Energy profiles for the identity-reaction
carbon-to-carbon proton transfers from carbon acids of
the type ZCH3 to their conjugate bases
ZCH2
- have been studied by ab
initio methods. Gas-phase
acidities of ZCH3 species are reproduced well at
MP2/6-31+G*//MP2/6-31+G*. The barriers to
proton transfer relative to the separated reactants
(ΔH
TS) in kcal mol-1 are F
(2.2), Cl (−4.2), Br
(−8.2), OH (−2.1), SH (−5.7), SeH (−11.0) at
MP2/6-31+G*//MP2/6-31+G*. Values at MP4/6-31+G**//MP2/6-31+G* are very similar. The orders of acidities
and barrier heights suggest that
the polarizability of Z is the dominant effect on both. That two
or more ion−dipole complexes of
similar energy exist for each system implies that the complexes will be
fluxional. It is doubtful
that these proton transfers could be observed experimentally. The
dominant process for HYCH2
-
+ CH3YH would almost certainly be the transfer of the YH
proton, and calculations on the SN2
reactions ZCH2
- + CH3Z →
ZCH2CH3 + Z- (Z = F, Cl, Br)
reveal them to be strongly exothermic
with barriers 6−10 kcal mol-1 below those for the
corresponding proton transfer processes.
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