作者: A. Weisz , A. Mandelbaum , J. Shabanowitz , D. F. Hunt
关键词: Protonation 、 Cis–trans isomerism 、 Spectral line 、 Chemistry 、 Collision-induced dissociation 、 Double bond 、 Stereospecificity 、 Mass spectrometry 、 Medicinal chemistry 、 Stereochemistry 、 Ion 、 Instrumentation (computer programming) 、 Molecular medicine 、 Biochemistry
摘要: Low energy collision induced dissociation (CID) spectra were measured by a triple stage quadrupole mass spectrometer for the [MH]+ ions of diethyl and dimethyl esters maleic, fumaric, citraconic mesaconic acids. A very high degree stereospecificity was observed geometrically isomeric esters. The cis give rise to abundant [MHEtOH]+ [MHEtOHC2H4]+ ions, while trans isomers exhibit [MHC2H4]+ [MH2 C2H4]+ ions. highly stereospecific processes indicate that double bond configuration is retained in protonated species under conditions experiment.