Ionisation Chimique de Composés Aromatiques Nitrés
Les dissociation induites par collisions d'ions [MH‐30]+ observés lors de l'ionization chimique (méthane) de composés aromatiques nitrés indiquent que ces ions sont formés par réduction suivie de protonation et non par perte de NO⋅ des ions moléculaires protonés. The collision induced diss...
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| Veröffentlicht in: | Organic Mass Spectrometry 1979-02, Vol.14 (2), p.117-118 |
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| container_title | Organic Mass Spectrometry |
| container_volume | 14 |
| creator | Maquestiau, A. Van Haverbeke, Y. Flammang, R. Mispreuve, H. Elguero, J. |
| description | Les dissociation induites par collisions d'ions [MH‐30]+ observés lors de l'ionization chimique (méthane) de composés aromatiques nitrés indiquent que ces ions sont formés par réduction suivie de protonation et non par perte de NO⋅ des ions moléculaires protonés.
The collision induced dissociations of [MH – 30]+ ions observed in the chemical ionization (methane) mass spectra of some nitro aromatic compounds show that these ions are formed by reduction in the ion source with subsequent protonation and not by the previously reported losses of NO· from the protonated molecular ions. |
| doi_str_mv | 10.1002/oms.1210140212 |
| format | Article |
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The collision induced dissociations of [MH – 30]+ ions observed in the chemical ionization (methane) mass spectra of some nitro aromatic compounds show that these ions are formed by reduction in the ion source with subsequent protonation and not by the previously reported losses of NO· from the protonated molecular ions.</description><identifier>ISSN: 0030-493X</identifier><identifier>EISSN: 1096-9888</identifier><identifier>DOI: 10.1002/oms.1210140212</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><ispartof>Organic Mass Spectrometry, 1979-02, Vol.14 (2), p.117-118</ispartof><rights>Copyright © 1979 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1342-e50bd9357108ec42c23795b7f68450ba3616abec73c220255e74696d2ea662f03</citedby><cites>FETCH-LOGICAL-c1342-e50bd9357108ec42c23795b7f68450ba3616abec73c220255e74696d2ea662f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Foms.1210140212$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Foms.1210140212$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids></links><search><creatorcontrib>Maquestiau, A.</creatorcontrib><creatorcontrib>Van Haverbeke, Y.</creatorcontrib><creatorcontrib>Flammang, R.</creatorcontrib><creatorcontrib>Mispreuve, H.</creatorcontrib><creatorcontrib>Elguero, J.</creatorcontrib><title>Ionisation Chimique de Composés Aromatiques Nitrés</title><title>Organic Mass Spectrometry</title><description>Les dissociation induites par collisions d'ions [MH‐30]+ observés lors de l'ionization chimique (méthane) de composés aromatiques nitrés indiquent que ces ions sont formés par réduction suivie de protonation et non par perte de NO⋅ des ions moléculaires protonés.
The collision induced dissociations of [MH – 30]+ ions observed in the chemical ionization (methane) mass spectra of some nitro aromatic compounds show that these ions are formed by reduction in the ion source with subsequent protonation and not by the previously reported losses of NO· from the protonated molecular ions.</description><issn>0030-493X</issn><issn>1096-9888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><recordid>eNqFj81KAzEUhYMoOFa3rucFZry5yWQmyzL4U6jtQgV3IZPJYKTT1KQifSSfwxczUsHuXF0453wXPkIuKZQUAK_8GEuKFCgHpHhEMgpSFLJpmmOSATAouGTPp-QsxlcAkJKLjPCZX7uot86v8_bFje7t3ea9zVs_bnz8-oz5NPgx9SmP-cJtQ8rOycmgV9Fe_N4Jebq5fmzvivnydtZO54WhjGNhK-h6yaqaQmMNR4OsllVXD6LhqdJMUKE7a2pmEAGrytZcSNGj1ULgAGxCyv1fE3yMwQ5qE9yow05RUD_OKjmrP-cEyD3w4VZ2989aLe8fDthvUTZbAw</recordid><startdate>197902</startdate><enddate>197902</enddate><creator>Maquestiau, A.</creator><creator>Van Haverbeke, Y.</creator><creator>Flammang, R.</creator><creator>Mispreuve, H.</creator><creator>Elguero, J.</creator><general>John Wiley & Sons, Ltd</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>197902</creationdate><title>Ionisation Chimique de Composés Aromatiques Nitrés</title><author>Maquestiau, A. ; Van Haverbeke, Y. ; Flammang, R. ; Mispreuve, H. ; Elguero, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1342-e50bd9357108ec42c23795b7f68450ba3616abec73c220255e74696d2ea662f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maquestiau, A.</creatorcontrib><creatorcontrib>Van Haverbeke, Y.</creatorcontrib><creatorcontrib>Flammang, R.</creatorcontrib><creatorcontrib>Mispreuve, H.</creatorcontrib><creatorcontrib>Elguero, J.</creatorcontrib><collection>CrossRef</collection><jtitle>Organic Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maquestiau, A.</au><au>Van Haverbeke, Y.</au><au>Flammang, R.</au><au>Mispreuve, H.</au><au>Elguero, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ionisation Chimique de Composés Aromatiques Nitrés</atitle><jtitle>Organic Mass Spectrometry</jtitle><date>1979-02</date><risdate>1979</risdate><volume>14</volume><issue>2</issue><spage>117</spage><epage>118</epage><pages>117-118</pages><issn>0030-493X</issn><eissn>1096-9888</eissn><abstract>Les dissociation induites par collisions d'ions [MH‐30]+ observés lors de l'ionization chimique (méthane) de composés aromatiques nitrés indiquent que ces ions sont formés par réduction suivie de protonation et non par perte de NO⋅ des ions moléculaires protonés.
The collision induced dissociations of [MH – 30]+ ions observed in the chemical ionization (methane) mass spectra of some nitro aromatic compounds show that these ions are formed by reduction in the ion source with subsequent protonation and not by the previously reported losses of NO· from the protonated molecular ions.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/oms.1210140212</doi><tpages>2</tpages></addata></record> |
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| source | Wiley Online Library - AutoHoldings Journals |
| title | Ionisation Chimique de Composés Aromatiques Nitrés |
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