Factors Controlling the Addition of Carbon-Centered Radicals to Alkenes-An Experimental and Theoretical Perspective

• Published in: Angewandte Chemie International Edition 2001-04, Vol.40 (8), p.1340-1371
• Main Authors: Fischer, Hanns, Radom, Leo
• Format: Article
• Language: English
• Subjects: ab initio calculations; additions; kinetics; radical reactions
• ISSN: 1433-7851; 1521-3773
• DOI: 10.1002/1521-3773(20010417)40:8<1340::AID-ANIE1340>3.0.CO;2-#

The successful exploitation of syntheses involving the generation of new carbon–carbon bonds by radical reactions rests on some prior knowledge of the rate constants for the addition of carbon‐centered radicals to alkenes and other unsaturated molecules, and of the factors controlling them. Two former classical reviews in Angewandte Chemie by Tedder (1982) and by Giese (1983) provided mechanistic insight and led to various qualitative rules on the complex interplay of enthalpic, polar, and steric effects. In the meantime, the field has experienced very rapid progress: many more experimental absolute rate constants have become available, and there have been major advances in the efficiency and reliability of quantum‐chemical methods for the accurate calculation of transition structures, reaction barriers, and reaction enthalpies. Herein we review this progress, recommend suitable experimental and theoretical procedures, and display representative data series for radical additions to alkenes. On this basis, and guided by the pictorial tool of the state‐correlation diagram for radical additions, we then offer a new and more stringent quantification of the controlling factors. Our analysis leads to a partial revision of the previous qualitative rules, and it more clearly exhibits the interplay of the reaction enthalpy effects, polar charge‐transfer contributions, and steric substituent effects on the reaction energy barrier. The various contributions are cast into the form of new, simple, and physically meaningful but non‐linear, predictive equations for the preestimation of rate constants. These equations prove successful in several tests but call for additional theoretical and experimental foundation. The kinetics of related reactions such as polymer propagation, copolymerization, and the addition of radicals to alkynes and aromatic compounds is shown to follow the same principles. Better prediction of the rate constants of radical addition to alkenes is possible by using new, simpler, physically more sensible, but nonlinear, equations. Starting from representative, experimentally and theoretically obtained data sets and clear state‐correlation diagrams for radical addition reactions, the controlling factors have been qualified in a new and rigorous manner. The results of this method lead to a partial revision of the existing qualitative rules and show more clearly how the reaction enthalpy, charge transfer, and the steric effects of substituent groups affec