Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis
Pincer-type ligands are believed to be very robust scaffolds that can support multifarious functionalities as well as highly reactive metal motifs applied in organometallic chemistry, especially in the realm of catalysis. In this paper, we describe the redox and, therefore, noninnocent behavior of a...
Gespeichert in:
Veröffentlicht in: | Journal of the American Chemical Society 2008-03, Vol.130 (11), p.3676-3682 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3682 |
---|---|
container_issue | 11 |
container_start_page | 3676 |
container_title | Journal of the American Chemical Society |
container_volume | 130 |
creator | Adhikari, Debashis Mossin, Susanne Basuli, Falguni Huffman, John C Szilagyi, Robert K Meyer, Karsten Mindiola, Daniel J |
description | Pincer-type ligands are believed to be very robust scaffolds that can support multifarious functionalities as well as highly reactive metal motifs applied in organometallic chemistry, especially in the realm of catalysis. In this paper, we describe the redox and, therefore, noninnocent behavior of a PNP (PNP- = N[2-P(CHMe2)2-4-methylphenyl]2) pincer ancillary bound to nickel. A combination of structural, spectroscopic, and theoretical techniques suggests that this type of framework can house an electron hole when coordinated to Ni(II). |
doi_str_mv | 10.1021/ja7108486 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70388717</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70388717</sourcerecordid><originalsourceid>FETCH-LOGICAL-a417t-9cb98abd78b16e8cb9fd92a7297f04f2622783451c359948a844a2e85f24404f3</originalsourceid><addsrcrecordid>eNptkM1vEzEQxS0EomnhwD-AfAGpUhf8tWvvMYrKhxSJQgJXa-KdFQ6b9WJ7UfPf4ypRuXAaPc1Pb948Ql5x9o4zwd_vQXNmlGmekAWvBatqLpqnZMEYE5U2jbwglynti1TC8OfkghvJhDRqQdImx9nlOcJwQzcTuhxDcmHy7obC2NHtTwwRs3cw0Nthdr6D7MNIQ0-BfsMu3FdLl_0fpHd-dBir7XFCuhydHwaIR7qcpsFjR_1IV5BhOCafXpBnPQwJX57nFfn-4Xa7-lStv3z8vFquK1Bc56p1u9bArtNmxxs0RfVdK0CLVvdM9aIRQhupau5k3bbKgFEKBJq6F0oVQF6RtyffKYbfM6ZsDz45LMFGDHOymkljNNcFvD6BrjyfIvZ2iv5Q4lvO7EPD9rHhwr4-m867A3b_yHOlBahOgE8Z7x_3EH_ZRktd2-3dxkrz4-umXnP7YPjmxINLdh_mOJZO_nP4L3kDkLI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70388717</pqid></control><display><type>article</type><title>Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Adhikari, Debashis ; Mossin, Susanne ; Basuli, Falguni ; Huffman, John C ; Szilagyi, Robert K ; Meyer, Karsten ; Mindiola, Daniel J</creator><creatorcontrib>Adhikari, Debashis ; Mossin, Susanne ; Basuli, Falguni ; Huffman, John C ; Szilagyi, Robert K ; Meyer, Karsten ; Mindiola, Daniel J</creatorcontrib><description>Pincer-type ligands are believed to be very robust scaffolds that can support multifarious functionalities as well as highly reactive metal motifs applied in organometallic chemistry, especially in the realm of catalysis. In this paper, we describe the redox and, therefore, noninnocent behavior of a PNP (PNP- = N[2-P(CHMe2)2-4-methylphenyl]2) pincer ancillary bound to nickel. A combination of structural, spectroscopic, and theoretical techniques suggests that this type of framework can house an electron hole when coordinated to Ni(II).