Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles
Catalytic hydrogenation of nitriles is a cost-effective and green method for synthesizing amines and imines, which have many industrial applications. However, this reaction generally requires harsh reaction conditions and produces a mixture of amine and imine products due to its chemodiversity. Ther...
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Veröffentlicht in: | Catalysis science & technology 2022-07, Vol.12 (13), p.4128-4137 |
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creator | Nishida, Yoshihide Sato, Katsutoshi Chaudhari, Chandan Yamada, Hiroshi Toriyama, Takaaki Yamamoto, Tomokazu Matsumura, Syo Aspera, Susan Meñez Nakanishi, Hiroshi Haneda, Masaaki Nagaoka, Katsutoshi |
description | Catalytic hydrogenation of nitriles is a cost-effective and green method for synthesizing amines and imines, which have many industrial applications. However, this reaction generally requires harsh reaction conditions and produces a mixture of amine and imine products due to its chemodiversity. Therefore, it is a challenge to selectively hydrogenate nitriles to a single product under ambient conditions (1 bar of H
2
at 25 °C). Here, we report an effective method for selective hydrogenation of nitriles that does not require heat, pressurization, or long reaction times. We achieved this by means of bimetalization between palladium (Pd) and platinum (Pt) nanoparticles, which resulted in a catalyst that showed high yield of secondary amines. Although Pd and Pt are thermodynamically immiscible, we have successfully alloyed the two metals by means of rapid chemical reduction assisted by microwave heating. X-ray absorption spectroscopy suggested the formation of heteroatomic Pd
δ
+
Pt
δ
−
sites
via
charge transfer between neighboring Pd and Pt atoms in the alloy structure. Moreover, Fourier transform IR spectroscopy and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy indicated that decreasing the size of the PdPt (50 : 50) nanoparticles improved the degree of alloying and facilitated the formation of electron-enriched Pt
δ
−
species. On the basis of kinetics studies and density functional theory calculations, we concluded that cyano group activation, which was the rate-determining step over monometallic Pd and Pt catalysts, was accelerated over the heteroatomic Pd
δ
+
Pt
δ
−
sites because of strong back-donation from electron-enriched Pt
δ
−
species to the carbon atom of the cyano groups. The PdPt random alloy nanoparticles catalyzed the reactions of various aromatic and heterocyclic nitriles, and the corresponding secondary amines were selectively obtained in just a few hours.
Nitrile hydrogenation over PdPt random alloy nanoparticles. |
doi_str_mv | 10.1039/d1cy02302k |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_d1cy02302k</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2684177981</sourcerecordid><originalsourceid>FETCH-LOGICAL-c317t-e228bcc7826ba9e8ac44f1d3528fa51f54763e20e06c3b13b6c0470af59ca5743</originalsourceid><addsrcrecordid>eNpFkEtLxDAUhYMoOIyzcS8E3AnVvNqkSxkdFQfd6MJVSdNUM7ZJTVKh_96MI-Pd3NfHudwDwClGlxjR8qrBakKEIvJ5AGYEMZYxXuDDfZ3TY7AIYYNSsBIjQWZgfDLRm07Dj6nx7l1bGY2zMDoYtHK2kX6CsjdWBzjaRvvU1EbbCLdLs2UDdN9pPsiuk40Z-2zokoYde-ilbVwP08JN0ErrBumjUZ0OJ-ColV3Qi788B6-r25flfbZ-vntYXq8zRTGPmSZE1EpxQYpallpIxViLG5oT0coct3n6j2qCNCoUrTGtC4UYR7LNSyVzzugcnO90B---Rh1itXGjt-lkRQrBMOelwIm62FHKuxC8bqvBmz59XmFUbZ2tbvDy7dfZxwSf7WAf1J77d57-AFsmd-E</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2684177981</pqid></control><display><type>article</type><title>Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles</title><source>Royal Society Of Chemistry Journals</source><creator>Nishida, Yoshihide ; Sato, Katsutoshi ; Chaudhari, Chandan ; Yamada, Hiroshi ; Toriyama, Takaaki ; Yamamoto, Tomokazu ; Matsumura, Syo ; Aspera, Susan Meñez ; Nakanishi, Hiroshi ; Haneda, Masaaki ; Nagaoka, Katsutoshi</creator><creatorcontrib>Nishida, Yoshihide ; Sato, Katsutoshi ; Chaudhari, Chandan ; Yamada, Hiroshi ; Toriyama, Takaaki ; Yamamoto, Tomokazu ; Matsumura, Syo ; Aspera, Susan Meñez ; Nakanishi, Hiroshi ; Haneda, Masaaki ; Nagaoka, Katsutoshi</creatorcontrib><description>Catalytic hydrogenation of nitriles is a cost-effective and green method for synthesizing amines and imines, which have many industrial applications. However, this reaction generally requires harsh reaction conditions and produces a mixture of amine and imine products due to its chemodiversity. Therefore, it is a challenge to selectively hydrogenate nitriles to a single product under ambient conditions (1 bar of H
2
at 25 °C). Here, we report an effective method for selective hydrogenation of nitriles that does not require heat, pressurization, or long reaction times. We achieved this by means of bimetalization between palladium (Pd) and platinum (Pt) nanoparticles, which resulted in a catalyst that showed high yield of secondary amines. Although Pd and Pt are thermodynamically immiscible, we have successfully alloyed the two metals by means of rapid chemical reduction assisted by microwave heating. X-ray absorption spectroscopy suggested the formation of heteroatomic Pd
