Cationic η 3-allyl complexes. 21. Telomerization of buta-1,3-diene with Z–H compounds mediated by group 10 complexes
Identifieur interne : 000D20 ( Main/Exploration ); précédent : 000D19; suivant : 000D21Cationic η 3-allyl complexes. 21. Telomerization of buta-1,3-diene with Z–H compounds mediated by group 10 complexes
Auteurs : Faouzi Bouachir [Tunisie] ; Pierre Grenouillet [France] ; Denis Neibecker [France] ; Jacques Poirier [France] ; Igor Tkatchenko [France]Source :
- Journal of Organometallic Chemistry [ 0022-328X ] ; 1998.
Descripteurs français
- Wicri :
- topic : Platine.
English descriptors
- KwdEn :
Abstract
Cationic (η3-allyl) complexes of general formula [(η3-allyl)M(ligand)2]+Y−, where Y− is a non-coordinating anion (BF4−, ClO4−, BF4−) have been examined in telomerization reactions of buta-1,3-diene with representative nucleophiles. No reaction are observed for nickel complexes, due to their high reactivity versus nucleophiles. With palladium complexes, the reaction only occurs with alcohols and provides an increased selectivity for telomers with more than two diene units, leading to C16, C24 and even higher ethers. Although much less reactive, platinum complexes can also produce higher telomers when hydrogenosilanes are used. It is proposed, at least in the case of palladium, that the formation of C16 and C24 ethers arises from the coupling of C8 units within dimeric palladium intermediates with the telogen acting as a bridging ligand.
Url:
DOI: 10.1016/S0022-328X(98)00789-X
Affiliations:
- France, Tunisie
- Auvergne-Rhône-Alpes, Gouvernorat de Monastir, Midi-Pyrénées, Occitanie (région administrative), Rhône-Alpes
- Monastir, Toulouse, Villeurbanne
- Université de Monastir
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000F76
- to stream Istex, to step Curation: 000B53
- to stream Istex, to step Checkpoint: 000714
- to stream Main, to step Merge: 000D60
- to stream Main, to step Curation: 000D20
Le document en format XML
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<front><div type="abstract" xml:lang="en">Cationic (η3-allyl) complexes of general formula [(η3-allyl)M(ligand)2]+Y−, where Y− is a non-coordinating anion (BF4−, ClO4−, BF4−) have been examined in telomerization reactions of buta-1,3-diene with representative nucleophiles. No reaction are observed for nickel complexes, due to their high reactivity versus nucleophiles. With palladium complexes, the reaction only occurs with alcohols and provides an increased selectivity for telomers with more than two diene units, leading to C16, C24 and even higher ethers. Although much less reactive, platinum complexes can also produce higher telomers when hydrogenosilanes are used. It is proposed, at least in the case of palladium, that the formation of C16 and C24 ethers arises from the coupling of C8 units within dimeric palladium intermediates with the telogen acting as a bridging ligand.</div>
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