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Phosphido- and Amidozirconocene Cation-Based Frustrated Lewis Pair Chemistry

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NIAID Data Ecosystem2026-03-08 收录
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https://figshare.com/articles/dataset/Phosphido_and_Amidozirconocene_Cation_Based_Frustrated_Lewis_Pair_Chemistry/2201041
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资源简介:
Methyl abstraction from neutral [Cp2ZrMe­(ERR′)] complexes 1 (E = N, P; R, R′ = alkyl, aryl) with either B­(C6F5)3 or [Ph3C]­[B­(C6F5)4] results in the formation of [Cp2Zr­(ERR′)]­[X] complexes 2 (X– = MeB­(C6F5)3–, B­(C6F5)4–). The X-ray structure of amido complexes [Cp2Zr­(NPh2)]­[MeB­(C6F5)3] (2d) and [Cp2Zr­(NtBuAr)]­[B­(C6F5)4] (2e′, Ar = 3,5-C6H3(CH3)2) is reported, showing a sterically dependent Zr/N−π interaction. Complexes 2 catalyze the hydrogenation of electron-rich olefins and alkynes under mild conditions (room temperature, 1.5 bar H2). Complex 2e binds CO2, giving [Cp2Zr­(CO2)­(NtBuAr)]2[MeB­(C6F5)3]2 (3e). Amido complex 2d reacts with benzaldehyde yielding [Cp2Zr­(OCH2Ph)­((OC)­PhNPh2)]­[MeB­(C6F5)3] (7d). Phosphido complex [Cp2Zr­(PCy2)]­[MeB­(C6F5)3] (2a) reacts with diphenylacetylene to yield frustrated Lewis pair [Cp2Zr­(PhCCPh)­(PCy2)]­[MeB­(C6F5)3] (8a) which further reacts with a range of carbonyl substrates.
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2016-02-15
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