Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands
Incorporating radical ligands into metal complexes is one of the emerging trends in the design of single-molecule magnets (SMMs). While significant effort has been expended to generate multinuclear transition metal-based SMMs with bridging radical ligands, less attention has been paid to mononuclear...
Gespeichert in:
Veröffentlicht in: | Inorganic chemistry 2021-05, Vol.60 (9), p.6480-6491 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 6491 |
---|---|
container_issue | 9 |
container_start_page | 6480 |
container_title | Inorganic chemistry |
container_volume | 60 |
creator | Wang, Peng Saber, Mohamed R VanNatta, Peter E Yap, Glenn P. A Popescu, Codrina V Scarborough, Christopher C Kieber-Emmons, Matthew T Dunbar, Kim R Riordan, Charles G |
description | Incorporating radical ligands into metal complexes is one of the emerging trends in the design of single-molecule magnets (SMMs). While significant effort has been expended to generate multinuclear transition metal-based SMMs with bridging radical ligands, less attention has been paid to mononuclear transition metal–radical SMMs. Herein, we describe the first α-diiminato radical-containing mononuclear transition metal SMM, namely, [κ2-PhTt tBu]Fe(AdNCHCHNAd) (1), and its analogue [κ2-PhTt tBu]Fe(CyNCHCHNCy) (2) (PhTt tBu = phenyltris(tert-butylthiomethyl)borate, Ad = adamantyl, and Cy = cyclohexyl). 1 and 2 feature nearly identical geometric and electronic structures, as shown by X-ray crystallography and electronic absorption spectroscopy. A more detailed description of the electronic structure of 1 was obtained through EPR and Mössbauer spectroscopies, SQUID magnetometry, and DFT, TD-DFT, and CAS calculations. 1 and 2 are best described as high-spin iron(II) complexes with antiferromagnetically coupled α-diiminato radical ligands. A strong magnetic exchange coupling between the iron(II) ion and the ligand radical was confirmed in 1, with an estimated coupling constant J < −250 cm–1 (J = −657 cm–1, DFT). Calibrated CAS calculations revealed that the ground-state Fe(II)−α-diiminato radical configuration has significant ionic contributions, which are weighted specifically toward the Fe(I)-neutral α-diimine species. Experimental data and theoretical calculations also suggest that 1 possesses an easy-axis anisotropy, with an axial zero-field splitting parameter D in the range from −4 to–1 cm–1. Finally, dynamic magnetic studies show that 1 exhibits slow magnetic relaxation behavior with an energy barrier close to the theoretical maximum, 2|D|. These results demonstrate that incorporating strongly coupled α-diiminato radicals into mononuclear transition metal complexes can be an effective strategy to prepare SMMs. |
doi_str_mv | 10.1021/acs.inorgchem.1c00214 |
format | Article |
fullrecord | <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_1853683</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2511900904</sourcerecordid><originalsourceid>FETCH-LOGICAL-a425t-f5d53a115aac786fcb5fb304bb3e9f77f13a38305fd44fcc99204b20904b908d3</originalsourceid><addsrcrecordid>eNqFkcFu1DAQhi0EotvCI4AsTu0hix3H2fhYlgKVtkKiReJmOc544yqxF9upyq2vgLjwGrwID9EnwcsuvXLxyDPf_480P0IvKJlTUtLXSse5dT6sdQ_jnGqSm9UjNKO8JAWn5MtjNMs9UtC6FgfoMMZrQohgVf0UHTDWVIQ2YoZ-XvgB9DSogJXr8Fn-pOCd1fgyhUmnKUD8O7m0bj1AsccBX6i1g4TfQK9urA_YG3wVbDxOvfWQeggn93c_zrMVXvpxM8Bt9ll6l5R12Ql_gs7fFqc62RvAv3_d331_a-1oHeCVXed98Rl6YtQQ4fm-HqHP786ulh-K1cf358vTVaGqkqfC8I4zRSlXSi-a2uiWm5aRqm0ZCLNYGMoUaxjhpqsqo7UQZR6WRORXkKZjR-jVztfHZGXUNoHutXcuH0LShrO6YRk63kGb4L9OEJMcbdQwDMqBn6IsOaWCbE0zyneoDj7GAEZugh1V-CYpkdvkZE5OPiQn98ll3cv9iqkdoXtQ_YsqA3QHbPXXfgoun-U_pn8AP3it_w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2511900904</pqid></control><display><type>article</type><title>Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands</title><source>American Chemical Society Journals</source><creator>Wang, Peng ; Saber, Mohamed R ; VanNatta, Peter E ; Yap, Glenn P. A ; Popescu, Codrina V ; Scarborough, Christopher C ; Kieber-Emmons, Matthew T ; Dunbar, Kim R ; Riordan, Charles G</creator><creatorcontrib>Wang, Peng ; Saber, Mohamed R ; VanNatta, Peter E ; Yap, Glenn P. A ; Popescu, Codrina V ; Scarborough, Christopher C ; Kieber-Emmons, Matthew T ; Dunbar, Kim