Mass spectrometric indication of double bond position in dodecenals without any chemical derivatization
Ten positional isomers (Δ2‐Δ11) of unmodified dodecenal were analysed by conventional combined gas chromatography/electron impact mass spectrometry. The relative abundances of some predominant fragments in the isomers examined varied with the position of the original double bond. Eminent dominance o...
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Veröffentlicht in: | Biological Mass Spectrometry 1988-10, Vol.17 (4), p.301-306 |
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creator | Horiike, Michio Hirano, Chisato |
description | Ten positional isomers (Δ2‐Δ11) of unmodified dodecenal were analysed by conventional combined gas chromatography/electron impact mass spectrometry. The relative abundances of some predominant fragments in the isomers examined varied with the position of the original double bond. Eminent dominance of a particular isomer over the others in their relative intensities was observed at some fragment ion peaks. The intensity ratios of certain selected pairs of predominant fragment ions are of diagnostic value for the identification of the double bond position. A procedure for the characterization of the double bond position in the chain is given. |
doi_str_mv | 10.1002/bms.1200170413 |
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The relative abundances of some predominant fragments in the isomers examined varied with the position of the original double bond. Eminent dominance of a particular isomer over the others in their relative intensities was observed at some fragment ion peaks. The intensity ratios of certain selected pairs of predominant fragment ions are of diagnostic value for the identification of the double bond position. A procedure for the characterization of the double bond position in the chain is given.</description><identifier>ISSN: 1052-9306</identifier><identifier>ISSN: 0887-6134</identifier><identifier>EISSN: 1096-9888</identifier><identifier>EISSN: 2376-3868</identifier><identifier>DOI: 10.1002/bms.1200170413</identifier><identifier>CODEN: BEMSEN</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Chemistry ; Exact sciences and technology ; Mass spectrometry ; Organic chemistry ; Reactivity and mechanisms</subject><ispartof>Biological Mass Spectrometry, 1988-10, Vol.17 (4), p.301-306</ispartof><rights>Copyright © 1988 John Wiley & Sons Ltd.</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4223-592c792fac8b53a345ec70319655f32f2308190c1b4fb15ec043673b99b61c2d3</citedby><cites>FETCH-LOGICAL-c4223-592c792fac8b53a345ec70319655f32f2308190c1b4fb15ec043673b99b61c2d3</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%2Fbms.1200170413$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbms.1200170413$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6592901$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Horiike, Michio</creatorcontrib><creatorcontrib>Hirano, Chisato</creatorcontrib><title>Mass spectrometric indication of double bond position in dodecenals without any chemical derivatization</title><title>Biological Mass Spectrometry</title><addtitle>Biol. Mass Spectrom</addtitle><description>Ten positional isomers (Δ2‐Δ11) of unmodified dodecenal were analysed by conventional combined gas chromatography/electron impact mass spectrometry. The relative abundances of some predominant fragments in the isomers examined varied with the position of the original double bond. Eminent dominance of a particular isomer over the others in their relative intensities was observed at some fragment ion peaks. The intensity ratios of certain selected pairs of predominant fragment ions are of diagnostic value for the identification of the double bond position. A procedure for the characterization of the double bond position in the chain is given.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Mass spectrometry</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><issn>1052-9306</issn><issn>0887-6134</issn><issn>1096-9888</issn><issn>2376-3868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEUhYMoWKtb11m4nXqTzCtLLVqFVsUHQjchk8nY6LxIptb66007orhydS835zs5HISOCYwIAD3NKjciFIAkEBK2gwYEeBzwNE13N3tEA84g3kcHzr0CsNRDA_Qyk85h12rV2abSnTUKmzo3SnamqXFT4LxZZqXGWVPnuG2c2d5N7e-5VrqWpcMr0y2aZYdlvcZqoStPlzjX1rx7l8-t0yHaK7xUH33PIXq6vHgcXwXT28n1-GwaqJBSFkScqoTTQqo0i5hkYaRVAozwOIoKRgvKICUcFMnCIiP-EUIWJyzjPIuJojkbolHvq2zjnNWFaK2ppF0LAmJTk_A1id-aPHDSA610PnZhZa2M-6Fin4gD8TLey1am1Ot_TMX57OHPF0HPGtfpjx9W2jfhsyeReL6ZiPu7eTydwFyk7AsygYkK</recordid><startdate>198810</startdate><enddate>198810</enddate><creator>Horiike, Michio</creator><creator>Hirano, Chisato</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>198810</creationdate><title>Mass spectrometric indication of double bond position in dodecenals without any chemical derivatization</title><author>Horiike, Michio ; Hirano, Chisato</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4223-592c792fac8b53a345ec70319655f32f2308190c1b4fb15ec043673b99b61c2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Mass spectrometry</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horiike, Michio</creatorcontrib><creatorcontrib>Hirano, Chisato</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Biological Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horiike, Michio</au><au>Hirano, Chisato</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mass spectrometric indication of double bond position in dodecenals without any chemical derivatization</atitle><jtitle>Biological Mass Spectrometry</jtitle><addtitle>Biol. Mass Spectrom</addtitle><date>1988-10</date><risdate>1988</risdate><volume>17</volume><issue>4</issue><spage>301</spage><epage>306</epage><pages>301-306</pages><issn>1052-9306</issn><issn>0887-6134</issn><eissn>1096-9888</eissn><eissn>2376-3868</eissn><coden>BEMSEN</coden><abstract>Ten positional isomers (Δ2‐Δ11) of unmodified dodecenal were analysed by conventional combined gas chromatography/electron impact mass spectrometry. The relative abundances of some predominant fragments in the isomers examined varied with the position of the original double bond. Eminent dominance of a particular isomer over the others in their relative intensities was observed at some fragment ion peaks. The intensity ratios of certain selected pairs of predominant fragment ions are of diagnostic value for the identification of the double bond position. A procedure for the characterization of the double bond position in the chain is given.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/bms.1200170413</doi><tpages>6</tpages></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection |
subjects | Chemistry Exact sciences and technology Mass spectrometry Organic chemistry Reactivity and mechanisms |
title | Mass spectrometric indication of double bond position in dodecenals without any chemical derivatization |
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