Remote Substituent Effects on Allylic and Benzylic Bond Dissociation Energies. Effects on Stabilization of Parent Molecules and Radicals
✍ Scribed by Zavitsas, Andreas A.; Rogers, Donald W.; Matsunaga, Nikita
- Book ID
- 127088037
- Publisher
- American Chemical Society
- Year
- 2007
- Tongue
- English
- Weight
- 208 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0022-3263
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## Abstract Reactions of isopropyl and of undecyl radicals with __meta‐__ and __para__‐substituted toluenes are reported. The results demonstrate that the reactivities of toluenes are due to both benzyl‐H abstraction and addition of the alkyl radicals to the aromatic ring. Relative reactivities yie
The bond-dissociation energies (BDEs) of more than twenty areneϪM + complexes (M = Cr, Fe, Co) have been studied by mass spectrometry, using the kinetic method. With minor exceptions, the same relative order of BDEs is found for the three metals and the series of substituted arenes: electrondonating