Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction

Recent advances in organic surface sensitization of metal oxide nanomaterials focused on two-step approaches with the first step providing a convenient functionalized chemical “hook”, such as an alkyne functionality connected to a carboxylic group in prop-2-ynoic acid. The second step then took adva...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Langmuir 2020-12, Vol.36 (48), p.14539-14545
Hauptverfasser: He, Chuan, Cai, Xuefen, Wei, Su-Huai, Janotti, Anderson, Teplyakov, Andrew V
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 14545
container_issue 48
container_start_page 14539
container_title Langmuir
container_volume 36
creator He, Chuan
Cai, Xuefen
Wei, Su-Huai
Janotti, Anderson
Teplyakov, Andrew V
description Recent advances in organic surface sensitization of metal oxide nanomaterials focused on two-step approaches with the first step providing a convenient functionalized chemical “hook”, such as an alkyne functionality connected to a carboxylic group in prop-2-ynoic acid. The second step then took advantage of copper-catalyzed click chemistry to deliver the desired structure (such as benzyl or perylene) attached to an azide to react with the surface-bound alkyne. The use of this approach on CuO not only resulted in a successful morphology preserving chemical modification but also has demonstrated that surface Cu­(I) can be obtained during the process and promote a surface-catalyzed click reaction without additional copper catalyst. Here, it is demonstrated that this surface-catalyzed chemistry can be performed on a surface of the CuO nanomaterial without a solvent, as a “dry click” reaction, as confirmed with spectroscopic and microscopic investigations with X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, solid-state nuclear magnetic resonance, and scanning electron microscopy. Computational studies provided instructive information on the interaction between the surface prop-2-yonate and azide functional group to better understand the mechanism of this surface-catalyzed click reaction.
doi_str_mv 10.1021/acs.langmuir.0c02262
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2464607227</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2464607227</sourcerecordid><originalsourceid>FETCH-LOGICAL-a391t-56a8e806d6c6bbc045390a0af31535f2891623483e10bd930828b8e87a11a5003</originalsourceid><addsrcrecordid>eNp9kD1PwzAURS0EEqXwDxg8sqQ8f8RJRhQBRaqoRGG2XlwHuaRxsZOi9teTqmVlusO750n3EHLLYMKAs3s0cdJg-7nuXZiAAc4VPyMjlnJI0pxn52QEmRRJJpW4JFcxrgCgELIYkfnCNnVSYofNbm-XdGHb6Dq3x875lvqalv2cvmLrf1ywkW4dUqQL32xt2yV1sJaWjTNf9M2iOSDX5KLGJtqbU47Jx9PjezlNZvPnl_JhlqAoWJekCnObg1oqo6rKgExFAQhYC5aKtOZ5wRQXMheWQbUsBOQ8rwYiQ8YwBRBjcnf8uwn-u7ex02sXjW0GDdb3UXOppIKM82yoymPVBB9jsLXeBLfGsNMM9MGfHvzpP3_65G_A4Igdrivfh3bY8z_yC7Pqdkc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2464607227</pqid></control><display><type>article</type><title>Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction</title><source>American Chemical Society (ACS) Journals</source><creator>He, Chuan ; Cai, Xuefen ; Wei, Su-Huai ; Janotti, Anderson ; Teplyakov, Andrew V</creator><creatorcontrib>He, Chuan ; Cai, Xuefen ; Wei, Su-Huai ; Janotti, Anderson ; Teplyakov, Andrew V</creatorcontrib><description>Recent advances in organic surface sensitization of metal oxide nanomaterials focused on two-step approaches with the first step providing a convenient functionalized chemical “hook”, such as an alkyne functionality connected to a carboxylic group in prop-2-ynoic acid. The second step then took advantage of copper-catalyzed click chemistry to deliver the desired structure (such as benzyl or perylene) attached to an azide to react with the surface-bound alkyne. The use of this approach on CuO not only resulted in a successful morphology preserving chemical modification but also has demonstrated that surface Cu­(I) can be obtained during the process and promote a surface-catalyzed click reaction without additional copper catalyst. Here, it is demonstrated that this surface-catalyzed chemistry can be performed on a surface of the CuO nanomaterial without a solvent, as a “dry click” reaction, as confirmed with spectroscopic and microscopic investigations with X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, solid-state nuclear magnetic resonance, and scanning electron microscopy. Computational studies provided instructive information on the interaction between the surface prop-2-yonate and azide functional group to better understand the mechanism of this surface-catalyzed click reaction.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/acs.langmuir.0c02262</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Langmuir, 2020-12, Vol.36 (48), p.14539-14545</ispartof><rights>2020 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a391t-56a8e806d6c6bbc045390a0af31535f2891623483e10bd930828b8e87a11a5003</citedby><cites>FETCH-LOGICAL-a391t-56a8e806d6c6bbc045390a0af31535f2891623483e10bd930828b8e87a11a5003</cites><orcidid>0000-0002-0358-2101 ; 0000-0003-1563-4738 ; 0000-0002-6646-3310</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.langmuir.0c02262$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.langmuir.0c02262$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>He, Chuan</creatorcontrib><creatorcontrib>Cai, Xuefen</creatorcontrib><creatorcontrib>Wei, Su-Huai</creatorcontrib><creatorcontrib>Janotti, Anderson</creatorcontrib><creatorcontrib>Teplyakov, Andrew V</creatorcontrib><title>Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Recent advances in organic