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Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction
Immobilization of palladium nanoparticles onto the fluorine-doped tin oxide (FTO) as support Pd/FTO, resulted in a highly active heterogeneous catalyst for Suzuki-Miyaura cross-coupling reactions and 4-nitrophenol reduction. The Pd/FTO catalyst has been synthesized by immobilization of palladium nan...
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Published in: | Journal of chemical sciences (Bangalore, India) India), 2019-11, Vol.131 (11), p.1-12, Article 111 |
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container_title | Journal of chemical sciences (Bangalore, India) |
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creator | Mak, Sek Yin Liew, Kin Hong Chua, Chia Chia Yarmo, Mohd Ambar Yahaya, Badrul H Samad, Wan Zurina Jamil, Mohd Suzeren Md Yusop, Rahimi M |
description | Immobilization of palladium nanoparticles onto the fluorine-doped tin oxide (FTO) as support Pd/FTO, resulted in a highly active heterogeneous catalyst for Suzuki-Miyaura cross-coupling reactions and 4-nitrophenol reduction. The Pd/FTO catalyst has been synthesized by immobilization of palladium nanoparticles onto FTO
via
a simple impregnation method. ICP-MS analysis confirmed that there is 0.11 mmol/g of palladium was loaded successfully on FTO support. The crystallinity, morphologies, compositions and surface properties of Pd/FTO were fully characterized by various techniques. It was further examined for its catalytic activity and robustness in Suzuki coupling reaction with different aryl halides and solvents. The yields obtained from Suzuki coupling reactions were basically over 80%. The prepared catalyst was also tested on mild reaction such as reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Pd/FTO catalyst exhibited high catalytic activity towards 4-NP reduction with a rate constant of 1.776 min
−1
and turnover frequency (TOF) value of 29.1 hr
−1
. The findings revealed that Pd/FTO also maintained its high stability for five consecutive runs in Suzuki reactions and 4-NP reductions. The catalyst showed excellent catalytic activities by using a small amount of Pd/FTO for the Suzuki coupling reaction and 4-NP reduction.
Graphic abstract
Novel Pd-supported FTO nano-powder catalyst exhibited high activity and selectivity towards C-C Suzuki coupling reaction and nitroarene reduction. |
doi_str_mv | 10.1007/s12039-019-1685-7 |
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via
a simple impregnation method. ICP-MS analysis confirmed that there is 0.11 mmol/g of palladium was loaded successfully on FTO support. The crystallinity, morphologies, compositions and surface properties of Pd/FTO were fully characterized by various techniques. It was further examined for its catalytic activity and robustness in Suzuki coupling reaction with different aryl halides and solvents. The yields obtained from Suzuki coupling reactions were basically over 80%. The prepared catalyst was also tested on mild reaction such as reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Pd/FTO catalyst exhibited high catalytic activity towards 4-NP reduction with a rate constant of 1.776 min
−1
and turnover frequency (TOF) value of 29.1 hr
−1
. The findings revealed that Pd/FTO also maintained its high stability for five consecutive runs in Suzuki reactions and 4-NP reductions. The catalyst showed excellent catalytic activities by using a small amount of Pd/FTO for the Suzuki coupling reaction and 4-NP reduction.
