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Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins
Gold nanoparticles were deposited directly onto ion-exchange resins by reducing HAuCl 4 or Au(en) 2Cl 3, exclusively on the resin surfaces. Gold nanoparticles deposited on a strongly basic anion-exchange resin exhibited high catalytic activity for glucose oxidation with a TOF as high as 27,000 h −1...
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Published in: | Applied catalysis. A, General General, 2009-02, Vol.353 (2), p.243-248 |
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creator | Ishida, Tamao Okamoto, Shinpei Makiyama, Risa Haruta, Masatake |
description | Gold nanoparticles were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3, exclusively on the resin surfaces. Gold nanoparticles deposited on a strongly basic anion-exchange resin exhibited high catalytic activity for glucose oxidation with a TOF as high as 27,000
h
−1 at 60
°C and at pH 9.5.
Anion-exchange resin supported Au nanoparticles also catalyzed the oxidation of 1-phenylethanol under base-free conditions.
▪
Gold nanoparticles (Au NPs) were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3 (en
=
ethylenediamine) with NaBH
4 or with surface amine and ammonium groups in anion-exchange resins. Catalytic activity for the oxidation of glucose and of 1-phenylethanol with molecular oxygen was more greatly influenced by the nature of polymer supports than by the size of Au NPs and increased in the order of the basicity of ion-exchange resins. Strongly basic anion-exchange resins such as quaternary ammonium salt (–N
+Me
3) functionalized resin exhibited a TOF (the reaction rate per loaded Au) as high as 27,000
h
−1 (7.5
s
−1) for glucose oxidation at 60
°C and at pH 9.5. For 1-phenylethanol under base-free conditions, a TOF of 60
h
−1 was obtained at 60
°C, indicating that anion-exchange resins worked as solid bases. |
doi_str_mv | 10.1016/j.apcata.2008.10.049 |
format | article |
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4 or Au(en)
2Cl
3, exclusively on the resin surfaces. Gold nanoparticles deposited on a strongly basic anion-exchange resin exhibited high catalytic activity for glucose oxidation with a TOF as high as 27,000
h
−1 at 60
°C and at pH 9.5.
Anion-exchange resin supported Au nanoparticles also catalyzed the oxidation of 1-phenylethanol under base-free conditions.
▪
Gold nanoparticles (Au NPs) were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3 (en
=
ethylenediamine) with NaBH
4 or with surface amine and ammonium groups in anion-exchange resins. Catalytic activity for the oxidation of glucose and of 1-phenylethanol with molecular oxygen was more greatly influenced by the nature of polymer supports than by the size of Au NPs and increased in the order of the basicity of ion-exchange resins. Strongly basic anion-exchange resins such as quaternary ammonium salt (–N
+Me
3) functionalized resin exhibited a TOF (the reaction rate per loaded Au) as high as 27,000
h
−1 (7.5
s
−1) for glucose oxidation at 60
°C and at pH 9.5. For 1-phenylethanol under base-free conditions, a TOF of 60
h
−1 was obtained at 60
°C, indicating that anion-exchange resins worked as solid bases.</description><identifier>ISSN: 0926-860X</identifier><identifier>EISSN: 1873-3875</identifier><identifier>DOI: 10.1016/j.apcata.2008.10.049</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Alcohol oxidation ; Catalysis ; Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; Glucose oxidation ; Gold catalyst ; Gold nanoparticles ; Ion-exchange resin ; Physical and chemical studies. Granulometry. Electrokinetic phenomena ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Applied catalysis. A, General, 2009-02, Vol.353 (2), p.243-248</ispartof><rights>2008 Elsevier B.V.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-efa927fb4ec68479e7178473be8efb7664f670364486f805e4e941c6a3b3197a3</citedby><cites>FETCH-LOGICAL-c433t-efa927fb4ec68479e7178473be8efb7664f670364486f805e4e941c6a3b3197a3</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=21073198$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishida, Tamao</creatorcontrib><creatorcontrib>Okamoto, Shinpei</creatorcontrib><creatorcontrib>Makiyama, Risa</creatorcontrib><creatorcontrib>Haruta, Masatake</creatorcontrib><title>Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins</title><title>Applied catalysis. A, General</title><description>Gold nanoparticles were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3, exclusively on the resin surfaces. Gold nanoparticles deposited on a strongly basic anion-exchange resin exhibited high catalytic activity for glucose oxidation with a TOF as high as 27,000
h
−1 at 60
°C and at pH 9.5.
Anion-exchange resin supported Au nanoparticles also catalyzed the oxidation of 1-phenylethanol under base-free conditions.
