Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair
Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to th...
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2009-01 (7), p.830-832 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 832 |
---|---|
container_issue | 7 |
container_start_page | 830 |
container_title | Chemical communications (Cambridge, England) |
container_volume | |
creator | Schmid, Dirk Loscher, Sebastian Gudat, Dietrich Bubrin, Denis Hartenbach, Ingo Schleid, Thomas Benko, Zoltán Nyulászi, László |
description | Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to their ionic nature. |
doi_str_mv | 10.1039/b817046k |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67071198</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67071198</sourcerecordid><originalsourceid>FETCH-LOGICAL-c281t-3bc02be8e514fe658e59edef62e0360590aa6c0a0f2f5cb71faabc08191cef793</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EoqUg8QtQJsRQgx3HTsxGK75EJRaQ2CLHOQuXJA52MtBfj6tWYuKk0z3Dc-_wInROyTUlTN5UBc1JJr4O0JQykWGeFR-HW-YS5yzjE3QSwprEobw4RhMqWZpmXEzRegHdxmE6Z_MU11ZtVP_pQtzG1pCork6qf4WxvY1GYoODBvTgXWd1orxr1bCFzroO68iuS3pl_Sk6MqoJcLa_M_T-cP-2fMKr18fn5d0K67SgA2aVJmkFBXCaGRA8goQajEiBMEG4JEoJTRQxqeG6yqlRKr4UVFINJpdshi53ub133yOEoWxt0NA0qgM3hlLkJKdUFlG82onauxA8mLL3tlX-p6Sk3PZaLna9vkT1Yp85Vi3Uf-K-SPYLqTpzWg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67071198</pqid></control><display><type>article</type><title>Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Schmid, Dirk ; Loscher, Sebastian ; Gudat, Dietrich ; Bubrin, Denis ; Hartenbach, Ingo ; Schleid, Thomas ; Benko, Zoltán ; Nyulászi, László</creator><creatorcontrib>Schmid, Dirk ; Loscher, Sebastian ; Gudat, Dietrich ; Bubrin, Denis ; Hartenbach, Ingo ; Schleid, Thomas ; Benko, Zoltán ; Nyulászi, László</creatorcontrib><description>Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to their ionic nature.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/b817046k</identifier><identifier>PMID: 19322456</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2009-01 (7), p.830-832</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-3bc02be8e514fe658e59edef62e0360590aa6c0a0f2f5cb71faabc08191cef793</citedby><cites>FETCH-LOGICAL-c281t-3bc02be8e514fe658e59edef62e0360590aa6c0a0f2f5cb71faabc08191cef793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19322456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmid, Dirk</creatorcontrib><creatorcontrib>Loscher, Sebastian</creatorcontrib><creatorcontrib>Gudat, Dietrich</creatorcontrib><creatorcontrib>Bubrin, Denis</creatorcontrib><creatorcontrib>Hartenbach, Ingo</creatorcontrib><creatorcontrib>Schleid, Thomas</creatorcontrib><creatorcontrib>Benko, Zoltán</creatorcontrib><creatorcontrib>Nyulászi, László</creatorcontrib><title>Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to their ionic nature.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp1kD1PwzAQhi0EoqUg8QtQJsRQgx3HTsxGK75EJRaQ2CLHOQuXJA52MtBfj6tWYuKk0z3Dc-_wInROyTUlTN5UBc1JJr4O0JQykWGeFR-HW-YS5yzjE3QSwprEobw4RhMqWZpmXEzRegHdxmE6Z_MU11ZtVP_pQtzG1pCork6qf4WxvY1GYoODBvTgXWd1orxr1bCFzroO68iuS3pl_Sk6MqoJcLa_M_T-cP-2fMKr18fn5d0K67SgA2aVJmkFBXCaGRA8goQajEiBMEG4JEoJTRQxqeG6yqlRKr4UVFINJpdshi53ub133yOEoWxt0NA0qgM3hlLkJKdUFlG82onauxA8mLL3tlX-p6Sk3PZaLna9vkT1Yp85Vi3Uf-K-SPYLqTpzWg</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Schmid, Dirk</creator><creator>Loscher, Sebastian</creator><creator>Gudat, Dietrich</creator><creator>Bubrin, Denis</creator><creator>Hartenbach, Ingo</creator><creator>Schleid, Thomas</creator><creator>Benko, Zoltán</creator><creator>Nyulászi, László</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair</title><author>Schmid, Dirk ; Loscher, Sebastian ; Gudat, Dietrich ; Bubrin, Denis ; Hartenbach, Ingo ; Schleid, Thomas ; Benko, Zoltán ; Nyulászi, László</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-3bc02be8e514fe658e59edef62e0360590aa6c0a0f2f5cb71faabc08191cef793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmid, Dirk</creatorcontrib><creatorcontrib>Loscher, Sebastian</creatorcontrib><creatorcontrib>Gudat, Dietrich</creatorcontrib><creatorcontrib>Bubrin, Denis</creatorcontrib><creatorcontrib>Hartenbach, Ingo</creatorcontrib><creatorcontrib>Schleid, Thomas</creatorcontrib><creatorcontrib>Benko, Zoltán</creatorcontrib><creatorcontrib>Nyulászi, László</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmid, Dirk</au><au>Loscher, Sebastian</au><au>Gudat, Dietrich</au><au>Bubrin, Denis</au><au>Hartenbach, Ingo</au><au>Schleid, Thomas</au><au>Benko, Zoltán</au><au>Nyulászi, László</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2009-01-01</date><risdate>2009</risdate><issue>7</issue><spage>830</spage><epage>832</epage><pages>830-832</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to their ionic nature.</abstract><cop>England</cop><pmid>19322456</pmid><doi>10.1039/b817046k</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2009-01 (7), p.830-832 |
issn | 1359-7345 1364-548X |
language | eng |
recordid | cdi_proquest_miscellaneous_67071198 |
source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
title | Benzo-1,3,2-diazaphospholide and benzo-1,3,2-diazaphospholium: an isoelectronic aromatic anion-cation pair |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-04T19%3A23%3A03IST&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=Benzo-1,3,2-diazaphospholide%20and%20benzo-1,3,2-diazaphospholium:%20an%20isoelectronic%20aromatic%20anion-cation%20pair&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Schmid,%20Dirk&rft.date=2009-01-01&rft.issue=7&rft.spage=830&rft.epage=832&rft.pages=830-832&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/b817046k&rft_dat=%3Cproquest_cross%3E67071198%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67071198&rft_id=info:pmid/19322456&rfr_iscdi=true |