vol.15 (8), p.2208-2214</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c364t-b5c4ea9a3f0d7bc658eceda3f6b8e1202d0b2b441a986cdf477c4991e2729cab3</citedby><cites>FETCH-LOGICAL-c364t-b5c4ea9a3f0d7bc658eceda3f6b8e1202d0b2b441a986cdf477c4991e2729cab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27605838$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Fei</creatorcontrib><creatorcontrib>Jin, Ronghua</creatorcontrib><creatorcontrib>Zhang, Dacheng</creatorcontrib><creatorcontrib>Liang, Quanxi</creatorcontrib><creatorcontrib>Ye, Qunqun</creatorcontrib><creatorcontrib>Liu, Guohua</creatorcontrib><title>Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Functionalized flower-like mesoporous silica with a chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-((trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediami n e and tetraethoxysilane under a cooperative dual-template approach followed by complexation with organorhodium complexes. Structural characterization discloses its mesostructure and well-defined single-site chiral organorhodium functionality, while electron microscopy analyses reveal the uniformly distributed three-dimensional spherical flowers constructed by the stacking of leaf-shaped nanoflakes. In particular, as a bifunctionalized heterogeneous catalyst, it shows excellent catalytic activity and high enantioselectivity in the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium (more than 99% conversion and up to 97% ee). The superior catalytic performance is attributed to the synergistic effect of the salient cetyltrimethylammonium bromide phase-transfer function and confined chiral organorhodium catalytic nature. Furthermore, this heterogeneous catalyst could be recovered easily and reused repeatedly (ten times) without affecting its ee value, showing a practical application in asymmetric synthesis.</description><subject>Asymmetry</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Condensed benzenic and aromatic compounds</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hydrogenation</subject><subject>Ketones</subject><subject>Nanostructure</subject><subject>Noncondensed benzenic compounds</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Silicon dioxide</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>Three dimensional</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Fei</creatorcontrib><creatorcontrib>Jin, Ronghua</creatorcontrib><creatorcontrib>Zhang, Dacheng</creatorcontrib><creatorcontrib>Liang, Quanxi</creatorcontrib><creatorcontrib>Ye, Qunqun</creatorcontrib><creatorcontrib>Liu, Guohua</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Fei</au><au>Jin, Ronghua</au><au>Zhang, Dacheng</au><au>Liang, Quanxi</au><au>Ye, Qunqun</au><au>Liu, Guohua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>15</volume><issue>8</issue><spage>2208</spage><epage>2214</epage><pages>2208-2214</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Functionalized flower-like mesoporous silica with a chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-((trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediami n e and tetraethoxysilane under a cooperative dual-template approach followed by complexation with organorhodium complexes. Structural characterization discloses its mesostructure and well-defined single-site chiral organorhodium functionality, while electron microscopy analyses reveal the uniformly distributed three-dimensional spherical flowers constructed by the stacking of leaf-shaped nanoflakes. In particular, as a bifunctionalized heterogeneous catalyst, it shows excellent catalytic activity and high enantioselectivity in the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium (more than 99% conversion and up to 97% ee). The superior catalytic performance is attributed to the synergistic effect of the salient cetyltrimethylammonium bromide phase-transfer function and confined chiral organorhodium catalytic nature. 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subjects | Asymmetry Catalysis Catalysts Catalysts: preparations and properties Chemistry Condensed benzenic and aromatic compounds Exact sciences and technology General and physical chemistry Hydrogenation Ketones Nanostructure Noncondensed benzenic compounds Organic chemistry Preparations and properties Silicon dioxide Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry Three dimensional |
title | Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium |
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