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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...
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Published in: | Journal of organic chemistry 2007-10, Vol.72 (22), p.8186-8195 |
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container_end_page | 8195 |
container_issue | 22 |
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container_title | Journal of organic chemistry |
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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 |
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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. 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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> |
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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 |
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