Electron ionization mass spectra of naphthoxazine, naphthpyrrolooxazinone and naphthoxazinobenzoxazine derivatives

Olli Martiskainen, F. Fülöp, I. Szatmári, Kalevi Pihlaja

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Some naphthoxazinobenzoxazines (1a, 1b, 2a-2d, 3a, 3b), naphthoxazines (4a, 4b, 5, 6a, 6b) and naphthpyrrolo-oxazinones (7, 8a, 8b) were studied using mass spectrometry to find out regioisomeric effects and the effects of substituents. As expected the spectra of regioisomeric pairs la-3a vs lb-3b were very different. For example the relative abundances of molecular ions were higher for la-3a and the [M - OH]+ ions were observed only for them. Compounds derived from (1-α-aminobenzyl)-2-naphthol were usually characterized by abundant m/z 231 ions and l-aminomethyl-2-naphthol derivatives by m/z 156 ions. Ions related or similar to their complementary ions were also observed. Many of the studied compounds exhibited fairly abundant ions [M - C17H 11O2]+ (1a, 2a, 3a: [M - 247]+), [M - C17H11O2]+· (2b-2d: [M - 232]+·) or ion [M - C17H11O 2]+· (1b, 5, 6a, 7: [M - 156]+). The results may be useful when making regiochemical conclusions.

Original languageEnglish
Pages (from-to)115-129
Number of pages15
JournalArkivoc
Volume2009
Issue number3
Publication statusPublished - 2009

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Ionization
Ions
Derivatives
Electrons
Mass spectrometry

Keywords

  • Electron ionization mass spectrometry
  • Fragmentation pathways
  • Fused heterocyclic compounds
  • Regioisomers

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Electron ionization mass spectra of naphthoxazine, naphthpyrrolooxazinone and naphthoxazinobenzoxazine derivatives. / Martiskainen, Olli; Fülöp, F.; Szatmári, I.; Pihlaja, Kalevi.

In: Arkivoc, Vol. 2009, No. 3, 2009, p. 115-129.

Research output: Contribution to journalArticle

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T1 - Electron ionization mass spectra of naphthoxazine, naphthpyrrolooxazinone and naphthoxazinobenzoxazine derivatives

AU - Martiskainen, Olli

AU - Fülöp, F.

AU - Szatmári, I.

AU - Pihlaja, Kalevi

PY - 2009

Y1 - 2009

N2 - Some naphthoxazinobenzoxazines (1a, 1b, 2a-2d, 3a, 3b), naphthoxazines (4a, 4b, 5, 6a, 6b) and naphthpyrrolo-oxazinones (7, 8a, 8b) were studied using mass spectrometry to find out regioisomeric effects and the effects of substituents. As expected the spectra of regioisomeric pairs la-3a vs lb-3b were very different. For example the relative abundances of molecular ions were higher for la-3a and the [M - OH]+ ions were observed only for them. Compounds derived from (1-α-aminobenzyl)-2-naphthol were usually characterized by abundant m/z 231 ions and l-aminomethyl-2-naphthol derivatives by m/z 156 ions. Ions related or similar to their complementary ions were also observed. Many of the studied compounds exhibited fairly abundant ions [M - C17H 11O2]+ (1a, 2a, 3a: [M - 247]+), [M - C17H11O2]+· (2b-2d: [M - 232]+·) or ion [M - C17H11O 2]+· (1b, 5, 6a, 7: [M - 156]+). The results may be useful when making regiochemical conclusions.

AB - Some naphthoxazinobenzoxazines (1a, 1b, 2a-2d, 3a, 3b), naphthoxazines (4a, 4b, 5, 6a, 6b) and naphthpyrrolo-oxazinones (7, 8a, 8b) were studied using mass spectrometry to find out regioisomeric effects and the effects of substituents. As expected the spectra of regioisomeric pairs la-3a vs lb-3b were very different. For example the relative abundances of molecular ions were higher for la-3a and the [M - OH]+ ions were observed only for them. Compounds derived from (1-α-aminobenzyl)-2-naphthol were usually characterized by abundant m/z 231 ions and l-aminomethyl-2-naphthol derivatives by m/z 156 ions. Ions related or similar to their complementary ions were also observed. Many of the studied compounds exhibited fairly abundant ions [M - C17H 11O2]+ (1a, 2a, 3a: [M - 247]+), [M - C17H11O2]+· (2b-2d: [M - 232]+·) or ion [M - C17H11O 2]+· (1b, 5, 6a, 7: [M - 156]+). The results may be useful when making regiochemical conclusions.

KW - Electron ionization mass spectrometry

KW - Fragmentation pathways

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KW - Regioisomers

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