Graphic abstract
Novel Pd-supported FTO nano-powder catalyst exhibited high activity and selectivity towards C-C Suzuki coupling reaction and nitroarene reduction.</description><identifier>ISSN: 0974-3626</identifier><identifier>EISSN: 0973-7103</identifier><identifier>DOI: 10.1007/s12039-019-1685-7</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Aminophenol ; Aromatic compounds ; Catalysts ; Catalytic activity ; Chemical bonds ; Chemical industry ; Chemical reactions ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Cross coupling ; Fluorine ; Halides ; Immobilization ; Morphology ; Nanoparticles ; Nitrophenol ; Palladium ; Reduction ; Regular Article ; Selectivity ; Surface properties ; Tin oxides</subject><ispartof>Journal of chemical sciences (Bangalore, India), 2019-11, Vol.131 (11), p.1-12, Article 111</ispartof><rights>Indian Academy of Sciences 2019</rights><rights>Copyright Springer Nature B.V. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-5f2f1c6256e8abd47ddc65f38aaa2da0aad9590289aef1c1658b801cc070e0c13</citedby><cites>FETCH-LOGICAL-c359t-5f2f1c6256e8abd47ddc65f38aaa2da0aad9590289aef1c1658b801cc070e0c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids></links><search><creatorcontrib>Mak, Sek Yin</creatorcontrib><creatorcontrib>Liew, Kin Hong</creatorcontrib><creatorcontrib>Chua, Chia Chia</creatorcontrib><creatorcontrib>Yarmo, Mohd Ambar</creatorcontrib><creatorcontrib>Yahaya, Badrul H</creatorcontrib><creatorcontrib>Samad, Wan Zurina</creatorcontrib><creatorcontrib>Jamil, Mohd Suzeren Md</creatorcontrib><creatorcontrib>Yusop, Rahimi M</creatorcontrib><title>Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction</title><title>Journal of chemical sciences (Bangalore, India)</title><addtitle>J Chem Sci</addtitle><description>Immobilization of palladium nanoparticles onto the fluorine-doped tin oxide (FTO) as support Pd/FTO, resulted in a highly active heterogeneous catalyst for Suzuki-Miyaura cross-coupling reactions and 4-nitrophenol reduction. The Pd/FTO catalyst has been synthesized by immobilization of palladium nanoparticles onto FTO
via
a simple impregnation method. ICP-MS analysis confirmed that there is 0.11 mmol/g of palladium was loaded successfully on FTO support. The crystallinity, morphologies, compositions and surface properties of Pd/FTO were fully characterized by various techniques. It was further examined for its catalytic activity and robustness in Suzuki coupling reaction with different aryl halides and solvents. The yields obtained from Suzuki coupling reactions were basically over 80%. The prepared catalyst was also tested on mild reaction such as reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Pd/FTO catalyst exhibited high catalytic activity towards 4-NP reduction with a rate constant of 1.776 min
−1
and turnover frequency (TOF) value of 29.1 hr
−1
. The findings revealed that Pd/FTO also maintained its high stability for five consecutive runs in Suzuki reactions and 4-NP reductions. The catalyst showed excellent catalytic activities by using a small amount of Pd/FTO for the Suzuki coupling reaction and 4-NP reduction.
Graphic abstract
Novel Pd-supported FTO nano-powder catalyst exhibited high activity and selectivity towards C-C Suzuki coupling reaction and nitroarene reduction.</description><subject>Aminophenol</subject><subject>Aromatic compounds</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemical bonds</subject><subject>Chemical industry</subject><subject>Chemical reactions</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Cross coupling</subject><subject>Fluorine</subject><subject>Halides</subject><subject>Immobilization</subject><subject>Morphology</subject><subject>Nanoparticles</subject><subject>Nitrophenol</subject><subject>Palladium</subject><subject>Reduction</subject><subject>Regular Article</subject><subject>Selectivity</subject><subject>Surface properties</subject><subject>Tin oxides</subject><issn>0974-3626</issn><issn>0973-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKxTAQhosoeH0AdwHX0aQ5TdqliDcQFNR1GJPJMVqTmguoz-EDWz2CK1czDN__D3xNs8_ZIWdMHWXeMjFQxgfKZd9RtdZssUEJqjgT6z_7ggrZys1mO-cnxkS_UGKr-byBcQTr6wsJEOIEqXgzYia5TlNMBS2JgbixxuQDUhun-VJ8IPHNWySQCQSCznnjMRTyiAVTXGLAWDMxUGB8z4W4mMht_ajPnphYp9GH5ZyzZEGDLylOjxjiSBLaaoqPYbfZcDBm3PudO8392endyQW9uj6_PDm-okZ0Q6Gdax03su0k9vBgF8paIzsnegBoLTAAO3QDa_sBcAa57PqHnnFjmGLIDBc7zcGqd0rxtWIu-inWFOaXuhVccCnV0M0UX1EmxZwTOj0l_wLpXXOmv-XrlXw9y9ff8rWaM-0qk2c2LDH9Nf8f-gJZLYvW</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Mak, Sek Yin</creator><creator>Liew, Kin