Inorganic Ferrocene Analogue [Fe(P-4)2](2-)

Wang, Zi-Chuan and Qiao, Lei and Sun, Zhong-Ming and Scheer, Manfred (2022) Inorganic Ferrocene Analogue [Fe(P-4)2](2-). JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 144 (15). pp. 6698-6702. ISSN 0002-7863, 1520-5126

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Abstract

Inorganic metallocene derivatives containing only cyclo-P-n ligands have been targeted for more than 20 years, but their syntheses have never been achieved by pursuing the conventional route of using P-4 phosphorus except for the generation of [Ti(eta(5)-P-5)(2)](2-). Herein, we report a facile one-step method for the synthesis of the homoleptic iron complex [Fe(P-4)(2)](2-) by the Zintl-phase-type precursor KP. P-31 NMR analyses indicate that upon dissolving the KP phase in ethylenediamine P-4(2-) was generated only in the presence of 2,2,2-crypt. The amounts of cation-sequestering agents, the type of iron precursor, and their consuming ratio have a decisive impact on the yield of [Fe(P-4)(2)](2-). Both the FeII and the FeIII precursors can oxidize P-4(2-) to give a concomitant product [(P-7)Fe(P-4)](3-), which can be partially inhibited by the addition of potassium to produce relatively pure crystalline [K(2,2,2-crypt)](2)[Fe(P-4)(2)].

Item Type: Article
Uncontrolled Keywords: HALF-SANDWICH COMPLEXES; PENTAPHOSPHACYCLOPENTADIENIDE ION; CHEMICAL-BOND; SODIUM PENTAPHOSPHACYCLOPENTADIENIDE; CHEMISTRY; PHOSPHORUS; IRON; ANTIAROMATICITY; POLYPHOSPHIDES; AROMATICITY
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Manfred Scheer
Depositing User: Dr. Gernot Deinzer
Date Deposited: 16 Feb 2024 08:47
Last Modified: 16 Feb 2024 08:47
URI: https://pred.uni-regensburg.de/id/eprint/58023

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