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Bulking up CpBIG: A Penta-Terphenyl Cyclopentadienyl Ligand.


ABSTRACT: The modification of cyclopentadienyl ligands with carefully selected substituents is a widely used strategy for tuning their steric and electronic properties. We describe the synthesis of an extremely bulky penta-terphenyl cyclopentadienyl ligand (CpT5) by arylation of cyclopentadiene. Deprotonation reactions with various group 1 metals and bases afforded a complete series of alkali metal salts MCpT5 (M = Li-Cs). The compounds were isolated as solvate-free salts, which were characterized by multinuclear nuclear magnetic resonance spectroscopy, ultraviolet-visible spectroscopy, and elemental analysis. Single-crystal X-ray diffraction studies of LiCpT5, NaCpT5 (crystallized as a solvate with one tetrahydrofuran molecule per formula unit), and KCpT5 revealed the formation of metallocene-like sandwich structures in the solid state.

SUBMITTER: Hierlmeier G 

PROVIDER: S-EPMC8965875 | biostudies-literature | 2022 Mar

REPOSITORIES: biostudies-literature

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Bulking up Cp<sup>BIG</sup>: A Penta-Terphenyl Cyclopentadienyl Ligand.

Hierlmeier Gabriele G   Wolf Robert R  

Organometallics 20220315 6


The modification of cyclopentadienyl ligands with carefully selected substituents is a widely used strategy for tuning their steric and electronic properties. We describe the synthesis of an extremely bulky penta-terphenyl cyclopentadienyl ligand (Cp<sup>T5</sup>) by arylation of cyclopentadiene. Deprotonation reactions with various group 1 metals and bases afforded a complete series of alkali metal salts MCp<sup>T5</sup> (M = Li-Cs). The compounds were isolated as solvate-free salts, which were  ...[more]

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