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Polycyclic aromatics proton affinities

We turn to the chemical behavior of cycloalkane holes. Several classes of reactions were observed for these holes (1) fast irreversible electron-transfer reactions with solutes that have low adiabatic IPs (ionization potentials) and vertical IPs (such as polycyclic aromatic molecules) (2) slow reversible electron-transfer reactions with solutes that have low adiabatic and high vertical IPs (3) fast proton-transfer reactions (4) slow proton-transfer reactions that occur through the formation of metastable complexes and (5) very slow reactions with high-IP, low-PA (proton affinity) solutes. [Pg.323]

Vandiver, V.J. Leasme, C.S. Eiceman, G.A. Proton affinity equilibria for polycyclic aromatic hydrocarbons at atmospheric pressure in ion mobility spectrometry. Int. J. Mass Spectrom. Ion Processes 1985, 66(2), 223—238. [Pg.413]


See other pages where Polycyclic aromatics proton affinities is mentioned: [Pg.5]    [Pg.660]    [Pg.648]    [Pg.260]    [Pg.260]    [Pg.260]    [Pg.9]    [Pg.31]    [Pg.392]    [Pg.295]    [Pg.147]   
See also in sourсe #XX -- [ Pg.99 , Pg.295 ]




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