TRANSITION STRUCTURES FOR CONJUGATE AND CARBONYL ADDITIONS OF CYANIDE TO S-CIS-ACROLEIN AND S-TRANS-ACROLEIN - AN ABINITIO MO STUDY

被引：33

作者：

WONG, SS

PADDONROW, MN

LI, Y

HOUK, KN

机构：

[1] UNIV NEW S WALES,DEPT ORGAN CHEM,POB 1,KENSINGTON,NSW 2033,AUSTRALIA

[2] UNIV CALIF LOS ANGELES,DEPT CHEM & BIOCHEM,LOS ANGELES,CA 90024

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1990年 / 112卷 / 24期

关键词：

D O I：

10.1021/ja00180a007

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Transition structures for the addition of cyanide anion to s-cis-and s-trans-acrolein and to ethylene and formaldehydehave been located with ab initio MO calculations with use of the 3-21G and 6-31+G* basis sets. Energies of all stationarypoints, including reactants, ion-dipole complexes, and products, were evaluated at the second-order MØller-Plesset correlation level with the 6-31+G* basis set. The relative reaction barriers for conjugate and carbonyl additions are discussed for gas-phase and solution-phase reactions. Calculations predict that, in the gas phase, the reaction barrier for conjugate addition to s-cis-acrolein is slightly higher than that for carbonyl addition, whereas the reverse situation is found for addition to s-trans-acrolein. The conjugate addition products are also more stable than the carbonyl addition products. The reaction barrier for carbonyl addition is expected to become smaller than that for conjugate addition in solution, under which conditions the difference in the stabilities of the conjugate and carbonyl products should become relatively small. © 1990, American Chemical Society. All rights reserved.

引用

页码：8679 / 8686

页数：8

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