▪
Gold nanoparticles (Au NPs) were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3 (en
=
ethylenediamine) with NaBH
4 or with surface amine and ammonium groups in anion-exchange resins. Catalytic activity for the oxidation of glucose and of 1-phenylethanol with molecular oxygen was more greatly influenced by the nature of polymer supports than by the size of Au NPs and increased in the order of the basicity of ion-exchange resins. Strongly basic anion-exchange resins such as quaternary ammonium salt (–N
+Me
3) functionalized resin exhibited a TOF (the reaction rate per loaded Au) as high as 27,000
h
−1 (7.5
s
−1) for glucose oxidation at 60
°C and at pH 9.5. For 1-phenylethanol under base-free conditions, a TOF of 60
h
−1 was obtained at 60
°C, indicating that anion-exchange resins worked as solid bases.</description><subject>Alcohol oxidation</subject><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>Glucose oxidation</subject><subject>Gold catalyst</subject><subject>Gold nanoparticles</subject><subject>Ion-exchange resin</subject><subject>Physical and chemical studies. Granulometry. Electrokinetic phenomena</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0926-860X</issn><issn>1873-3875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kEFrGzEQhUVpoa6bf5CDLu1tHWklS9pLwZimLQRySSA3odWOHBlZ2kprY__7yGzosadhhvfezHwI3VKyooSKu_3KjNZMZtUSoupoRXj3AS2okqxhSq4_ogXpWtEoQV4-oy-l7AkhLe_WC5Q3kFPvLU5nP5jJp4iTw7twtKkANnHAtBlfIV4CTK8mpoDTCTLepTDgWPvR5MnbAAUPPoOdwgUPMKbiJxhwDauBDZxtte4AZyg-lq_okzOhwM17XaLn-59P29_Nw-OvP9vNQ2M5Y1MDznStdD0HKxSXHUgqa2U9KHC9FII7IQkTnCvhFFkDh45TKwzrGe2kYUv0fc4dc_p7hDLpgy8WQjAR0rFo1iohRUeqkM9Cm1MpGZwesz-YfNGU6CtgvdczYH0FfJ1WwNX27T3fFGuCyyZaX_55W0pkPURV3Y9ZB_XZk4esi_UQLczE9JD8_xe9AX9HlNw</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Ishida, Tamao</creator><creator>Okamoto, Shinpei</creator><creator>Makiyama, Risa</creator><creator>Haruta, Masatake</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20090201</creationdate><title>Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins</title><author>Ishida, Tamao ; Okamoto, Shinpei ; Makiyama, Risa ; Haruta, Masatake</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-efa927fb4ec68479e7178473be8efb7664f670364486f805e4e941c6a3b3197a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Alcohol oxidation</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Glucose oxidation</topic><topic>Gold catalyst</topic><topic>Gold nanoparticles</topic><topic>Ion-exchange resin</topic><topic>Physical and chemical studies. Granulometry. Electrokinetic phenomena</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishida, Tamao</creatorcontrib><creatorcontrib>Okamoto, Shinpei</creatorcontrib><creatorcontrib>Makiyama, Risa</creatorcontrib><creatorcontrib>Haruta, Masatake</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>Applied catalysis. A, General</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishida, Tamao</au><au>Okamoto, Shinpei</au><au>Makiyama, Risa</au><au>Haruta, Masatake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins</atitle><jtitle>Applied catalysis. A, General</jtitle><date>2009-02-01</date><risdate>2009</risdate><volume>353</volume><issue>2</issue><spage>243</spage><epage>248</epage><pages>243-248</pages><issn>0926-860X</issn><eissn>1873-3875</eissn><abstract>Gold nanoparticles were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3, exclusively on the resin surfaces. Gold nanoparticles deposited on a strongly basic anion-exchange resin exhibited high catalytic activity for glucose oxidation with a TOF as high as 27,000
h
−1 at 60
°C and at pH 9.5.
Anion-exchange resin supported Au nanoparticles also catalyzed the oxidation of 1-phenylethanol under base-free conditions.
▪
Gold nanoparticles (Au NPs) were deposited directly onto ion-exchange resins by reducing HAuCl
4 or Au(en)
2Cl
3 (en
=
ethylenediamine) with NaBH
4 or with surface amine and ammonium groups in anion-exchange resins. Catalytic activity for the oxidation of glucose and of 1-phenylethanol with molecular oxygen was more greatly influenced by the nature of polymer supports than by the size of Au NPs and increased in the order of the basicity of ion-exchange resins. Strongly basic anion-exchange resins such as quaternary ammonium salt (–N
+Me
3) functionalized resin exhibited a TOF (the reaction rate per loaded Au) as high as 27,000
h
−1 (7.5
s
−1) for glucose oxidation at 60
°C and at pH 9.5. For 1-phenylethanol under base-free conditions, a TOF of 60
h
−1 was obtained at 60
°C, indicating that anion-exchange resins worked as solid bases.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcata.2008.10.049</doi><tpages>6</tpages></addata></record> |
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source | ScienceDirect Journals |
subjects | Alcohol oxidation Catalysis Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry Glucose oxidation Gold catalyst Gold nanoparticles Ion-exchange resin Physical and chemical studies. Granulometry. Electrokinetic phenomena Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins |
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