## Abstract DFT computations on the mechanisms of nucleophilic substitutions on benzyl bromides were performed and the calculated activation parameters were compared with experimentally acquired data. In vacuo, the presence of electron‐withdrawing (e‐w) groups on the benzyl bromides accelerated the
✦ LIBER ✦
Molecular structures and reactivity of trifluoromethyltris(dialkylamino)phosphonium bromides
✍ Scribed by Alexander N. Chernega; Alexander A. Kolomeitsev; Yurij L. Yagupolskij; Andreas Gentzsch; Gerd-Volker Röschenthaler
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 408 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-1139
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