δ
+
Pt
δ
−
sites
via
charge transfer between neighboring Pd and Pt atoms in the alloy structure. Moreover, Fourier transform IR spectroscopy and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy indicated that decreasing the size of the PdPt (50 : 50) nanoparticles improved the degree of alloying and facilitated the formation of electron-enriched Pt
δ
−
species. On the basis of kinetics studies and density functional theory calculations, we concluded that cyano group activation, which was the rate-determining step over monometallic Pd and Pt catalysts, was accelerated over the heteroatomic Pd
δ
+
Pt
δ
−
sites because of strong back-donation from electron-enriched Pt
δ
−
species to the carbon atom of the cyano groups. The PdPt random alloy nanoparticles catalyzed the reactions of various aromatic and heterocyclic nitriles, and the corresponding secondary amines were selectively obtained in just a few hours.
Nitrile hydrogenation over PdPt random alloy nanoparticles.</description><identifier>ISSN: 2044-4753</identifier><identifier>EISSN: 2044-4761</identifier><identifier>DOI: 10.1039/d1cy02302k</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Alloying ; Amines ; Bimetals ; Catalysts ; Charge transfer ; Chemical reactions ; Chemical reduction ; Cyano groups ; Density functional theory ; Fourier transforms ; Hydrogenation ; Imines ; Industrial applications ; Infrared spectroscopy ; Nanoalloys ; Nanoparticles ; Nitriles ; Palladium ; Platinum ; Scanning transmission electron microscopy ; Spectrum analysis ; X ray absorption ; X-ray spectroscopy</subject><ispartof>Catalysis science & technology, 2022-07, Vol.12 (13), p.4128-4137</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-e228bcc7826ba9e8ac44f1d3528fa51f54763e20e06c3b13b6c0470af59ca5743</citedby><cites>FETCH-LOGICAL-c317t-e228bcc7826ba9e8ac44f1d3528fa51f54763e20e06c3b13b6c0470af59ca5743</cites><orcidid>0000-0001-9922-831X ; 0000-0003-1774-1537 ; 0000-0002-8842-1234 ; 0000-0002-3998-7012 ; 0000-0003-1040-348X ; 0000-0001-9843-1527</orcidid></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></links><search><creatorcontrib>Nishida, Yoshihide</creatorcontrib><creatorcontrib>Sato, Katsutoshi</creatorcontrib><creatorcontrib>Chaudhari, Chandan</creatorcontrib><creatorcontrib>Yamada, Hiroshi</creatorcontrib><creatorcontrib>Toriyama, Takaaki</creatorcontrib><creatorcontrib>Yamamoto, Tomokazu</creatorcontrib><creatorcontrib>Matsumura, Syo</creatorcontrib><creatorcontrib>Aspera, Susan Meñez</creatorcontrib><creatorcontrib>Nakanishi, Hiroshi</creatorcontrib><creatorcontrib>Haneda, Masaaki</creatorcontrib><creatorcontrib>Nagaoka, Katsutoshi</creatorcontrib><title>Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles</title><title>Catalysis science & technology</title><description>Catalytic hydrogenation of nitriles is a cost-effective and green method for synthesizing amines and imines, which have many industrial applications. However, this reaction generally requires harsh reaction conditions and produces a mixture of amine and imine products due to its chemodiversity. Therefore, it is a challenge to selectively hydrogenate nitriles to a single product under ambient conditions (1 bar of H
2
at 25 °C). Here, we report an effective method for selective hydrogenation of nitriles that does not require heat, pressurization, or long reaction times. We achieved this by means of bimetalization between palladium (Pd) and platinum (Pt) nanoparticles, which resulted in a catalyst that showed high yield of secondary amines. Although Pd and Pt are thermodynamically immiscible, we have successfully alloyed the two metals by means of rapid chemical reduction assisted by microwave heating. X-ray absorption spectroscopy suggested the formation of heteroatomic Pd
δ
+
Pt
δ
−
sites
via
charge transfer between neighboring Pd and Pt atoms in the alloy structure. Moreover, Fourier transform IR spectroscopy and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy indicated that decreasing the size of the PdPt (50 : 50) nanoparticles improved the degree of alloying and facilitated the formation of electron-enriched Pt
δ
−
species. On the basis of kinetics studies and density functional theory calculations, we concluded that cyano group activation, which was the rate-determining step over monometallic Pd and Pt catalysts, was accelerated over the heteroatomic Pd
δ
+
Pt
δ
−
sites because of strong back-donation from electron-enriched Pt
δ
−
species to the carbon atom of the cyano groups. The PdPt random alloy nanoparticles catalyzed the reactions of various aromatic and heterocyclic nitriles, and the corresponding secondary amines were selectively obtained in just a few hours.
