Fragmentation studies of tetrahydropyridocarbazole derivatives by EI, ESI-MS/MS and FAB
2001 ◽
Vol 15
(1)
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pp. 19-25
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Keyword(s):
Four tetrahydropyridocarbazole derivatives were analysed by different mass spectrometry techniques: electrospray ionization, fast atom bombardment and by low and high resolution 70 eV electron ionization. Retro Diels Alder is the main fragmentation pathway, whereas other pathways leading to [M—1]+, [M—CH3]+and double charge ions also occur to considerable extents. Semi-empirical calculation provided some evidence on the nature of tropylium ions [M—1]+. Calculation of ΔHf0indicated that [M+—1] could be formed preferentially when a hydrogen atom is lost from the methyl substituent of the homoaromatic ring.
1992 ◽
Vol 3
(8)
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pp. 842-846
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2002 ◽
pp. 781-786
1992 ◽
Vol 6
(9)
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pp. 547-549
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1990 ◽
Vol 1
(6)
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pp. 455-472
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1993 ◽
Vol 22
(3)
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pp. 170-175
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Keyword(s):
1991 ◽
Vol 538
(2)
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pp. 323-330
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1996 ◽
Vol 79
(4)
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pp. 929-935
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