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Article Dans Une Revue Chemistry - A European Journal Année : 2019

Toward Transition-Metal-Templated Construction of Arylated B-4 Chains by Dihydroborane Dehydrocoupling

Résumé

The reactivity of a diruthenium tetrahydride complex towards three selected dihydroboranes was investigated. The use of [DurBH ] (Dur=2,3,5,6-Me C H) and [(Me Si) NBH ] led to the formation of bridging borylene complexes of the form [(Cp*RuH) BR] (Cp*=C Me ; 1 a: R=Dur; 1 b: R=N(SiMe ) ) through oxidative addition of the B-H bonds with concomitant hydrogen liberation. Employing the more electron-deficient dihydroborane [3,5-(CF ) -C H BH ] led to the formation of an anionic complex bearing a tetraarylated chain of four boron atoms, namely Li(THF) [(Cp*Ru) B H (3,5-(CF ) C H ) ] (4), through an unusual, incomplete threefold dehydrocoupling process. A comparative theoretical investigation of the bonding in a simplified model of 4 and the analogous complex nido-[1,2(Cp*Ru) (μ-H)B H ] (I) indicates that there appear to be no classical σ-bonds between the boron atoms in complex I, whereas in the case of 4 the B chain better resembles a network of three B-B σ bonds, the central bond being significantly weaker than the other two.

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Chimie organique
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hal-02438529 , version 1 (29-01-2020)

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Carsten Lenczyk, Dipak Kumar Roy, Kai Oberdorf, Joern Nitsch, Rian D. Dewhurst, et al.. Toward Transition-Metal-Templated Construction of Arylated B-4 Chains by Dihydroborane Dehydrocoupling. Chemistry - A European Journal, 2019, 25 (72), pp.16544-16549. ⟨10.1002/chem.201904772⟩. ⟨hal-02438529⟩
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