Hong</creator><creator>Chua, Chia Chia</creator><creator>Yarmo, Mohd Ambar</creator><creator>Yahaya, Badrul H</creator><creator>Samad, Wan Zurina</creator><creator>Jamil, Mohd Suzeren Md</creator><creator>Yusop, Rahimi M</creator><general>Springer India</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20191101</creationdate><title>Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction</title><author>Mak, Sek Yin ; Liew, Kin Hong ; Chua, Chia Chia ; Yarmo, Mohd Ambar ; Yahaya, Badrul H ; Samad, Wan Zurina ; Jamil, Mohd Suzeren Md ; Yusop, Rahimi M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-5f2f1c6256e8abd47ddc65f38aaa2da0aad9590289aef1c1658b801cc070e0c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aminophenol</topic><topic>Aromatic compounds</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Chemical bonds</topic><topic>Chemical industry</topic><topic>Chemical reactions</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Cross coupling</topic><topic>Fluorine</topic><topic>Halides</topic><topic>Immobilization</topic><topic>Morphology</topic><topic>Nanoparticles</topic><topic>Nitrophenol</topic><topic>Palladium</topic><topic>Reduction</topic><topic>Regular Article</topic><topic>Selectivity</topic><topic>Surface properties</topic><topic>Tin oxides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mak, Sek Yin</creatorcontrib><creatorcontrib>Liew, Kin Hong</creatorcontrib><creatorcontrib>Chua, Chia Chia</creatorcontrib><creatorcontrib>Yarmo, Mohd Ambar</creatorcontrib><creatorcontrib>Yahaya, Badrul H</creatorcontrib><creatorcontrib>Samad, Wan Zurina</creatorcontrib><creatorcontrib>Jamil, Mohd Suzeren Md</creatorcontrib><creatorcontrib>Yusop, Rahimi M</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of chemical sciences (Bangalore, India)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mak, Sek Yin</au><au>Liew, Kin Hong</au><au>Chua, Chia Chia</au><au>Yarmo, Mohd Ambar</au><au>Yahaya, Badrul H</au><au>Samad, Wan Zurina</au><au>Jamil, Mohd Suzeren Md</au><au>Yusop, Rahimi M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction</atitle><jtitle>Journal of chemical sciences (Bangalore, India)</jtitle><stitle>J Chem Sci</stitle><date>2019-11-01</date><risdate>2019</risdate><volume>131</volume><issue>11</issue><spage>1</spage><epage>12</epage><pages>1-12</pages><artnum>111</artnum><issn>0974-3626</issn><eissn>0973-7103</eissn><abstract>Immobilization of palladium nanoparticles onto the fluorine-doped tin oxide (FTO) as support Pd/FTO, resulted in a highly active heterogeneous catalyst for Suzuki-Miyaura cross-coupling reactions and 4-nitrophenol reduction. The Pd/FTO catalyst has been synthesized by immobilization of palladium nanoparticles onto FTO
via
a simple impregnation method. ICP-MS analysis confirmed that there is 0.11 mmol/g of palladium was loaded successfully on FTO support. The crystallinity, morphologies, compositions and surface properties of Pd/FTO were fully characterized by various techniques. It was further examined for its catalytic activity and robustness in Suzuki coupling reaction with different aryl halides and solvents. The yields obtained from Suzuki coupling reactions were basically over 80%. The prepared catalyst was also tested on mild reaction such as reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Pd/FTO catalyst exhibited high catalytic activity towards 4-NP reduction with a rate constant of 1.776 min
−1
and turnover frequency (TOF) value of 29.1 hr
−1
. The findings revealed that Pd/FTO also maintained its high stability for five consecutive runs in Suzuki reactions and 4-NP reductions. The catalyst showed excellent catalytic activities by using a small amount of Pd/FTO for the Suzuki coupling reaction and 4-NP reduction.
Graphic abstract
Novel Pd-supported FTO nano-powder catalyst exhibited high activity and selectivity towards C-C Suzuki coupling reaction and nitroarene reduction.</abstract><cop>New Delhi</cop><pub>Springer India</pub><doi>10.1007/s12039-019-1685-7</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aminophenol Aromatic compounds Catalysts Catalytic activity Chemical bonds Chemical industry Chemical reactions Chemical synthesis Chemistry Chemistry and Materials Science Chemistry/Food Science Cross coupling Fluorine Halides Immobilization Morphology Nanoparticles Nitrophenol Palladium Reduction Regular Article Selectivity Surface properties Tin oxides |
title | Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction |
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