Nitrile hydrogenation over PdPt random alloy nanoparticles.</description><subject>Alloying</subject><subject>Amines</subject><subject>Bimetals</subject><subject>Catalysts</subject><subject>Charge transfer</subject><subject>Chemical reactions</subject><subject>Chemical reduction</subject><subject>Cyano groups</subject><subject>Density functional theory</subject><subject>Fourier transforms</subject><subject>Hydrogenation</subject><subject>Imines</subject><subject>Industrial applications</subject><subject>Infrared spectroscopy</subject><subject>Nanoalloys</subject><subject>Nanoparticles</subject><subject>Nitriles</subject><subject>Palladium</subject><subject>Platinum</subject><subject>Scanning transmission electron microscopy</subject><subject>Spectrum analysis</subject><subject>X ray absorption</subject><subject>X-ray spectroscopy</subject><issn>2044-4753</issn><issn>2044-4761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLxDAUhYMoOIyzcS8E3AnVvNqkSxkdFQfd6MJVSdNUM7ZJTVKh_96MI-Pd3NfHudwDwClGlxjR8qrBakKEIvJ5AGYEMZYxXuDDfZ3TY7AIYYNSsBIjQWZgfDLRm07Dj6nx7l1bGY2zMDoYtHK2kX6CsjdWBzjaRvvU1EbbCLdLs2UDdN9pPsiuk40Z-2zokoYde-ilbVwP08JN0ErrBumjUZ0OJ-ColV3Qi788B6-r25flfbZ-vntYXq8zRTGPmSZE1EpxQYpallpIxViLG5oT0coct3n6j2qCNCoUrTGtC4UYR7LNSyVzzugcnO90B---Rh1itXGjt-lkRQrBMOelwIm62FHKuxC8bqvBmz59XmFUbZ2tbvDy7dfZxwSf7WAf1J77d57-AFsmd-E</recordid><startdate>20220704</startdate><enddate>20220704</enddate><creator>Nishida, Yoshihide</creator><creator>Sato, Katsutoshi</creator><creator>Chaudhari, Chandan</creator><creator>Yamada, Hiroshi</creator><creator>Toriyama, Takaaki</creator><creator>Yamamoto, Tomokazu</creator><creator>Matsumura, Syo</creator><creator>Aspera, Susan Meñez</creator><creator>Nakanishi, Hiroshi</creator><creator>Haneda, Masaaki</creator><creator>Nagaoka, Katsutoshi</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0001-9922-831X</orcidid><orcidid>https://orcid.org/0000-0003-1774-1537</orcidid><orcidid>https://orcid.org/0000-0002-8842-1234</orcidid><orcidid>https://orcid.org/0000-0002-3998-7012</orcidid><orcidid>https://orcid.org/0000-0003-1040-348X</orcidid><orcidid>https://orcid.org/0000-0001-9843-1527</orcidid></search><sort><creationdate>20220704</creationdate><title>Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles</title><author>Nishida, Yoshihide ; Sato, Katsutoshi ; Chaudhari, Chandan ; Yamada, Hiroshi ; Toriyama, Takaaki ; Yamamoto, Tomokazu ; Matsumura, Syo ; Aspera, Susan Meñez ; Nakanishi, Hiroshi ; Haneda, Masaaki ; Nagaoka, Katsutoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-e228bcc7826ba9e8ac44f1d3528fa51f54763e20e06c3b13b6c0470af59ca5743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alloying</topic><topic>Amines</topic><topic>Bimetals</topic><topic>Catalysts</topic><topic>Charge transfer</topic><topic>Chemical reactions</topic><topic>Chemical reduction</topic><topic>Cyano groups</topic><topic>Density functional theory</topic><topic>Fourier transforms</topic><topic>Hydrogenation</topic><topic>Imines</topic><topic>Industrial applications</topic><topic>Infrared spectroscopy</topic><topic>Nanoalloys</topic><topic>Nanoparticles</topic><topic>Nitriles</topic><topic>Palladium</topic><topic>Platinum</topic><topic>Scanning transmission electron microscopy</topic><topic>Spectrum analysis</topic><topic>X ray absorption</topic><topic>X-ray spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishida, Yoshihide</creatorcontrib><creatorcontrib>Sato, Katsutoshi</creatorcontrib><creatorcontrib>Chaudhari, Chandan</creatorcontrib><creatorcontrib>Yamada, Hiroshi</creatorcontrib><creatorcontrib>Toriyama, Takaaki</creatorcontrib><creatorcontrib>Yamamoto, Tomokazu</creatorcontrib><creatorcontrib>Matsumura, Syo</creatorcontrib><creatorcontrib>Aspera, Susan