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Article Dans Une Revue European Journal of Inorganic Chemistry Année : 2013

N-Heterocyclic Carbenes Functioning as Monoligating Clamps

Résumé

Benzimidazolium salts N,N′-disubstituted with 9-alkylfluorenyl groups (3a-e, alkyl = methyl, ethyl, propyl, butyl, benzyl) have been synthesised in high yields in three steps from o-phenylenediamine. This amine was treated with fluorenone in the presence of TiCl4 and tetramethylethylenediamine (TMEDA) to form N,N′-bis(9H-fluoren-9-ylidene)benzene-1,2-diamine (1) in 91 % yield. Diamines 2a-e were then obtained in yields superior or equal to 77 % by reacting diimine 1 with the appropriate organolithium reagent. In the final step, diamines 2a-e were treated with ethylorthoformate under acidic conditions to afford benzimidazolium salts 3a-e. These were readily converted into the PEPPSI palladium complexes 4a-e (PEPPSI = pyridine-enhanced precatalyst preparation stabilisation and initiation). NMR and X-ray diffraction studies revealed that the flat fluorenylidene moiety orientates the alkyl groups towards the metal centre and because of its restricted rotational freedom makes the ligand bulkiness time independent. Thus, the metal centre is permanently confined between the two alkyl groups, and thereby forms a monoligating clamp with the carbenic centre. The CH2 groups close to the palladium ion give rise to anagostic C-H***Pd interactions. Catalytic tests revealed that the palladium complexes 4a-e are highly efficient in Suzuki-Miyaura cross-coupling reactions; their activity is equal or superior to the best PEPPSI catalysts reported to date.

Dates et versions

hal-00854496 , version 1 (27-08-2013)

Identifiants

Citer

Matthieu Teci, Eric Brenner, Dominique Matt, Loïc Toupet. N-Heterocyclic Carbenes Functioning as Monoligating Clamps. European Journal of Inorganic Chemistry, 2013, 2013 (16), pp.2841-2848. ⟨10.1002/ejic.201300087⟩. ⟨hal-00854496⟩
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