</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja7108486</identifier><identifier>PMID: 18302384</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Catalysis ; Cations - chemical synthesis ; Cations - chemistry ; Electron Spin Resonance Spectroscopy - methods ; Free Radicals - chemical synthesis ; Free Radicals - chemistry ; Ligands ; Models, Molecular ; Nickel - chemistry ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Oxidation-Reduction ; Quantum Theory ; Spectrometry, X-Ray Emission - methods ; Spectrophotometry, Ultraviolet - methods ; X-Ray Diffraction</subject><ispartof>Journal of the American Chemical Society, 2008-03, Vol.130 (11), p.3676-3682</ispartof><rights>Copyright © 2008 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a417t-9cb98abd78b16e8cb9fd92a7297f04f2622783451c359948a844a2e85f24404f3</citedby><cites>FETCH-LOGICAL-a417t-9cb98abd78b16e8cb9fd92a7297f04f2622783451c359948a844a2e85f24404f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja7108486$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja7108486$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18302384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adhikari, Debashis</creatorcontrib><creatorcontrib>Mossin, Susanne</creatorcontrib><creatorcontrib>Basuli, Falguni</creatorcontrib><creatorcontrib>Huffman, John C</creatorcontrib><creatorcontrib>Szilagyi, Robert K</creatorcontrib><creatorcontrib>Meyer, Karsten</creatorcontrib><creatorcontrib>Mindiola, Daniel J</creatorcontrib><title>Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Pincer-type ligands are believed to be very robust scaffolds that can support multifarious functionalities as well as highly reactive metal motifs applied in organometallic chemistry, especially in the realm of catalysis. In this paper, we describe the redox and, therefore, noninnocent behavior of a PNP (PNP- = N[2-P(CHMe2)2-4-methylphenyl]2) pincer ancillary bound to nickel. A combination of structural, spectroscopic, and theoretical techniques suggests that this type of framework can house an electron hole when coordinated to Ni(II).</description><subject>Catalysis</subject><subject>Cations - chemical synthesis</subject><subject>Cations - chemistry</subject><subject>Electron Spin Resonance Spectroscopy - methods</subject><subject>Free Radicals - chemical synthesis</subject><subject>Free Radicals - chemistry</subject><subject>Ligands</subject><subject>Models, Molecular</subject><subject>Nickel - chemistry</subject><subject>Organometallic Compounds - chemical synthesis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Oxidation-Reduction</subject><subject>Quantum Theory</subject><subject>Spectrometry, X-Ray Emission - methods</subject><subject>Spectrophotometry, Ultraviolet - methods</subject><subject>X-Ray Diffraction</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkM1vEzEQxS0EomnhwD-AfAGpUhf8tWvvMYrKhxSJQgJXa-KdFQ6b9WJ7UfPf4ypRuXAaPc1Pb948Ql5x9o4zwd_vQXNmlGmekAWvBatqLpqnZMEYE5U2jbwglynti1TC8OfkghvJhDRqQdImx9nlOcJwQzcTuhxDcmHy7obC2NHtTwwRs3cw0Nthdr6D7MNIQ0-BfsMu3FdLl_0fpHd-dBir7XFCuhydHwaIR7qcpsFjR_1IV5BhOCafXpBnPQwJX57nFfn-4Xa7-lStv3z8vFquK1Bc56p1u9bArtNmxxs0RfVdK0CLVvdM9aIRQhupau5k3bbKgFEKBJq6F0oVQF6RtyffKYbfM6ZsDz45LMFGDHOymkljNNcFvD6BrjyfIvZ2iv5Q4lvO7EPD9rHhwr4-m867A3b_yHOlBahOgE8Z7x_3EH_ZRktd2-3dxkrz4-umXnP7YPjmxINLdh_mOJZO_nP4L3kDkLI</recordid><startdate>20080319</startdate><enddate>20080319</enddate><creator>Adhikari, Debashis</creator><creator>Mossin, Susanne</creator><creator>Basuli, Falguni</creator><creator>Huffman, John C</creator><creator>Szilagyi, Robert K</creator><creator>Meyer, Karsten</creator><creator>Mindiola, Daniel J</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080319</creationdate><title>Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis</title><author>Adhikari, Debashis ; Mossin, Susanne ; Basuli, Falguni ; Huffman, John C ; Szilagyi, Robert K ; Meyer, Karsten ; Mindiola, Daniel J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a417t-9cb98abd78b16e8cb9fd92a7297f04f2622783451c359948a844a2e85f24404f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Catalysis</topic><topic>Cations - chemical synthesis</topic><topic>Cations - chemistry</topic><topic>Electron Spin Resonance Spectroscopy - methods</topic><topic>Free Radicals - chemical synthesis</topic><topic>Free Radicals - chemistry</topic><topic>Ligands</topic><topic>Models, Molecular</topic><topic>Nickel - chemistry</topic><topic>Organometallic Compounds - chemical synthesis</topic><topic>Organometallic Compounds - chemistry</topic><topic>Oxidation-Reduction</topic><topic>Quantum Theory</topic><topic>Spectrometry, X-Ray Emission - methods</topic><topic>Spectrophotometry, Ultraviolet - methods</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adhikari, Debashis</creatorcontrib><creatorcontrib>Mossin, Susanne</creatorcontrib><creatorcontrib>Basuli, Falguni</creatorcontrib><creatorcontrib>Huffman, John C</creatorcontrib><creatorcontrib>Szilagyi, Robert K</creatorcontrib><creatorcontrib>Meyer, Karsten</creatorcontrib><creatorcontrib>Mindiola, Daniel J</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adhikari, Debashis</au><au>Mossin, Susanne</au><au>Basuli, Falguni</au><au>Huffman, John C</au><au>Szilagyi, Robert K</au><au>Meyer, Karsten</au><au>Mindiola, Daniel J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2008-03-19</date><risdate>2008</risdate><volume>130</volume><issue>11</issue><spage>3676</spage><epage>3682</epage><pages>3676-3682</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Pincer-type ligands are believed to be very robust scaffolds that can support multifarious functionalities as well as highly reactive metal motifs applied in organometallic chemistry, especially in the realm of catalysis. In this paper, we describe the redox and, therefore, noninnocent behavior of a PNP (PNP- = N[2-P(CHMe2)2-4-methylphenyl]2) pincer ancillary bound to nickel. A combination of structural, spectroscopic, and theoretical techniques suggests that this type of framework can house an electron hole when coordinated to Ni(II).</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>18302384</pmid><doi>10.1021/ja7108486</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-7863 |
ispartof | Journal of the American Chemical Society, 2008-03, Vol.130 (11), p.3676-3682 |
issn | 0002-7863 1520-5126 |
language | eng |
recordid | cdi_proquest_miscellaneous_70388717 |
source | MEDLINE; American Chemical Society Journals |
subjects | Catalysis Cations - chemical synthesis Cations - chemistry Electron Spin Resonance Spectroscopy - methods Free Radicals - chemical synthesis Free Radicals - chemistry Ligands Models, Molecular Nickel - chemistry Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Oxidation-Reduction Quantum Theory Spectrometry, X-Ray Emission - methods Spectrophotometry, Ultraviolet - methods X-Ray Diffraction |
title | Structural, Spectroscopic, and Theoretical Elucidation of a Redox-Active Pincer-Type Ancillary Applied in Catalysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T23%3A27%3A53IST&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=Structural,%20Spectroscopic,%20and%20Theoretical%20Elucidation%20of%20a%20Redox-Active%20Pincer-Type%20Ancillary%20Applied%20in%20Catalysis&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Adhikari,%20Debashis&rft.date=2008-03-19&rft.volume=130&rft.issue=11&rft.spage=3676&rft.epage=3682&rft.pages=3676-3682&rft.issn=0002-7863&rft.eissn=1520-5126&rft_id=info:doi/10.1021/ja7108486&rft_dat=%3Cproquest_cross%3E70388717%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=70388717&rft_id=info:pmid/18302384&rfr_iscdi=true |