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
Hauptverfasser: Nishida, Yoshihide, Sato, Katsutoshi, Chaudhari, Chandan, Yamada, Hiroshi, Toriyama, Takaaki, Yamamoto, Tomokazu, Matsumura, Syo, Aspera, Susan Meñez, Nakanishi, Hiroshi, Haneda, Masaaki, Nagaoka, Katsutoshi
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container_end_page 4137
container_issue 13
container_start_page 4128
container_title Catalysis science & technology
container_volume 12
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
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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. 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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 &amp; 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. 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2044-4761
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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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