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We report on the reactivity of a boryloxy-functionalized phosphaalkyne, [B]OCP ([B] = N,N′-bis(2,6-diisopropylphenyl)-2,3-dihydro-1H-1,3,2-diazaboryl), toward a series of tungsten(0) reagents to afford the novel complex W(η2-PCO[B])3(CO). As with related organometallic complexes… Click to show full abstract
We report on the reactivity of a boryloxy-functionalized phosphaalkyne, [B]OCP ([B] = N,N′-bis(2,6-diisopropylphenyl)-2,3-dihydro-1H-1,3,2-diazaboryl), toward a series of tungsten(0) reagents to afford the novel complex W(η2-PCO[B])3(CO). As with related organometallic complexes of alkynes, the C3v symmetry adopted by this complex imposes that, of the three coordinated phosphaalkyne ligands, two act as four-electron donors while the remaining species donates two electrons to the tungsten metal center. W(η2-PCO[B])3(CO) readily loses carbon monoxide in the presence of Lewis bases to afford W(η2-PCO[B])3(L) (where L = PMe3, CNtBu).
Journal Title: Organometallics
Year Published: 2019
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