Synthesis and Structure of Uranium‐Silylene Complexes
While carbene complexes of uranium have been known for over a decade, there are no reported examples of complexes between an actinide and a „heavy carbene.“ Herein, we report the syntheses and structures of the first uranium‐heavy tetrylene complexes: (CpSiMe3)3U‐Si[PhC(NR)2]R’ (R=tBu, R’=NMe2 1; R=...
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creator | Brackbill, I. Joseph Douair, Iskander Lussier, Daniel J. Boreen, Michael A. Maron, Laurent Arnold, John |
description | While carbene complexes of uranium have been known for over a decade, there are no reported examples of complexes between an actinide and a „heavy carbene.“ Herein, we report the syntheses and structures of the first uranium‐heavy tetrylene complexes: (CpSiMe3)3U‐Si[PhC(NR)2]R’ (R=tBu, R’=NMe2 1; R=iPr, R’=PhC(NiPr)2 2). Complex 1 features a kinetically robust uranium‐silicon bonding interaction, while the uranium‐silicon bond in 2 is easily disrupted thermally or by competing ligands in solution. Calculations reveal polarized σ bonds, but depending on the substituents at silicon a substantial π‐bonding interaction is also present. The complexes possess relatively high bond orders which suggests primarily covalent bonding between uranium and silicon. These results comprise a new frontier in actinide‐heavy main‐group bonding.
We have a Si+Uation! Uranium–silylene complexes are reported, representing the first actinide‐heavy tetrylene bonding interactions. Preliminary reactivity studies suggest dative U−Si bonds that can be displaced thermally or with competing ligands. Electronic structure calculations reveal substantial covalent bonding character and even modest π‐bonding (see scheme). |
doi_str_mv | 10.1002/chem.202000214 |
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We have a Si+Uation! Uranium–silylene complexes are reported, representing the first actinide‐heavy tetrylene bonding interactions. Preliminary reactivity studies suggest dative U−Si bonds that can be displaced thermally or with competing ligands. Electronic structure calculations reveal substantial covalent bonding character and even modest π‐bonding (see scheme).</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.202000214</identifier><identifier>PMID: 31950554</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>actinides ; Bonding ; Chemical Physics ; Chemistry ; Covalent bonds ; donor–acceptor interactions ; heavy carbenes ; Physics ; Silicon ; silylenes ; Uranium</subject><ispartof>CHEMISTRY-A EUROPEAN JOURNAL, 2020-02, Vol.26 (11), p.2360-2364</ispartof><rights>2020 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</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-c5774-9f5b6d94c9eee076f73ab6f27452033cc24db942013606933e9181233b971bf43</citedby><cites>FETCH-LOGICAL-c5774-9f5b6d94c9eee076f73ab6f27452033cc24db942013606933e9181233b971bf43</cites><orcidid>0000-0001-9671-227X ; 0000-0003-2653-8557 ; 000000019671227X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.202000214$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.202000214$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,777,781,882,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31950554$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03925210$$DView record in HAL$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1597168$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Brackbill, I. Joseph</creatorcontrib><creatorcontrib>Douair, Iskander</creatorcontrib><creatorcontrib>Lussier, Daniel J.</creatorcontrib><creatorcontrib>Boreen, Michael A.</creatorcontrib><creatorcontrib>Maron, Laurent</creatorcontrib><creatorcontrib>Arnold, John</creatorcontrib><title>Synthesis and Structure of Uranium‐Silylene Complexes</title><title>CHEMISTRY-A EUROPEAN JOURNAL</title><addtitle>Chemistry</addtitle><description>While carbene complexes of uranium have been known for over a decade, there are no reported examples of complexes between an actinide and a „heavy carbene.“ Herein, we report the syntheses and structures of the first uranium‐heavy tetrylene complexes: (CpSiMe3)3U‐Si[PhC(NR)2]R’ (R=tBu, R’=NMe2 1; R=iPr, R’=PhC(NiPr)2 2). Complex 1 features a kinetically robust uranium‐silicon bonding interaction, while the uranium‐silicon bond in 2 is easily disrupted thermally or by competing ligands in solution. Calculations reveal polarized σ bonds, but depending on the substituents at silicon a substantial π‐bonding interaction is also present. The complexes possess relatively high bond orders which suggests primarily covalent bonding between uranium and silicon. These results comprise a new frontier in actinide‐heavy main‐group bonding.