Meñez</creatorcontrib><creatorcontrib>Nakanishi, Hiroshi</creatorcontrib><creatorcontrib>Haneda, Masaaki</creatorcontrib><creatorcontrib>Nagaoka, Katsutoshi</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Catalysis science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishida, Yoshihide</au><au>Sato, Katsutoshi</au><au>Chaudhari, Chandan</au><au>Yamada, Hiroshi</au><au>Toriyama, Takaaki</au><au>Yamamoto, Tomokazu</au><au>Matsumura, Syo</au><au>Aspera, Susan Meñez</au><au>Nakanishi, Hiroshi</au><au>Haneda, Masaaki</au><au>Nagaoka, Katsutoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles</atitle><jtitle>Catalysis science & technology</jtitle><date>2022-07-04</date><risdate>2022</risdate><volume>12</volume><issue>13</issue><spage>4128</spage><epage>4137</epage><pages>4128-4137</pages><issn>2044-4753</issn><eissn>2044-4761</eissn><abstract>Catalytic hydrogenation of nitriles is a cost-effective and green method for synthesizing amines and imines, which have many industrial applications. However, this reaction generally requires harsh reaction conditions and produces a mixture of amine and imine products due to its chemodiversity. Therefore, it is a challenge to selectively hydrogenate nitriles to a single product under ambient conditions (1 bar of H
2
at 25 °C). Here, we report an effective method for selective hydrogenation of nitriles that does not require heat, pressurization, or long reaction times. We achieved this by means of bimetalization between palladium (Pd) and platinum (Pt) nanoparticles, which resulted in a catalyst that showed high yield of secondary amines. Although Pd and Pt are thermodynamically immiscible, we have successfully alloyed the two metals by means of rapid chemical reduction assisted by microwave heating. X-ray absorption spectroscopy suggested the formation of heteroatomic Pd
δ
+
Pt
δ
−
sites
via
charge transfer between neighboring Pd and Pt atoms in the alloy structure. Moreover, Fourier transform IR spectroscopy and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy indicated that decreasing the size of the PdPt (50 : 50) nanoparticles improved the degree of alloying and facilitated the formation of electron-enriched Pt
δ
−
species. On the basis of kinetics studies and density functional theory calculations, we concluded that cyano group activation, which was the rate-determining step over monometallic Pd and Pt catalysts, was accelerated over the heteroatomic Pd
δ
+
Pt
δ
−
sites because of strong back-donation from electron-enriched Pt
δ
−
species to the carbon atom of the cyano groups. The PdPt random alloy nanoparticles catalyzed the reactions of various aromatic and heterocyclic nitriles, and the corresponding secondary amines were selectively obtained in just a few hours.
Nitrile hydrogenation over PdPt random alloy nanoparticles.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1cy02302k</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9922-831X</orcidid><orcidid>https://orcid.org/0000-0003-1774-1537</orcidid><orcidid>https://orcid.org/0000-0002-8842-1234</orcidid><orcidid>https://orcid.org/0000-0002-3998-7012</orcidid><orcidid>https://orcid.org/0000-0003-1040-348X</orcidid><orcidid>https://orcid.org/0000-0001-9843-1527</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals |
subjects | Alloying Amines Bimetals Catalysts Charge transfer Chemical reactions Chemical reduction Cyano groups Density functional theory Fourier transforms Hydrogenation Imines Industrial applications Infrared spectroscopy Nanoalloys Nanoparticles Nitriles Palladium Platinum Scanning transmission electron microscopy Spectrum analysis X ray absorption X-ray spectroscopy |
title | Nitrile hydrogenation to secondary amines under ambient conditions over palladium-platinum random alloy nanoparticles |
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