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   <subfield code="u">Department of Chemistry, College of Education, University of Basrah, Basrah, Iraq</subfield>
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   <subfield code="a">The mass spectral fragmentation of copper(II) complexes of cyclic β-diketones</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Suhaila Hamdi]</subfield>
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   <subfield code="a">Massenspektroskopische Fragmentierung von Kupfer(II)-Komplexen cyclischer β-Diketone</subfield>
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   <subfield code="a">Summary: Electron impact mass spectra of several bis(2-trifluoroacetylcycloalkanonato) copper(II) and bis(2-acetylcycloalkanonato) copper(II) chelates, in which the cyclic β-diketonate moiety comprises five-, six-, seven-, and eight-membered ring systems, have been recorded. Compared with other copper(II) chelates of acyclic β-diketonates, the present series of copper(II) cyclic β-diketonates exhibited more pronounced intramolecular reduction reactions accompanied by a remarkably facile hydrogen migration resulting in the formation of the [LCu(I)-H]+ ion as the base peak in all complexes investigated. The proposed fragmentation pathways leading to the formation of a number of important copper-containing daughter ions have been confirmed by metastable scanning of the corresponding parent ion spectra using the defocusing technique.</subfield>
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   <subfield code="a">Mass Spectra</subfield>
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   <subfield code="a">Bis(2-trifluoroacetylcycloalkanonato) copper(II)</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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