Studies in mass spectrometry. III-formation of a common intermediate in the primary fragmentation process of 1-phenylcyclobutene and of 2-phenyl-1,3-butadiene
The mass spectra of the title compounds show peaks corresponding to the primary fragmentation of H, CH3 and (H2 + C2H2). Kinetic study suggests that the molecular ion of 1‐phenylcyclobutene and 2‐phenyl‐1,3‐butadiene loses H and CH3 through formation of a common intermediate. This is confirmed by ap...
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Veröffentlicht in: | Organic Mass Spectrometry 1975-11, Vol.10 (11), p.935-945 |
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description | The mass spectra of the title compounds show peaks corresponding to the primary fragmentation of H, CH3 and (H2 + C2H2). Kinetic study suggests that the molecular ion of 1‐phenylcyclobutene and 2‐phenyl‐1,3‐butadiene loses H and CH3 through formation of a common intermediate. This is confirmed by appearance potential and ionisation potential measurements, fragmentation of deuterium labelled compounds and the corrected Z values. |
doi_str_mv | 10.1002/oms.1210101104 |
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III-formation of a common intermediate in the primary fragmentation process of 1-phenylcyclobutene and of 2-phenyl-1,3-butadiene</title><title>Organic Mass Spectrometry</title><addtitle>Org. Mass Spectrom</addtitle><description>The mass spectra of the title compounds show peaks corresponding to the primary fragmentation of H, CH3 and (H2 + C2H2). Kinetic study suggests that the molecular ion of 1‐phenylcyclobutene and 2‐phenyl‐1,3‐butadiene loses H and CH3 through formation of a common intermediate. 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III-formation of a common intermediate in the primary fragmentation process of 1-phenylcyclobutene and of 2-phenyl-1,3-butadiene</title><author>Derocque, Jean-Luc ; Jochem, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2424-56339dde6a15f3e09d5ffb504e344c7614f94204419e37aa8feaeb6f83e1c8dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Derocque, Jean-Luc</creatorcontrib><creatorcontrib>Jochem, Martin</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Organic Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Derocque, Jean-Luc</au><au>Jochem, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies in mass spectrometry. III-formation of a common intermediate in the primary fragmentation process of 1-phenylcyclobutene and of 2-phenyl-1,3-butadiene</atitle><jtitle>Organic Mass Spectrometry</jtitle><addtitle>Org. Mass Spectrom</addtitle><date>1975-11</date><risdate>1975</risdate><volume>10</volume><issue>11</issue><spage>935</spage><epage>945</epage><pages>935-945</pages><issn>0030-493X</issn><eissn>1096-9888</eissn><abstract>The mass spectra of the title compounds show peaks corresponding to the primary fragmentation of H, CH3 and (H2 + C2H2). Kinetic study suggests that the molecular ion of 1‐phenylcyclobutene and 2‐phenyl‐1,3‐butadiene loses H and CH3 through formation of a common intermediate. This is confirmed by appearance potential and ionisation potential measurements, fragmentation of deuterium labelled compounds and the corrected Z values.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/oms.1210101104</doi><tpages>11</tpages></addata></record> |
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title | Studies in mass spectrometry. III-formation of a common intermediate in the primary fragmentation process of 1-phenylcyclobutene and of 2-phenyl-1,3-butadiene |
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