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Anchoring of Copper Complex in MCM-41 Matrix: A Highly Efficient Catalyst for Epoxidation of Olefins by tert-BuOOH
A complex moiety containing copper (II) has been anchored covalently into the organic-modified Si−MCM-41 to prepare a new catalyst. The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si−MCM-41 via silicon alkoxide route. The amine group...
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Published in: | Langmuir 2007-02, Vol.23 (5), p.2492-2496 |
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creator | Jana, Sreyashi Dutta, Buddhadeb Bera, Rajesh Koner, Subratanath |
description | A complex moiety containing copper (II) has been anchored covalently into the organic-modified Si−MCM-41 to prepare a new catalyst. The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si−MCM-41 via silicon alkoxide route. The amine group upon condensation with salicyldehyde affords a bidentate ligand in the mesoporous matrix for anchoring copper(II) ions. The prepared catalyst has been characterized by UV−vis, electron paramagnetic resonance (EPR), and infrared (IR) spectroscopic analysis, small-angle X-ray diffraction, and N2 sorption study. A remarkable difference in the pore structure has been observed after the immobilization of copper(II) complex in Si−MCM-41. The catalyst showed excellent catalytic efficiency in epoxidation reactions with various olefinic compounds including styrene and allyl alcohol, using tert-BuOOH as oxidant. Notably, styrene shows unprecedented high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH over the Cu−MCM-41 catalyst. |
doi_str_mv | 10.1021/la062409t |
format | article |
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The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si−MCM-41 via silicon alkoxide route. The amine group upon condensation with salicyldehyde affords a bidentate ligand in the mesoporous matrix for anchoring copper(II) ions. The prepared catalyst has been characterized by UV−vis, electron paramagnetic resonance (EPR), and infrared (IR) spectroscopic analysis, small-angle X-ray diffraction, and N2 sorption study. A remarkable difference in the pore structure has been observed after the immobilization of copper(II) complex in Si−MCM-41. The catalyst showed excellent catalytic efficiency in epoxidation reactions with various olefinic compounds including styrene and allyl alcohol, using tert-BuOOH as oxidant. Notably, styrene shows unprecedented high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH over the Cu−MCM-41 catalyst.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la062409t</identifier><identifier>PMID: 17309205</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Catalysis ; Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; Porous materials ; Surface physical chemistry ; Theory of reactions, general kinetics. Catalysis. 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The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si−MCM-41 via silicon alkoxide route. The amine group upon condensation with salicyldehyde affords a bidentate ligand in the mesoporous matrix for anchoring copper(II) ions. The prepared catalyst has been characterized by UV−vis, electron paramagnetic resonance (EPR), and infrared (IR) spectroscopic analysis, small-angle X-ray diffraction, and N2 sorption study. A remarkable difference in the pore structure has been observed after the immobilization of copper(II) complex in Si−MCM-41. The catalyst showed excellent catalytic efficiency in epoxidation reactions with various olefinic compounds including styrene and allyl alcohol, using tert-BuOOH as oxidant. Notably, styrene shows unprecedented high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH over the Cu−MCM-41 catalyst.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Porous materials</subject><subject>Surface physical chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jana, Sreyashi</creatorcontrib><creatorcontrib>Dutta, Buddhadeb</creatorcontrib><creatorcontrib>Bera, Rajesh</creatorcontrib><creatorcontrib>Koner, Subratanath</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jana, Sreyashi</au><au>Dutta, Buddhadeb</au><au>Bera, Rajesh</au><au>Koner, Subratanath</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anchoring of Copper Complex in MCM-41 Matrix: A Highly Efficient Catalyst for Epoxidation of Olefins by tert-BuOOH</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2007-02-27</date><risdate>2007</risdate><volume>23</volume><issue>5</issue><spage>2492</spage><epage>2496</epage><pages>2492-2496</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>A complex moiety containing copper (II) has been anchored covalently into the organic-modified Si−MCM-41 to prepare a new catalyst. The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si−MCM-41 via silicon alkoxide route. The amine group upon condensation with salicyldehyde affords a bidentate ligand in the mesoporous matrix for anchoring copper(II) ions. The prepared catalyst has been characterized by UV−vis, electron paramagnetic resonance (EPR), and infrared (IR) spectroscopic analysis, small-angle X-ray diffraction, and N2 sorption study. A remarkable difference in the pore structure has been observed after the immobilization of copper(II) complex in Si−MCM-41. The catalyst showed excellent catalytic efficiency in epoxidation reactions with various olefinic compounds including styrene and allyl alcohol, using tert-BuOOH as oxidant. Notably, styrene shows unprecedented high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH over the Cu−MCM-41 catalyst.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17309205</pmid><doi>10.1021/la062409t</doi><tpages>5</tpages></addata></record> |
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subjects | Catalysis Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry Porous materials Surface physical chemistry Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Anchoring of Copper Complex in MCM-41 Matrix: A Highly Efficient Catalyst for Epoxidation of Olefins by tert-BuOOH |
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