Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry : a European journal 2024-06, Vol.30 (35), p.e202401358-n/a
Main Authors: Jordan, Emma J., Calder, Ethan D. E., Adcock, Holly V., Male, Louise, Nieger, Martin, Slootweg, J. Chris, Jupp, Andrew R.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c2988-7887b1d09515377e3ada2968ac3e12146606ba3a7e0e2e0e760669f38a81bc083
container_end_page n/a
container_issue 35
container_start_page e202401358
container_title Chemistry : a European journal
container_volume 30
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3039805764</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3039805764</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2988-7887b1d09515377e3ada2968ac3e12146606ba3a7e0e2e0e760669f38a81bc083</originalsourceid><addsrcrecordid>eNqFkE1Lw0AQhhdRbK1ePUrAiwdT9yv74UEooVqh4qF6XjbJlqSk2bqbIPHXu6W1ghcPwzDwzDPDC8AlgmMEIb7LS7MeY4gpRCQRR2CIEoxiwllyDIZQUh6zhMgBOPN-BSGUjJBTMCCCYYopH4KHyZfdlNZvyqox_j5a9E1bGl_522jRui5vO2ci3RRRaq0rqka3lW2iNFytfOv6c3Cy1LU3F_s-Au-P07d0Fs9fn57TyTzOsRQi5kLwDBVQJighnBuiC40lEzonBmFEGYMs00RzAw0OxcPM5JIILVCWQ0FG4Gbn3Tj70RnfqnA_N3WtG2M7rwgkUsCEMxrQ6z_oynauCd8FiklJKKI4UOMdlTvrvTNLtXHVWrteIai2yaptsuqQbFi42mu7bG2KA_4TZQDkDvisatP_o1PpbPryK_8GMRaDQQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3069934142</pqid></control><display><type>article</type><title>Azophosphines: Synthesis, Structure and Coordination Chemistry</title><source>Wiley</source><creator>Jordan, Emma J. ; Calder, Ethan D. E. ; Adcock, Holly V. ; Male, Louise ; Nieger, Martin ; Slootweg, J. Chris ; Jupp, Andrew R.</creator><creatorcontrib>Jordan, Emma J. ; Calder, Ethan D. E. ; Adcock, Holly V. ; Male, Louise ; Nieger, Martin ; Slootweg, J. Chris ; Jupp, Andrew R.</creatorcontrib><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.</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. 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><subject>Azophosphines</subject><subject>Chemical synthesis</subject><subject>Coordination</subject><subject>Coordination Chemistry</subject><subject>Functional groups</subject><subject>Ligands</subject><subject>Main-group Chemistry</subject><subject>Nitrogen</subject><subject>Organic phosphorus</subject><subject>Phosphorus</subject><subject>Ruthenium compounds</subject><issn>0947-6539</issn><issn>1521-3765</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkE1Lw0AQhhdRbK1ePUrAiwdT9yv74UEooVqh4qF6XjbJlqSk2bqbIPHXu6W1ghcPwzDwzDPDC8AlgmMEIb7LS7MeY4gpRCQRR2CIEoxiwllyDIZQUh6zhMgBOPN-BSGUjJBTMCCCYYopH4KHyZfdlNZvyqox_j5a9E1bGl_522jRui5vO2ci3RRRaq0rqka3lW2iNFytfOv6c3Cy1LU3F_s-Au-P07d0Fs9fn57TyTzOsRQi5kLwDBVQJighnBuiC40lEzonBmFEGYMs00RzAw0OxcPM5JIILVCWQ0FG4Gbn3Tj70RnfqnA_N3WtG2M7rwgkUsCEMxrQ6z_oynauCd8FiklJKKI4UOMdlTvrvTNLtXHVWrteIai2yaptsuqQbFi42mu7bG2KA_4TZQDkDvisatP_o1PpbPryK_8GMRaDQQ</recordid><startdate>20240620</startdate><enddate>20240620</enddate><creator>Jordan, Emma J.</creator><creator>Calder, Ethan D. E.</creator><creator>Adcock, Holly V.</creator><creator>Male, Louise</creator><creator>Nieger, Martin</creator><creator>Slootweg, J. Chris</creator><creator>Jupp, Andrew R.</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><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><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></search><sort><creationdate>20240620</creationdate><title>Azophosphines: Synthesis, Structure and Coordination Chemistry</title><author>Jordan, Emma J. ; Calder, Ethan D. E. ; Adcock, Holly V. ; Male, Louise ; Nieger, Martin ; Slootweg, J. Chris ; Jupp, Andrew R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2988-7887b1d09515377e3ada2968ac3e12146606ba3a7e0e2e0e760669f38a81bc083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Azophosphines</topic><topic>Chemical synthesis</topic><topic>Coordination</topic><topic>Coordination Chemistry</topic><topic>Functional groups</topic><topic>Ligands</topic><topic>Main-group Chemistry</topic><topic>Nitrogen</topic><topic>Organic phosphorus</topic><topic>Phosphorus</topic><topic>Ruthenium compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Open Access: Wiley-Blackwell Open Access Journals</collection><collection>Wiley Free Archive</collection><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 &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jordan, Emma J.</au><au>Calder, Ethan D. E.</au><au>Adcock, Holly V.</au><au>Male, Louise</au><au>Nieger, Martin</au><au>Slootweg, J. Chris</au><au>Jupp, Andrew R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Azophosphines: Synthesis, Structure and Coordination Chemistry</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2024-06-20</date><risdate>2024</risdate><volume>30</volume><issue>35</issue><spage>e202401358</spage><epage>n/a</epage><pages>e202401358-n/a</pages><issn>0947-6539</issn><issn>1521-3765</issn><eissn>1521-3765</eissn><abstract>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.</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>
fulltext fulltext
identifier ISSN: 0947-6539
ispartof Chemistry : a European journal, 2024-06, Vol.30 (35), p.e202401358-n/a
issn 0947-6539
1521-3765
1521-3765
language eng
recordid cdi_proquest_miscellaneous_3039805764
source Wiley
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A50%3A46IST&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=Azophosphines:%20Synthesis,%20Structure%20and%20Coordination%20Chemistry&rft.jtitle=Chemistry%20:%20a%20European%20journal&rft.au=Jordan,%20Emma%20J.&rft.date=2024-06-20&rft.volume=30&rft.issue=35&rft.spage=e202401358&rft.epage=n/a&rft.pages=e202401358-n/a&rft.issn=0947-6539&rft.eissn=1521-3765&rft_id=info:doi/10.1002/chem.202401358&rft_dat=%3Cproquest_cross%3E3039805764%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2988-7887b1d09515377e3ada2968ac3e12146606ba3a7e0e2e0e760669f38a81bc083%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3069934142&rft_id=info:pmid/38624247&rfr_iscdi=true