R ; Riordan, Charles G ; Univ. of Utah, Salt Lake City, UT (United States)</creatorcontrib><description>Incorporating radical ligands into metal complexes is one of the emerging trends in the design of single-molecule magnets (SMMs). While significant effort has been expended to generate multinuclear transition metal-based SMMs with bridging radical ligands, less attention has been paid to mononuclear transition metal–radical SMMs. Herein, we describe the first α-diiminato radical-containing mononuclear transition metal SMM, namely, [κ2-PhTt tBu]Fe(AdNCHCHNAd) (1), and its analogue [κ2-PhTt tBu]Fe(CyNCHCHNCy) (2) (PhTt tBu = phenyltris(tert-butylthiomethyl)borate, Ad = adamantyl, and Cy = cyclohexyl). 1 and 2 feature nearly identical geometric and electronic structures, as shown by X-ray crystallography and electronic absorption spectroscopy. A more detailed description of the electronic structure of 1 was obtained through EPR and Mössbauer spectroscopies, SQUID magnetometry, and DFT, TD-DFT, and CAS calculations. 1 and 2 are best described as high-spin iron(II) complexes with antiferromagnetically coupled α-diiminato radical ligands. A strong magnetic exchange coupling between the iron(II) ion and the ligand radical was confirmed in 1, with an estimated coupling constant J < −250 cm–1 (J = −657 cm–1, DFT). Calibrated CAS calculations revealed that the ground-state Fe(II)−α-diiminato radical configuration has significant ionic contributions, which are weighted specifically toward the Fe(I)-neutral α-diimine species. Experimental data and theoretical calculations also suggest that 1 possesses an easy-axis anisotropy, with an axial zero-field splitting parameter D in the range from −4 to–1 cm–1. Finally, dynamic magnetic studies show that 1 exhibits slow magnetic relaxation behavior with an energy barrier close to the theoretical maximum, 2|D|. These results demonstrate that incorporating strongly coupled α-diiminato radicals into mononuclear transition metal complexes can be an effective strategy to prepare SMMs.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.1c00214</identifier><identifier>PMID: 33840189</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Chemistry</subject><ispartof>Inorganic chemistry, 2021-05, Vol.60 (9), p.6480-6491</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a425t-f5d53a115aac786fcb5fb304bb3e9f77f13a38305fd44fcc99204b20904b908d3</citedby><cites>FETCH-LOGICAL-a425t-f5d53a115aac786fcb5fb304bb3e9f77f13a38305fd44fcc99204b20904b908d3</cites><orcidid>0000-0003-1360-579X ; 0000-0002-6357-5579 ; 0000-0003-2369-3383 ; 0000-0001-5728-7805 ; 0000-0002-8572-4571 ; 0000-0002-7991-2541 ; 0000000323693383 ; 0000000263575579 ; 0000000285724571 ; 0000000279912541 ; 0000000157287805 ; 000000031360579X</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.inorgchem.1c00214$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.inorgchem.1c00214$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33840189$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1853683$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Peng</creatorcontrib><creatorcontrib>Saber, Mohamed R</creatorcontrib><creatorcontrib>VanNatta, Peter E</creatorcontrib><creatorcontrib>Yap, Glenn P. A</creatorcontrib><creatorcontrib>Popescu, Codrina V</creatorcontrib><creatorcontrib>Scarborough, Christopher C</creatorcontrib><creatorcontrib>Kieber-Emmons, Matthew T</creatorcontrib><creatorcontrib>Dunbar, Kim R</creatorcontrib><creatorcontrib>Riordan, Charles G</creatorcontrib><creatorcontrib>Univ. of Utah, Salt Lake City, UT (United States)</creatorcontrib><title>Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>Incorporating radical ligands into metal complexes is one of the emerging trends in the design of single-molecule magnets (SMMs). While significant effort has been expended to generate multinuclear transition metal-based SMMs with bridging radical ligands, less attention has been paid to mononuclear transition metal–radical SMMs. Herein, we describe the first α-diiminato radical-containing mononuclear transition metal SMM, namely, [κ2-PhTt tBu]Fe(AdNCHCHNAd) (1), and its analogue [κ2-PhTt tBu]Fe(CyNCHCHNCy) (2) (PhTt tBu = phenyltris(tert-butylthiomethyl)borate, Ad = adamantyl, and Cy = cyclohexyl). 