The symmetry of the Ion formed by stepwise loss of CO molecules in the mass spectra of p-benzoquinones
Contrary to previous suppositions, it appears that the produced by the loss of 2 CO from para‐benzoquinones passes through the symmetry of not a substituted cyclobutadiene, but rather a substituted tetrahedrane, at least for inert R. The p‐fluoro labeling technique is used to obtain this result.
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Veröffentlicht in: | Organic Mass Spectrometry 1968-08, Vol.1 (4), p.537-542 |
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container_title | Organic Mass Spectrometry |
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creator | Elwood, Thomas A. Bursey, Maurice M. |
description | Contrary to previous suppositions, it appears that the produced by the loss of 2 CO from para‐benzoquinones passes through the symmetry of not a substituted cyclobutadiene, but rather a substituted tetrahedrane, at least for inert R. The p‐fluoro labeling technique is used to obtain this result. |
doi_str_mv | 10.1002/oms.1210010407 |
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Mass Spectrom</addtitle><date>1968-08</date><risdate>1968</risdate><volume>1</volume><issue>4</issue><spage>537</spage><epage>542</epage><pages>537-542</pages><issn>0030-493X</issn><eissn>1096-9888</eissn><abstract>Contrary to previous suppositions, it appears that the produced by the loss of 2 CO from para‐benzoquinones passes through the symmetry of not a substituted cyclobutadiene, but rather a substituted tetrahedrane, at least for inert R. The p‐fluoro labeling technique is used to obtain this result.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/oms.1210010407</doi><tpages>6</tpages></addata></record> |
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title | The symmetry of the Ion formed by stepwise loss of CO molecules in the mass spectra of p-benzoquinones |
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