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Amine alpha cleavage

Amines Hardly detectable in case of acyclic aliphatic amines high intensity for aromatic and cyclic amines Beta cleavage yielding >C=Nv base peak for all 1° amines at m/e = 30 (CH2=N+H j moderate M-1 peak for aromatic amines loss of 27 (HCN) in aromatic amines fragmentation at alpha carbons in cyclic amines... [Pg.188]

Much like alcohols, amines are also observed to undergo alpha cleavage to generate a resonance-... [Pg.704]

Amines Bearing alpha-CH Bonds. Perhaps the most widely studied family of photogenerated radical cations which suffer C-H bond cleavage within the radical ion pair are the amines. Before addressing the question of deprotonation, we briefly digress to consider the impressive photoactivity of amines as electron transfer sensitizers. [Pg.274]

Thus the halogens preferentially cause the loss of the radical X through a cleavage of the adjacent bond, whereas the amines preferentially lose a radical through a cleavage of the alpha bond. [Pg.284]


See other pages where Amine alpha cleavage is mentioned: [Pg.267]    [Pg.275]    [Pg.280]    [Pg.684]    [Pg.795]    [Pg.340]    [Pg.271]    [Pg.311]    [Pg.60]    [Pg.516]    [Pg.136]    [Pg.1408]    [Pg.85]    [Pg.247]    [Pg.460]    [Pg.319]    [Pg.351]    [Pg.11]    [Pg.38]    [Pg.4716]    [Pg.263]   
See also in sourсe #XX -- [ Pg.374 ]




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