1 and 2 feature nearly identical geometric and electronic structures, as shown by X-ray crystallography and electronic absorption spectroscopy. A more detailed description of the electronic structure of 1 was obtained through EPR and Mössbauer spectroscopies, SQUID magnetometry, and DFT, TD-DFT, and CAS calculations. 1 and 2 are best described as high-spin iron(II) complexes with antiferromagnetically coupled α-diiminato radical ligands. A strong magnetic exchange coupling between the iron(II) ion and the ligand radical was confirmed in 1, with an estimated coupling constant J < −250 cm–1 (J = −657 cm–1, DFT). Calibrated CAS calculations revealed that the ground-state Fe(II)−α-diiminato radical configuration has significant ionic contributions, which are weighted specifically toward the Fe(I)-neutral α-diimine species. Experimental data and theoretical calculations also suggest that 1 possesses an easy-axis anisotropy, with an axial zero-field splitting parameter D in the range from −4 to–1 cm–1. Finally, dynamic magnetic studies show that 1 exhibits slow magnetic relaxation behavior with an energy barrier close to the theoretical maximum, 2|D|. These results demonstrate that incorporating strongly coupled α-diiminato radicals into mononuclear transition metal complexes can be an effective strategy to prepare SMMs.</description><subject>Chemistry</subject><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EotvCI4AsTu0hix3H2fhYlgKVtkKiReJmOc544yqxF9upyq2vgLjwGrwID9EnwcsuvXLxyDPf_480P0IvKJlTUtLXSse5dT6sdQ_jnGqSm9UjNKO8JAWn5MtjNMs9UtC6FgfoMMZrQohgVf0UHTDWVIQ2YoZ-XvgB9DSogJXr8Fn-pOCd1fgyhUmnKUD8O7m0bj1AsccBX6i1g4TfQK9urA_YG3wVbDxOvfWQeggn93c_zrMVXvpxM8Bt9ll6l5R12Ql_gs7fFqc62RvAv3_d331_a-1oHeCVXed98Rl6YtQQ4fm-HqHP786ulh-K1cf358vTVaGqkqfC8I4zRSlXSi-a2uiWm5aRqm0ZCLNYGMoUaxjhpqsqo7UQZR6WRORXkKZjR-jVztfHZGXUNoHutXcuH0LShrO6YRk63kGb4L9OEJMcbdQwDMqBn6IsOaWCbE0zyneoDj7GAEZugh1V-CYpkdvkZE5OPiQn98ll3cv9iqkdoXtQ_YsqA3QHbPXXfgoun-U_pn8AP3it_w</recordid><startdate>20210503</startdate><enddate>20210503</enddate><creator>Wang, Peng</creator><creator>Saber, Mohamed R</creator><creator>VanNatta, Peter E</creator><creator>Yap, Glenn P. A</creator><creator>Popescu, Codrina V</creator><creator>Scarborough, Christopher C</creator><creator>Kieber-Emmons, Matthew T</creator><creator>Dunbar, Kim R</creator><creator>Riordan, Charles G</creator><general>American Chemical Society</general><general>American Chemical Society (ACS)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-1360-579X</orcidid><orcidid>https://orcid.org/0000-0002-6357-5579</orcidid><orcidid>https://orcid.org/0000-0003-2369-3383</orcidid><orcidid>https://orcid.org/0000-0001-5728-7805</orcidid><orcidid>https://orcid.org/0000-0002-8572-4571</orcidid><orcidid>https://orcid.org/0000-0002-7991-2541</orcidid><orcidid>https://orcid.org/0000000323693383</orcidid><orcidid>https://orcid.org/0000000263575579</orcidid><orcidid>https://orcid.org/0000000285724571</orcidid><orcidid>https://orcid.org/0000000279912541</orcidid><orcidid>https://orcid.org/0000000157287805</orcidid><orcidid>https://orcid.org/000000031360579X</orcidid></search><sort><creationdate>20210503</creationdate><title>Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands</title><author>Wang, Peng ; Saber, Mohamed R ; VanNatta, Peter E ; Yap, Glenn P. A ; Popescu, Codrina V ; Scarborough, Christopher C ; Kieber-Emmons, Matthew T ; Dunbar, Kim R ; Riordan, Charles G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a425t-f5d53a115aac786fcb5fb304bb3e9f77f13a38305fd44fcc99204b20904b908d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Peng</creatorcontrib><creatorcontrib>Saber, Mohamed R</creatorcontrib><creatorcontrib>VanNatta, Peter E</creatorcontrib><creatorcontrib>Yap, Glenn P. A</creatorcontrib><creatorcontrib>Popescu, Codrina V</creatorcontrib><creatorcontrib>Scarborough, Christopher C</creatorcontrib><creatorcontrib>Kieber-Emmons, Matthew T</creatorcontrib><creatorcontrib>Dunbar, Kim R</creatorcontrib><creatorcontrib>Riordan, Charles G</creatorcontrib><creatorcontrib>Univ. of Utah, Salt Lake City, UT (United States)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Peng</au><au>Saber, Mohamed R</au><au>VanNatta, Peter E</au><au>Yap, Glenn P. A</au><au>Popescu, Codrina V</au><au>Scarborough, Christopher