(η6-Arene)tricarbonylchromium and (η5-cyclohexadienyl) tricarbonylmanganese complexes: indirect nucleophilic substitutions
✍ Scribed by Françoise Rose-Munch; Vanessa Gagliardini; Christophe Renard; Eric Rose
- Book ID
- 104111786
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 528 KB
- Volume
- 178-180
- Category
- Article
- ISSN
- 0010-8545
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✦ Synopsis
Treatment of X-substituted (g6-arene)tricarbonylchromium complexes with a nucleophile and a proton source afforded new arenetricarbonylchromium complexes via chromium hydride intermediates and elimination of HX (cine and tele nucleophilic aromatic substitutions). Treatment of (g5-X-substituted-cyclohexadienyl )tricarbonyl manganese complexes with hydride and a proton source gave g5-cyclohexadienyl complexes resulting from a cleavage of the C-X bond: the g3-X-substituted cyclohexenyl intermediates underwent elimination of an agostic hydrogen and the X group.
📜 SIMILAR VOLUMES
Addition of a nucleophile to an (η 6 -arene)tricarbonylchromium or a tricarbonyl(η 5 -cyclohexadienyl)manganese complex substituted with a leaving group X (X = F, Cl, OMe, OPh, NR 2 ) affords (after treatment with acid) new complexes with the same η 6 or η 5 hapticity. The overall reaction involves