2007
DOI: 10.1002/rcm.3341
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Fragmentation mechanisms in electron ionization mass spectrometry of 5‐nitro‐ and 8‐nitroquinoline: a comparative study

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Cited by 2 publications
(1 citation statement)
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“…Homolytic cleavage of the S bond produced the radical anions at m / z 192 for bithionol (Table , #1); the heterolytic cleavage of this bond with hydrogen transfer produced the product ion at m / z 161, that lost HCl to produce the product ion at m / z 125 proposed with the benzyne structure. This type of benzyne structure has been reported for the product ions of similar compounds …”
Section: Resultssupporting
confidence: 73%
“…Homolytic cleavage of the S bond produced the radical anions at m / z 192 for bithionol (Table , #1); the heterolytic cleavage of this bond with hydrogen transfer produced the product ion at m / z 161, that lost HCl to produce the product ion at m / z 125 proposed with the benzyne structure. This type of benzyne structure has been reported for the product ions of similar compounds …”
Section: Resultssupporting
confidence: 73%