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Azophosphines: Synthesis, Structure and Coordination Chemistry
The conceptual replacement of nitrogen with phosphorus in common organic functional groups unlocks new properties and reactivity. The phosphorus‐containing analogues of triazenes are underexplored but offer great potential as flexible and small bite‐angle ligands. This manuscript explores the synthe...
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Published in: | Chemistry : a European journal 2024-06, Vol.30 (35), p.e202401358-n/a |
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creator | Jordan, Emma J. Calder, Ethan D. E. Adcock, Holly V. Male, Louise Nieger, Martin Slootweg, J. Chris Jupp, Andrew R. |
description | The conceptual replacement of nitrogen with phosphorus in common organic functional groups unlocks new properties and reactivity. The phosphorus‐containing analogues of triazenes are underexplored but offer great potential as flexible and small bite‐angle ligands. This manuscript explores the synthesis and characterisation of a family of air‐stable azophosphine‐borane complexes, and their subsequent deprotection to the free azophosphines. These compounds are structurally characterised, both experimentally and computationally, and highlight the availability of the phosphorus lone pair for coordination. This is confirmed by demonstrating that neutral azophosphines can act as ligands in Ru complexes, and can coordinate as monodentate or bidentate ligands in a controlled manner, in contrast to their nitrogen analogues.
Functional groups are fundamentally important for synthetic chemists and enable rational understanding of reactivity. Azophosphines are underexplored compounds that are heavier congeners of triazenes, and we have devised a general synthesis to this family of compounds. The availability of the phosphorus lone pair enabled them to be used as ligands that can bind in different coordination modes in a controlled manner. |
doi_str_mv | 10.1002/chem.202401358 |
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Functional groups are fundamentally important for synthetic chemists and enable rational understanding of reactivity. Azophosphines are underexplored compounds that are heavier congeners of triazenes, and we have devised a general synthesis to this family of compounds. The availability of the phosphorus lone pair enabled them to be used as ligands that can bind in different coordination modes in a controlled manner.</description><identifier>ISSN: 0947-6539</identifier><identifier>ISSN: 1521-3765</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.202401358</identifier><identifier>PMID: 38624247</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Azophosphines ; Chemical synthesis ; Coordination ; Coordination Chemistry ; Functional groups ; Ligands ; Main-group Chemistry ; Nitrogen ; Organic phosphorus ; Phosphorus ; Ruthenium compounds</subject><ispartof>Chemistry : a European journal, 2024-06, Vol.30 (35), p.e202401358-n/a</ispartof><rights>2024 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH</rights><rights>2024 Wiley‐VCH GmbH.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2988-7887b1d09515377e3ada2968ac3e12146606ba3a7e0e2e0e760669f38a81bc083</cites><orcidid>0000-0002-8295-2528 ; 0000-0003-1677-0109 ; 0009-0005-5440-0418 ; 0000-0001-7818-7766 ; 0000-0003-4360-5838 ; 0009-0003-6748-322X ; 0000-0003-1214-1460</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38624247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jordan, Emma J.</creatorcontrib><creatorcontrib>Calder, Ethan D. E.</creatorcontrib><creatorcontrib>Adcock, Holly V.</creatorcontrib><creatorcontrib>Male, Louise</creatorcontrib><creatorcontrib>Nieger, Martin</creatorcontrib><creatorcontrib>Slootweg, J. Chris</creatorcontrib><creatorcontrib>Jupp, Andrew R.</creatorcontrib><title>Azophosphines: Synthesis, Structure and Coordination Chemistry</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>The conceptual replacement of nitrogen with phosphorus in common organic functional groups unlocks new properties and reactivity. The phosphorus‐containing analogues of triazenes are underexplored but offer great potential as flexible and small bite‐angle ligands. This manuscript explores the synthesis and characterisation of a family of air‐stable azophosphine‐borane complexes, and their subsequent deprotection to the free azophosphines. These compounds are structurally characterised, both experimentally and computationally, and highlight the availability of the phosphorus lone pair for coordination. This is confirmed by demonstrating that neutral azophosphines can act as ligands in Ru complexes, and can coordinate as monodentate or bidentate ligands in a controlled manner, in contrast to their nitrogen analogues.
Functional groups are fundamentally important for synthetic chemists and enable rational understanding of reactivity. Azophosphines are underexplored compounds that are heavier congeners of triazenes, and we have devised a general synthesis to this family of compounds. 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These compounds are structurally characterised, both experimentally and computationally, and highlight the availability of the phosphorus lone pair for coordination. This is confirmed by demonstrating that neutral azophosphines can act as ligands in Ru complexes, and can coordinate as monodentate or bidentate ligands in a controlled manner, in contrast to their nitrogen analogues.
Functional groups are fundamentally important for synthetic chemists and enable rational understanding of reactivity. Azophosphines are underexplored compounds that are heavier congeners of triazenes, and we have devised a general synthesis to this family of compounds. The availability of the phosphorus lone pair enabled them to be used as ligands that can bind in different coordination modes in a controlled manner.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38624247</pmid><doi>10.1002/chem.202401358</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-8295-2528</orcidid><orcidid>https://orcid.org/0000-0003-1677-0109</orcidid><orcidid>https://orcid.org/0009-0005-5440-0418</orcidid><orcidid>https://orcid.org/0000-0001-7818-7766</orcidid><orcidid>https://orcid.org/0000-0003-4360-5838</orcidid><orcidid>https://orcid.org/0009-0003-6748-322X</orcidid><orcidid>https://orcid.org/0000-0003-1214-1460</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Azophosphines Chemical synthesis Coordination Coordination Chemistry Functional groups Ligands Main-group Chemistry Nitrogen Organic phosphorus Phosphorus Ruthenium compounds |
title | Azophosphines: Synthesis, Structure and Coordination Chemistry |
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