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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 : 000D21

Cationic 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 :

RBID : ISTEX:5A5970512B88EB4750B3C3617FD2760F21915950

Descripteurs français

English descriptors

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:


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