C</au><au>Kieber-Emmons, Matthew T</au><au>Dunbar, Kim R</au><au>Riordan, Charles G</au><aucorp>Univ. of Utah, Salt Lake City, UT (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2021-05-03</date><risdate>2021</risdate><volume>60</volume><issue>9</issue><spage>6480</spage><epage>6491</epage><pages>6480-6491</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>Incorporating radical ligands into metal complexes is one of the emerging trends in the design of single-molecule magnets (SMMs). While significant effort has been expended to generate multinuclear transition metal-based SMMs with bridging radical ligands, less attention has been paid to mononuclear transition metal–radical SMMs. Herein, we describe the first α-diiminato radical-containing mononuclear transition metal SMM, namely, [κ2-PhTt tBu]Fe(AdNCHCHNAd) (1), and its analogue [κ2-PhTt tBu]Fe(CyNCHCHNCy) (2) (PhTt tBu = phenyltris(tert-butylthiomethyl)borate, Ad = adamantyl, and Cy = cyclohexyl). 1 and 2 feature nearly identical geometric and electronic structures, as shown by X-ray crystallography and electronic absorption spectroscopy. A more detailed description of the electronic structure of 1 was obtained through EPR and Mössbauer spectroscopies, SQUID magnetometry, and DFT, TD-DFT, and CAS calculations. 1 and 2 are best described as high-spin iron(II) complexes with antiferromagnetically coupled α-diiminato radical ligands. A strong magnetic exchange coupling between the iron(II) ion and the ligand radical was confirmed in 1, with an estimated coupling constant J < −250 cm–1 (J = −657 cm–1, DFT). Calibrated CAS calculations revealed that the ground-state Fe(II)−α-diiminato radical configuration has significant ionic contributions, which are weighted specifically toward the Fe(I)-neutral α-diimine species. Experimental data and theoretical calculations also suggest that 1 possesses an easy-axis anisotropy, with an axial zero-field splitting parameter D in the range from −4 to–1 cm–1. Finally, dynamic magnetic studies show that 1 exhibits slow magnetic relaxation behavior with an energy barrier close to the theoretical maximum, 2|D|. These results demonstrate that incorporating strongly coupled α-diiminato radicals into mononuclear transition metal complexes can be an effective strategy to prepare SMMs.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33840189</pmid><doi>10.1021/acs.inorgchem.1c00214</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-1360-579X</orcidid><orcidid>https://orcid.org/0000-0002-6357-5579</orcidid><orcidid>https://orcid.org/0000-0003-2369-3383</orcidid><orcidid>https://orcid.org/0000-0001-5728-7805</orcidid><orcidid>https://orcid.org/0000-0002-8572-4571</orcidid><orcidid>https://orcid.org/0000-0002-7991-2541</orcidid><orcidid>https://orcid.org/0000000323693383</orcidid><orcidid>https://orcid.org/0000000263575579</orcidid><orcidid>https://orcid.org/0000000285724571</orcidid><orcidid>https://orcid.org/0000000279912541</orcidid><orcidid>https://orcid.org/0000000157287805</orcidid><orcidid>https://orcid.org/000000031360579X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0020-1669 |
ispartof | Inorganic chemistry, 2021-05, Vol.60 (9), p.6480-6491 |
issn | 0020-1669 1520-510X |
language | eng |
recordid | cdi_osti_scitechconnect_1853683 |
source | American Chemical Society Journals |
subjects | Chemistry |
title | Molecular and Electronic Structures and Single-Molecule Magnet Behavior of Tris(thioether)–Iron Complexes Containing Redox-Active α‑Diimine Ligands |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T16%3A00%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20and%20Electronic%20Structures%20and%20Single-Molecule%20Magnet%20Behavior%20of%20Tris(thioether)%E2%80%93Iron%20Complexes%20Containing%20Redox-Active%20%CE%B1%E2%80%91Diimine%20Ligands&rft.jtitle=Inorganic%20chemistry&rft.au=Wang,%20Peng&rft.aucorp=Univ.%20of%20Utah,%20Salt%20Lake%20City,%20UT%20(United%20States)&rft.date=2021-05-03&rft.volume=60&rft.issue=9&rft.spage=6480&rft.epage=6491&rft.pages=6480-6491&rft.issn=0020-1669&rft.eissn=1520-510X&rft_id=info:doi/10.1021/acs.inorgchem.1c00214&rft_dat=%3Cproquest_osti_%3E2511900904%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2511900904&rft_id=info:pmid/33840189&rfr_iscdi=true |