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Controlled Shell and Kernel Modifications of Atomically Precise Pd/Ag Superatomic Nanoclusters

The first 8‐electron Pd/Ag superatomic alloys with an interstitial hydride [PdHAg19(dtp)12] (dtp=S2P(OiPr)2−) 1 and [PdHAg20(dtp)12]+ 2 are reported. The targeted addition of a single Ag atom to 1 is achieved by the reaction of one equivalent of trifluoroacetic acid, resulting in the formation of 2...

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Published in:Chemistry : a European journal 2023-06, Vol.29 (31), p.e202300730-n/a
Main Authors: Ni, Yu‐Rong, Pillay, Michael N., Chiu, Tzu‐Hao, Wu, Ying‐Yann, Kahlal, Samia, Saillard, Jean‐Yves, Liu, C. W.
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description The first 8‐electron Pd/Ag superatomic alloys with an interstitial hydride [PdHAg19(dtp)12] (dtp=S2P(OiPr)2−) 1 and [PdHAg20(dtp)12]+ 2 are reported. The targeted addition of a single Ag atom to 1 is achieved by the reaction of one equivalent of trifluoroacetic acid, resulting in the formation of 2 in 55 % yield. Further modification of the shell results in the formation of [PdAg21(dtp)12]+ 3 via an internal redox reaction, with the system retaining an 8‐electron superatomic configuration. The interstitial hydride in 1 and 2 contributes its 1s1 electron to the superatomic electron count and occupies a PdAg3 tetrahedron. The distributions of isomers corresponding to different dispositions of the outer capping Ag atoms are investigated by multinuclear VT NMR spectroscopy. The emissive state of 3 has a lifetime of 200 μs (λex=448; λem=842), while 1 and 2 are non‐emissive. The catalytic reduction of 4‐nitrophenol is demonstrated with 1–3 at room temperature. The first controlled modification of kernel and shell arrangements in Pd‐doped superatomic silver clusters containing interstitial hydrides is presented. The sequential addition of individual Ag atoms to an icosahedron core results in PdH@Ag19, PdH@Ag20, and Pd@Ag21, while maintaining a 12‐ligand stabilizing framework. Remarkable aqueous stability, proven by unsupported catalytic reduction of 4‐nitrophenol was demonstrated.
doi_str_mv 10.1002/chem.202300730
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The emissive state of 3 has a lifetime of 200 μs (λex=448; λem=842), while 1 and 2 are non‐emissive. The catalytic reduction of 4‐nitrophenol is demonstrated with 1–3 at room temperature. The first controlled modification of kernel and shell arrangements in Pd‐doped superatomic silver clusters containing interstitial hydrides is presented. The sequential addition of individual Ag atoms to an icosahedron core results in PdH@Ag19, PdH@Ag20, and Pd@Ag21, while maintaining a 12‐ligand stabilizing framework. Remarkable aqueous stability, proven by unsupported catalytic reduction of 4‐nitrophenol was demonstrated.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.202300730</identifier><identifier>PMID: 36897064</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>atomically precise nanoclusters ; Catalysis ; Chemical reduction ; Chemical Sciences ; Chemistry ; dithiophosphate ; Hydrides ; Isomers ; Magnetic resonance spectroscopy ; Material chemistry ; Nanoclusters ; Nitrophenol ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; or physical chemistry ; Palladium ; palladium hydrides ; Redox reactions ; Room temperature ; Silver ; superatoms ; Tetrahedra ; Theoretical and ; Trifluoroacetic acid</subject><ispartof>Chemistry : a European journal, 2023-06, Vol.29 (31), p.e202300730-n/a</ispartof><rights>2023 Wiley‐VCH GmbH</rights><rights>2023 Wiley-VCH GmbH.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4470-4ac3aec1ec3feb3f2512bf9beb90a3ee2011909733530ba05cd3734914c553cf3</citedby><cites>FETCH-LOGICAL-c4470-4ac3aec1ec3feb3f2512bf9beb90a3ee2011909733530ba05cd3734914c553cf3</cites><orcidid>0000-0003-0801-6499 ; 0000-0003-1285-1067 ; 0000-0001-5719-553X ; 0000-0003-4469-7922 ; 0000-0003-2826-465X ; 0000-0001-8697-8840</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36897064$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04061756$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ni, Yu‐Rong</creatorcontrib><creatorcontrib>Pillay, Michael N.