TY - JOUR
T1 - A molecular orbital study of protonation. 5. Equilibrium structures and energies of ions R2COH+
AU - Del Bene, Janet E.
AU - Radovick, Sally
PY - 1978
Y1 - 1978
N2 - Ab initio SCF calculations have been performed to determine the relative proton affinities of the carbonyl bases R2CO and the structures of the ions R2COH+, with R one of the isoelectronic saturated groups CH3, NH2, OH, and F. The predicted order of proton affinity with respect to R is NH2 > CH3 > OH > H > F, which is the same order predicted for the monosubstituted carbonyl bases RCHO. Replacement of the hydrogen atom in RCHO by a second R group causes a further change in the proton affinity of the base in the same direction as observed upon substitution of the first R group, although the effect of two substituents is less than additive except in F2CO. Protonation of carbonyl bases leads to an increase in the C-O bond distance and a decrease in the bond distance between the carbonyl carbon and the substituent, the magnitude of which depends on the substituent. Protonation also causes changes in the bond angles about the carbonyl carbon which are essentially independent of the nature of the substituent, but strongly dependent on the position of the proton relative to the two substituents. Changes in bond lengths and bond angles and in the electron distribution upon protonation of the bases R2CO are similar to the changes which occur upon protonation of the bases RCHO. From the computed results, a model for the protonation of carbonyl bases is proposed.
AB - Ab initio SCF calculations have been performed to determine the relative proton affinities of the carbonyl bases R2CO and the structures of the ions R2COH+, with R one of the isoelectronic saturated groups CH3, NH2, OH, and F. The predicted order of proton affinity with respect to R is NH2 > CH3 > OH > H > F, which is the same order predicted for the monosubstituted carbonyl bases RCHO. Replacement of the hydrogen atom in RCHO by a second R group causes a further change in the proton affinity of the base in the same direction as observed upon substitution of the first R group, although the effect of two substituents is less than additive except in F2CO. Protonation of carbonyl bases leads to an increase in the C-O bond distance and a decrease in the bond distance between the carbonyl carbon and the substituent, the magnitude of which depends on the substituent. Protonation also causes changes in the bond angles about the carbonyl carbon which are essentially independent of the nature of the substituent, but strongly dependent on the position of the proton relative to the two substituents. Changes in bond lengths and bond angles and in the electron distribution upon protonation of the bases R2CO are similar to the changes which occur upon protonation of the bases RCHO. From the computed results, a model for the protonation of carbonyl bases is proposed.
UR - http://www.scopus.com/inward/record.url?scp=0041174139&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0041174139&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0041174139
SN - 0002-7863
VL - 100
SP - 6936
EP - 6941
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 22
ER -