Loading…

Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies

Laser flash photolysis of 1-(carbazol-9-yl)-2,4,6-trimethylpyridinium tetrafluoroborate generates the carbazolyl nitrenium ion (τ = 333 ns, k obs = 3.0 × 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN. The nitrenium ion is found to have reactivity comparable to structurally similar c...

Full description

Saved in:
Bibliographic Details
Published in:Journal of organic chemistry 2007-10, Vol.72 (22), p.8186-8195
Main Authors: Winter, Arthur H, Gibson, Harry H, Falvey, Daniel E
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3
cites cdi_FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3
container_end_page 8195
container_issue 22
container_start_page 8186
container_title Journal of organic chemistry
container_volume 72
creator Winter, Arthur H
Gibson, Harry H
Falvey, Daniel E
description Laser flash photolysis of 1-(carbazol-9-yl)-2,4,6-trimethylpyridinium tetrafluoroborate generates the carbazolyl nitrenium ion (τ = 333 ns, k obs = 3.0 × 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN. The nitrenium ion is found to have reactivity comparable to structurally similar closed-shell diarylnitrenium ions, but spectroscopic evidence favors an open-shell singlet diradical assignment for the observed nitrenium ion. The carbazolyl nitrenium ion is also more reactive than diarylnitrenium ions as a likely result of antiaromatic character. Ab initio and hybrid DFT calculations were performed to address the degree of antiaromaticity in this and similar nitrenium ions through analysis of optimized geometries, nucleus independent chemical shifts, and isodesmic reactions.
doi_str_mv 10.1021/jo0708184
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68405227</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68405227</sourcerecordid><originalsourceid>FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3</originalsourceid><addsrcrecordid>eNptkc9u1DAQhy0EokvhwAsgX0BCImA7_3tbRS1ttYIVu3CNJo7duiRx8DgSy4krb8Mz8SR42ah7wbJk2fPpm5F_hDzn7C1ngr-7syxnBS-SB2TBU8GirGTJQ7JgTIgoFll8Qp4g3rGw0jR9TE54XpRClMWC_K7ANfDDdruOfjDeqcFMPb2yw9mfn7_oeaekd3aglR20uZkceBNuMLR0OXgDzvbhRRq_o0tEFXZLmx1dASpHLzrAW7q-tT7Y0eAbunUwjma4oZ_Aq70TPQw-FNbOtpP0QQozum9R2X6c_L-W0NGNn1qj8Cl5pKFD9Ww-T8nni_NtdRmtPr6_qparCOKC-4gLLVtQUmcFgNStTllZtA1LM1aCzlncyKLUSkjRlEnDmYZMaqFYErdxo7iMT8mrg3d09tuk0Ne9Qam6DgZlJ6yzImGpEHkAXx9A6SyiU7oenenB7WrO6n089X08gX0xS6emV-2RnPMIwMsZAJTQaQeDNHjkSl7GeZEFLjpwBr36fl8H97XO8jhP6-16U19vLtNVmVzXX45ekBjmmVz4UfzPgH8BsKy4Og</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68405227</pqid></control><display><type>article</type><title>Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Winter, Arthur H ; Gibson, Harry H ; Falvey, Daniel E</creator><creatorcontrib>Winter, Arthur H ; Gibson, Harry H ; Falvey, Daniel E</creatorcontrib><description>Laser flash photolysis of 1-(carbazol-9-yl)-2,4,6-trimethylpyridinium tetrafluoroborate generates the carbazolyl nitrenium ion (τ = 333 ns, k obs = 3.0 × 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN. The nitrenium ion is found to have reactivity comparable to structurally similar closed-shell diarylnitrenium ions, but spectroscopic evidence favors an open-shell singlet diradical assignment for the observed nitrenium ion. The carbazolyl nitrenium ion is also more reactive than diarylnitrenium ions as a likely result of antiaromatic character. Ab initio and hybrid DFT calculations were performed to address the degree of antiaromaticity in this and similar nitrenium ions through analysis of optimized geometries, nucleus independent chemical shifts, and isodesmic reactions.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo0708184</identifier><identifier>PMID: 17892298</identifier><identifier>CODEN: JOCEAH</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Chemical reactivity ; Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with only one n hetero atom and condensed derivatives ; Organic chemistry ; Preparations and properties ; Reactivity and mechanisms</subject><ispartof>Journal of organic chemistry, 2007-10, Vol.72 (22), p.8186-8195</ispartof><rights>Copyright © 2007 American Chemical Society</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3</citedby><cites>FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19193786$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17892298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Winter, Arthur H</creatorcontrib><creatorcontrib>Gibson, Harry H</creatorcontrib><creatorcontrib>Falvey, Daniel E</creatorcontrib><title>Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Laser flash photolysis of 1-(carbazol-9-yl)-2,4,6-trimethylpyridinium tetrafluoroborate generates the carbazolyl nitrenium ion (τ = 333 ns, k obs = 3.0 × 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN. The nitrenium ion is found to have reactivity comparable to structurally similar closed-shell diarylnitrenium ions, but spectroscopic evidence favors an open-shell singlet diradical assignment for the observed nitrenium ion. The carbazolyl nitrenium ion is also more reactive than diarylnitrenium ions as a likely result of antiaromatic character. Ab initio and hybrid DFT calculations were performed to address the degree of antiaromaticity in this and similar nitrenium ions through analysis of optimized geometries, nucleus independent chemical shifts, and isodesmic reactions.