Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes
Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. An X-ray crystallographic analysis shows the m...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-01, Vol.60 (8), p.1016-1019 |
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creator | Mondal, Rahul Evans, Matthew J Nguyen, Dat T Thayalan Rajeshkumar Maron, Laurent Jones, Cameron |
description | Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. An X-ray crystallographic analysis shows the molecule to contain a very long Mg–Mg bond (3.137(2) Å). The formation of [{K(TripNON)Mg}2] contrasts with a previously reported reduction of a magnesium(ii) complex incorporating a bulkier diamide ligand, which instead afforded a magnesium–dinitrogen complex. In the current study, [{K(TripNON)Mg}2] has been shown to be a viable reagent for the reductive activation of CO, H2 and N2O. |
doi_str_mv | 10.1039/d3cc05787a |
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An X-ray crystallographic analysis shows the molecule to contain a very long Mg–Mg bond (3.137(2) Å). The formation of [{K(TripNON)Mg}2] contrasts with a previously reported reduction of a magnesium(ii) complex incorporating a bulkier diamide ligand, which instead afforded a magnesium–dinitrogen complex. In the current study, [{K(TripNON)Mg}2] has been shown to be a viable reagent for the reductive activation of CO, H2 and N2O.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d3cc05787a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Chemical reduction ; Chemical Sciences ; Crystallography ; Magnesium ; Nitrogen compounds ; Potassium salts ; Reagents</subject><ispartof>Chemical communications (Cambridge, England), 2024-01, Vol.60 (8), p.1016-1019</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-2653-8557</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04707627$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mondal, Rahul</creatorcontrib><creatorcontrib>Evans, Matthew J</creatorcontrib><creatorcontrib>Nguyen, Dat T</creatorcontrib><creatorcontrib>Thayalan Rajeshkumar</creatorcontrib><creatorcontrib>Maron, Laurent</creatorcontrib><creatorcontrib>Jones, Cameron</creatorcontrib><title>Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes</title><title>Chemical communications (Cambridge, England)</title><description>Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. An X-ray crystallographic analysis shows the molecule to contain a very long Mg–Mg bond (3.137(2) Å). The formation of [{K(TripNON)Mg}2] contrasts with a previously reported reduction of a magnesium(ii) complex incorporating a bulkier diamide ligand, which instead afforded a magnesium–dinitrogen complex. In the current study, [{K(TripNON)Mg}2] has been shown to be a viable reagent for the reductive activation of CO, H2 and N2O.</description><subject>Chemical reduction</subject><subject>Chemical Sciences</subject><subject>Crystallography</subject><subject>Magnesium</subject><subject>Nitrogen compounds</subject><subject>Potassium salts</subject><subject>Reagents</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkL9OwzAQhyMEEqWw8ASWWGBIseP_Y1UBRWphACS26OK4rUsShzip6MY78IY8CSll4pY7ffruJ91F0TnBI4Kpvs6pMZhLJeEgGhAqWMyZej3czVzHkjJ-HJ2EsMZ9Ea4GUf3U2sYZZHzVNr5AfoHmy-_Pr_kSZb7K0cI3JbTOV2gTRughQWBat9kTV6F2ZVFj8878gn4564q3LSphWdnguhLlDkqX2z6_rAv7YcNpdLSAItizvz6MXm5vnifTePZ4dz8Zz-JVwnEbCwlAMiyEzBRQoSk1CQOdZVpRrLnOcgNMMQEAgiZaY0ZzAUQKIlUGitJhdLXPXUGR1o0rodmmHlw6Hc_SHcNMYikSuSG9e7l368a_dza0aemCsUUBlfVdSBNNMFFac96rF__Ute-aqr9kZ8n-24xR-gPs2nej</recordid><startdate>20240123</startdate><enddate>20240123</enddate><creator>Mondal, Rahul</creator><creator>Evans, Matthew J</creator><creator>Nguyen, Dat T</creator><creator>Thayalan Rajeshkumar</creator><creator>Maron, Laurent</creator><creator>Jones, Cameron</creator><general>Royal Society of Chemistry</general><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-2653-8557</orcidid></search><sort><creationdate>20240123</creationdate><title>Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes</title><author>Mondal, Rahul ; Evans, Matthew J ; Nguyen, Dat T ; Thayalan Rajeshkumar ; Maron, Laurent ; Jones, Cameron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h250t-67aa1b0667b8a36933c24a9bb9830959bdca4846aaa63299043d6a176178ba833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Chemical reduction</topic><topic>Chemical Sciences</topic><topic>Crystallography</topic><topic>Magnesium</topic><topic>Nitrogen compounds</topic><topic>Potassium salts</topic><topic>Reagents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mondal, Rahul</creatorcontrib><creatorcontrib>Evans, Matthew J</creatorcontrib><creatorcontrib>Nguyen, Dat T</creatorcontrib><creatorcontrib>Thayalan Rajeshkumar</creatorcontrib><creatorcontrib>Maron, Laurent</creatorcontrib><creatorcontrib>Jones, Cameron</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mondal, Rahul</au><au>Evans, Matthew J</au><au>Nguyen, Dat T</au><au>Thayalan Rajeshkumar</au><au>Maron, Laurent</au><au>Jones, Cameron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2024-01-23</date><risdate>2024</risdate><volume>60</volume><issue>8</issue><spage>1016</spage><epage>1019</epage><pages>1016-1019</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. 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subjects | Chemical reduction Chemical Sciences Crystallography Magnesium Nitrogen compounds Potassium salts Reagents |
title | Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes |
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