surface sensitization of metal oxide nanomaterials focused on two-step approaches with the first step providing a convenient functionalized chemical “hook”, such as an alkyne functionality connected to a carboxylic group in prop-2-ynoic acid. The second step then took advantage of copper-catalyzed click chemistry to deliver the desired structure (such as benzyl or perylene) attached to an azide to react with the surface-bound alkyne. The use of this approach on CuO not only resulted in a successful morphology preserving chemical modification but also has demonstrated that surface Cu­(I) can be obtained during the process and promote a surface-catalyzed click reaction without additional copper catalyst. Here, it is demonstrated that this surface-catalyzed chemistry can be performed on a surface of the CuO nanomaterial without a solvent, as a “dry click” reaction, as confirmed with spectroscopic and microscopic investigations with X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, solid-state nuclear magnetic resonance, and scanning electron microscopy. Computational studies provided instructive information on the interaction between the surface prop-2-yonate and azide functional group to better understand the mechanism of this surface-catalyzed click reaction.</description><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kD1PwzAURS0EEqXwDxg8sqQ8f8RJRhQBRaqoRGG2XlwHuaRxsZOi9teTqmVlusO750n3EHLLYMKAs3s0cdJg-7nuXZiAAc4VPyMjlnJI0pxn52QEmRRJJpW4JFcxrgCgELIYkfnCNnVSYofNbm-XdGHb6Dq3x875lvqalv2cvmLrf1ywkW4dUqQL32xt2yV1sJaWjTNf9M2iOSDX5KLGJtqbU47Jx9PjezlNZvPnl_JhlqAoWJekCnObg1oqo6rKgExFAQhYC5aKtOZ5wRQXMheWQbUsBOQ8rwYiQ8YwBRBjcnf8uwn-u7ex02sXjW0GDdb3UXOppIKM82yoymPVBB9jsLXeBLfGsNMM9MGfHvzpP3_65G_A4Igdrivfh3bY8z_yC7Pqdkc</recordid><startdate>20201208</startdate><enddate>20201208</enddate><creator>He, Chuan</creator><creator>Cai, Xuefen</creator><creator>Wei, Su-Huai</creator><creator>Janotti, Anderson</creator><creator>Teplyakov, Andrew V</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0358-2101</orcidid><orcidid>https://orcid.org/0000-0003-1563-4738</orcidid><orcidid>https://orcid.org/0000-0002-6646-3310</orcidid></search><sort><creationdate>20201208</creationdate><title>Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction</title><author>He, Chuan ; Cai, Xuefen ; Wei, Su-Huai ; Janotti, Anderson ; Teplyakov, Andrew V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a391t-56a8e806d6c6bbc045390a0af31535f2891623483e10bd930828b8e87a11a5003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Chuan</creatorcontrib><creatorcontrib>Cai, Xuefen</creatorcontrib><creatorcontrib>Wei, Su-Huai</creatorcontrib><creatorcontrib>Janotti, Anderson</creatorcontrib><creatorcontrib>Teplyakov, Andrew V</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Chuan</au><au>Cai, Xuefen</au><au>Wei, Su-Huai</au><au>Janotti, Anderson</au><au>Teplyakov, Andrew V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2020-12-08</date><risdate>2020</risdate><volume>36</volume><issue>48</issue><spage>14539</spage><epage>14545</epage><pages>14539-14545</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><abstract>Recent advances in organic surface sensitization of metal oxide nanomaterials focused on two-step approaches with the first step providing a convenient functionalized chemical “hook”, such as an alkyne functionality connected to a carboxylic group in prop-2-ynoic acid. The second step then took advantage of copper-catalyzed click chemistry to deliver the desired structure (such as benzyl or perylene) attached to an azide to react with the surface-bound alkyne. The use of this approach on CuO not only resulted in a successful morphology preserving chemical modification but also has demonstrated that surface Cu­(I) can be obtained during the process and promote a surface-catalyzed click reaction without additional copper catalyst. Here, it is demonstrated that this surface-catalyzed chemistry can be performed on a surface of the CuO nanomaterial without a solvent, as a “dry click” reaction, as confirmed with spectroscopic and microscopic investigations with X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, solid-state nuclear magnetic resonance, and scanning electron microscopy. Computational studies provided instructive information on the interaction between the surface prop-2-yonate and azide functional group to better understand the mechanism of this surface-catalyzed click reaction.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.langmuir.0c02262</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0358-2101</orcidid><orcidid>https://orcid.org/0000-0003-1563-4738</orcidid><orcidid>https://orcid.org/0000-0002-6646-3310</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0743-7463
ispartof Langmuir, 2020-12, Vol.36 (48), p.14539-14545
issn 0743-7463
1520-5827
language eng
recordid cdi_proquest_miscellaneous_2464607227
source American Chemical Society (ACS) Journals
title Self-Catalyzed Sensitization of CuO Nanowires via a Solvent-free Click Reaction
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T17%3A15%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Self-Catalyzed%20Sensitization%20of%20CuO%20Nanowires%20via%20a%20Solvent-free%20Click%20Reaction&rft.jtitle=Langmuir&rft.au=He,%20Chuan&rft.date=2020-12-08&rft.volume=36&rft.issue=48&rft.spage=14539&rft.epage=14545&rft.pages=14539-14545&rft.issn=0743-7463&rft.eissn=1520-5827&rft_id=info:doi/10.1021/acs.langmuir.0c02262&rft_dat=%3Cproquest_cross%3E2464607227%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2464607227&rft_id=info:pmid/&rfr_iscdi=true