</description><subject>Chemical reactivity</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with only one n hetero atom and condensed derivatives</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Reactivity and mechanisms</subject><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNptkc9u1DAQhy0EokvhwAsgX0BCImA7_3tbRS1ttYIVu3CNJo7duiRx8DgSy4krb8Mz8SR42ah7wbJk2fPpm5F_hDzn7C1ngr-7syxnBS-SB2TBU8GirGTJQ7JgTIgoFll8Qp4g3rGw0jR9TE54XpRClMWC_K7ANfDDdruOfjDeqcFMPb2yw9mfn7_oeaekd3aglR20uZkceBNuMLR0OXgDzvbhRRq_o0tEFXZLmx1dASpHLzrAW7q-tT7Y0eAbunUwjma4oZ_Aq70TPQw-FNbOtpP0QQozum9R2X6c_L-W0NGNn1qj8Cl5pKFD9Ww-T8nni_NtdRmtPr6_qparCOKC-4gLLVtQUmcFgNStTllZtA1LM1aCzlncyKLUSkjRlEnDmYZMaqFYErdxo7iMT8mrg3d09tuk0Ne9Qam6DgZlJ6yzImGpEHkAXx9A6SyiU7oenenB7WrO6n089X08gX0xS6emV-2RnPMIwMsZAJTQaQeDNHjkSl7GeZEFLjpwBr36fl8H97XO8jhP6-16U19vLtNVmVzXX45ekBjmmVz4UfzPgH8BsKy4Og</recordid><startdate>20071026</startdate><enddate>20071026</enddate><creator>Winter, Arthur H</creator><creator>Gibson, Harry H</creator><creator>Falvey, Daniel E</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20071026</creationdate><title>Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies</title><author>Winter, Arthur H ; Gibson, Harry H ; Falvey, Daniel E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Chemical reactivity</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with only one n hetero atom and condensed derivatives</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><topic>Reactivity and mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Winter, Arthur H</creatorcontrib><creatorcontrib>Gibson, Harry H</creatorcontrib><creatorcontrib>Falvey, Daniel E</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Winter, Arthur H</au><au>Gibson, Harry H</au><au>Falvey, Daniel E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2007-10-26</date><risdate>2007</risdate><volume>72</volume><issue>22</issue><spage>8186</spage><epage>8195</epage><pages>8186-8195</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>Laser flash photolysis of 1-(carbazol-9-yl)-2,4,6-trimethylpyridinium tetrafluoroborate generates the carbazolyl nitrenium ion (τ = 333 ns, k obs = 3.0 × 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN. The nitrenium ion is found to have reactivity comparable to structurally similar closed-shell diarylnitrenium ions, but spectroscopic evidence favors an open-shell singlet diradical assignment for the observed nitrenium ion. The carbazolyl nitrenium ion is also more reactive than diarylnitrenium ions as a likely result of antiaromatic character. Ab initio and hybrid DFT calculations were performed to address the degree of antiaromaticity in this and similar nitrenium ions through analysis of optimized geometries, nucleus independent chemical shifts, and isodesmic reactions.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17892298</pmid><doi>10.1021/jo0708184</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3263
ispartof Journal of organic chemistry, 2007-10, Vol.72 (22), p.8186-8195
issn 0022-3263
1520-6904
language eng
recordid cdi_proquest_miscellaneous_68405227
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Chemical reactivity
Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with only one n hetero atom and condensed derivatives
Organic chemistry
Preparations and properties
Reactivity and mechanisms
title Carbazolyl Nitrenium Ion:  Electron Configuration and Antiaromaticity Assessed by Laser Flash Photolysis, Trapping Rate Constants, Product Analysis, and Computational Studies
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T15%3A36%3A23IST&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=Carbazolyl%20Nitrenium%20Ion:%E2%80%89%20Electron%20Configuration%20and%20Antiaromaticity%20Assessed%20by%20Laser%20Flash%20Photolysis,%20Trapping%20Rate%20Constants,%20Product%20Analysis,%20and%20Computational%20Studies&rft.jtitle=Journal%20of%20organic%20chemistry&rft.au=Winter,%20Arthur%20H&rft.date=2007-10-26&rft.volume=72&rft.issue=22&rft.spage=8186&rft.epage=8195&rft.pages=8186-8195&rft.issn=0022-3263&rft.eissn=1520-6904&rft.coden=JOCEAH&rft_id=info:doi/10.1021/jo0708184&rft_dat=%3Cproquest_cross%3E68405227%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a381t-12fcdaecf68aacfdf5098db05609af703bc89fe2c2b94b10fa6cf2e043d3be1c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=68405227&rft_id=info:pmid/17892298&rfr_iscdi=true