</creatorcontrib><creatorcontrib>Chiu, Tzu‐Hao</creatorcontrib><creatorcontrib>Wu, Ying‐Yann</creatorcontrib><creatorcontrib>Kahlal, Samia</creatorcontrib><creatorcontrib>Saillard, Jean‐Yves</creatorcontrib><creatorcontrib>Liu, C. W.</creatorcontrib><title>Controlled Shell and Kernel Modifications of Atomically Precise Pd/Ag Superatomic Nanoclusters</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>The first 8‐electron Pd/Ag superatomic alloys with an interstitial hydride [PdHAg19(dtp)12] (dtp=S2P(OiPr)2−) 1 and [PdHAg20(dtp)12]+ 2 are reported. The targeted addition of a single Ag atom to 1 is achieved by the reaction of one equivalent of trifluoroacetic acid, resulting in the formation of 2 in 55 % yield. Further modification of the shell results in the formation of [PdAg21(dtp)12]+ 3 via an internal redox reaction, with the system retaining an 8‐electron superatomic configuration. The interstitial hydride in 1 and 2 contributes its 1s1 electron to the superatomic electron count and occupies a PdAg3 tetrahedron. The distributions of isomers corresponding to different dispositions of the outer capping Ag atoms are investigated by multinuclear VT NMR spectroscopy. 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W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controlled Shell and Kernel Modifications of Atomically Precise Pd/Ag Superatomic Nanoclusters</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2023-06-02</date><risdate>2023</risdate><volume>29</volume><issue>31</issue><spage>e202300730</spage><epage>n/a</epage><pages>e202300730-n/a</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>The first 8‐electron Pd/Ag superatomic alloys with an interstitial hydride [PdHAg19(dtp)12] (dtp=S2P(OiPr)2−) 1 and [PdHAg20(dtp)12]+ 2 are reported. The targeted addition of a single Ag atom to 1 is achieved by the reaction of one equivalent of trifluoroacetic acid, resulting in the formation of 2 in 55 % yield. Further modification of the shell results in the formation of [PdAg21(dtp)12]+ 3 via an internal redox reaction, with the system retaining an 8‐electron superatomic configuration. The interstitial hydride in 1 and 2 contributes its 1s1 electron to the superatomic electron count and occupies a PdAg3 tetrahedron. The distributions of isomers corresponding to different dispositions of the outer capping Ag atoms are investigated by multinuclear VT NMR spectroscopy. The emissive state of 3 has a lifetime of 200 μs (λex=448; λem=842), while 1 and 2 are non‐emissive. The catalytic reduction of 4‐nitrophenol is demonstrated with 1–3 at room temperature. The first controlled modification of kernel and shell arrangements in Pd‐doped superatomic silver clusters containing interstitial hydrides is presented. The sequential addition of individual Ag atoms to an icosahedron core results in PdH@Ag19, PdH@Ag20, and Pd@Ag21, while maintaining a 12‐ligand stabilizing framework. 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ispartof Chemistry : a European journal, 2023-06, Vol.29 (31), p.e202300730-n/a
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1521-3765
language eng
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subjects atomically precise nanoclusters
Catalysis
Chemical reduction
Chemical Sciences
Chemistry
dithiophosphate
Hydrides
Isomers
Magnetic resonance spectroscopy
Material chemistry
Nanoclusters
Nitrophenol
NMR
NMR spectroscopy
Nuclear magnetic resonance
or physical chemistry
Palladium
palladium hydrides
Redox reactions
Room temperature
Silver
superatoms
Tetrahedra
Theoretical and
Trifluoroacetic acid
title Controlled Shell and Kernel Modifications of Atomically Precise Pd/Ag Superatomic Nanoclusters
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