We have a Si+Uation! Uranium–silylene complexes are reported, representing the first actinide‐heavy tetrylene bonding interactions. Preliminary reactivity studies suggest dative U−Si bonds that can be displaced thermally or with competing ligands. Electronic structure calculations reveal substantial covalent bonding character and even modest π‐bonding (see scheme).</description><subject>actinides</subject><subject>Bonding</subject><subject>Chemical Physics</subject><subject>Chemistry</subject><subject>Covalent bonds</subject><subject>donor–acceptor interactions</subject><subject>heavy carbenes</subject><subject>Physics</subject><subject>Silicon</subject><subject>silylenes</subject><subject>Uranium</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqF0U9v0zAYBnBrArGycd0RReMCh3S2X_-Zj1M1KFIRh7KzlbhvVE9JXOxkozc-Ap-RT4KrjCLtwsmy9fMjv34IuWB0zijlV26L3ZxTTvOGiRMyY5KzErSSL8iMGqFLJcGcktcp3WdjFMArcgrMSCqlmBG93vfDFpNPRdVvivUQRzeMEYvQFHex6v3Y_f75a-3bfYs9FovQ7Vr8gemcvGyqNuGbp_WM3H28_bZYlquvnz4vblalk1qL0jSyVhsjnEFEqlWjoapVw7WQnAI4x8WmNoJTBooqA4CGXTMOUBvN6kbAGbmcckMavE3OD-i2LvQ9usEymZW6zujDhLZVa3fRd1Xc21B5u7xZ2cMZBcPzv9AHlu37ye5i-D5iGmznk8O2rXoMY7IcBFMclDCZvntG78MY-zxuVoobwQwcAueTcjGkFLE5voBRe-jIHjqyx47yhbdPsWPd4ebI_5aSgZnAo29x_584u1jefvkX_gdr8Jo7</recordid><startdate>20200221</startdate><enddate>20200221</enddate><creator>Brackbill, I. Joseph</creator><creator>Douair, Iskander</creator><creator>Lussier, Daniel J.</creator><creator>Boreen, Michael A.</creator><creator>Maron, Laurent</creator><creator>Arnold, John</creator><general>Wiley Subscription Services, Inc</general><general>Wiley Blackwell (John Wiley & Sons)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><scope>1XC</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0001-9671-227X</orcidid><orcidid>https://orcid.org/0000-0003-2653-8557</orcidid><orcidid>https://orcid.org/000000019671227X</orcidid></search><sort><creationdate>20200221</creationdate><title>Synthesis and Structure of Uranium‐Silylene Complexes</title><author>Brackbill, I. Joseph ; Douair, Iskander ; Lussier, Daniel J. ; Boreen, Michael A. ; Maron, Laurent ; Arnold, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5774-9f5b6d94c9eee076f73ab6f27452033cc24db942013606933e9181233b971bf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>actinides</topic><topic>Bonding</topic><topic>Chemical Physics</topic><topic>Chemistry</topic><topic>Covalent bonds</topic><topic>donor–acceptor interactions</topic><topic>heavy carbenes</topic><topic>Physics</topic><topic>Silicon</topic><topic>silylenes</topic><topic>Uranium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brackbill, I. Joseph</creatorcontrib><creatorcontrib>Douair, Iskander</creatorcontrib><creatorcontrib>Lussier, Daniel J.</creatorcontrib><creatorcontrib>Boreen, Michael A.</creatorcontrib><creatorcontrib>Maron, Laurent</creatorcontrib><creatorcontrib>Arnold, John</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>OSTI.GOV</collection><jtitle>CHEMISTRY-A EUROPEAN JOURNAL</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brackbill, I. Joseph</au><au>Douair, Iskander</au><au>Lussier, Daniel J.</au><au>Boreen, Michael A.</au><au>Maron, Laurent</au><au>Arnold, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Structure of Uranium‐Silylene Complexes</atitle><jtitle>CHEMISTRY-A EUROPEAN JOURNAL</jtitle><addtitle>Chemistry</addtitle><date>2020-02-21</date><risdate>2020</risdate><volume>26</volume><issue>11</issue><spage>2360</spage><epage>2364</epage><pages>2360-2364</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>While carbene complexes of uranium have been known for over a decade, there are no reported examples of complexes between an actinide and a „heavy carbene.“ Herein, we report the syntheses and structures of the first uranium‐heavy tetrylene complexes: (CpSiMe3)3U‐Si[PhC(NR)2]R’ (R=tBu, R’=NMe2 1; R=iPr, R’=PhC(NiPr)2 2). Complex 1 features a kinetically robust uranium‐silicon bonding interaction, while the uranium‐silicon bond in 2 is easily disrupted thermally or by competing ligands in solution. Calculations reveal polarized σ bonds, but depending on the substituents at silicon a substantial π‐bonding interaction is also present. The complexes possess relatively high bond orders which suggests primarily covalent bonding between uranium and silicon. These results comprise a new frontier in actinide‐heavy main‐group bonding.
We have a Si+Uation! Uranium–silylene complexes are reported, representing the first actinide‐heavy tetrylene bonding interactions. Preliminary reactivity studies suggest dative U−Si bonds that can be displaced thermally or with competing ligands. Electronic structure calculations reveal substantial covalent bonding character and even modest π‐bonding (see scheme).</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31950554</pmid><doi>10.1002/chem.202000214</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9671-227X</orcidid><orcidid>https://orcid.org/0000-0003-2653-8557</orcidid><orcidid>https://orcid.org/000000019671227X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | actinides Bonding Chemical Physics Chemistry Covalent bonds donor–acceptor interactions heavy carbenes Physics Silicon silylenes Uranium |
title | Synthesis and Structure of Uranium‐Silylene Complexes |
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