4.6 Article

From an Easily Accessible Pentacarbonylcobalt(I) Salt to Piano-Stool Cations [(arene)Co(CO)2]

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 23, Issue 58, Pages 14658-14664

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201703589

Keywords

carbonyl ligands; cobalt; density functional calculations; metal carbonyl cation; vibrational spectroscopy; Weakly Coordinating Anion (WCA)

Funding

  1. Albert-Ludwigs-Universitat Freiburg
  2. Deutsche Forschungsgemeinschaft (DFG)
  3. European Research Council (ERC Advanced Grant UniChem)

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The facile synthesis of a pentacarbonyl cobalt(I) salt without the need for a superacid as solvent is presented. This salt, [Co(CO)(5)](+)[Al(ORF)(4)](-) {R-F=C(CF3)(3)}, readily accessible on a multigram scale, undergoes substitution reactions with arenes yielding the hitherto unknown class of two-legged cobalt piano-stool complexes [(arene)Co(CO)(2)](+) with four different arene ligands. Such a substitution chemistry would have been impossible in superacid solution, as the arenes used would have been oxidized and/or protonated. Thus, the general approach described herein may have a wide synthetic use. Additionally, the thermochemistry of the piano-stool complexes is shown to be not easy to describe computationally and most of the established DFT methods overestimate the reaction energies. Only CCSD(T) calculations close to the basis set limit gave energies fully agreeing with the experiment.

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