<p>Halogenation of heterobimetallic triple-decker complexes containing an E-5 middle deck (E = P, As)</p>

Garbagnati, Anna and Seidl, Michael and Piesch, Martin and Balazs, Gabor and Scheer, Manfred (2022) <p>Halogenation of heterobimetallic triple-decker complexes containing an E-5 middle deck (E = P, As)</p>. POLYHEDRON, 221: 115854. ISSN 0277-5387, 1873-3719

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Abstract

The halogenation of the heterobimetallic triple-decker complexes [(Cp*Fe)(Cp ''' Co)(mu,eta(5):eta(4)-E-5)] (E = P (1), As (6), Cp* = eta(5)-C5Me5, Cp ''' = 1,2,4-tri(tert-butyl)cyclopentadienyl) was investigated. Compound 1 has been oxidised to the isostructural ionic compounds [(Cp*Fe)(Cp ''' Co)(mu-PX)(mu,eta(2):eta(1):eta(1)-P4X4)][Y] (X = I, Y = [I3] (2), X = Br, Y = [FeBr4] (3)) and to the neutral species [(Cp*Fe)(Cp ''' Co)(mu-PCl2)(mu,eta(2):eta(1):eta 1-P4Cl4)] (4) and [(Cp*Fe) (Cp ''' Co)(mu-PCl2)(2)(mu,eta(1):eta(1)-P2Cl3)] (5). Compounds 2, 3 and 4 possess a heterobimetallic nortricyclane-like FeCoP(5 )core. The oxidation of the heavier homologue 6 with bromine and iodine afforded the homometallic complexes [(Cp ''' Co)(2)(mu,eta(4):eta(4)-As4X)][FeX4] (X = I (7) and X = Br (9)). With iodine as halogenating agent, the trinuclear monocation bearing an As6 prism as ligand [(Cp*Fe)(Cp ''' Co)(2)(mu(3),eta(4):eta(4):eta(4)-As-6)][FeI4] (8) was additionally isolated. When PCl5 was used as oxidizing agent, the initially folded As5 ligand planarised resulting in the dicationic species [(Cp*Fe)(Cp ''' Co)(mu,eta(5):eta(5)-As-5)][FeCl4](2) (10).

Item Type: Article
Uncontrolled Keywords: REACTIVITY; PHOSPHORUS; Halogenation; Polyphosphorus complexes; Polyarsenic complexes; Triple-decker complexes
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: 07 Nov 2023 10:03
Last Modified: 07 Nov 2023 10:03
URI: https://pred.uni-regensburg.de/id/eprint/56661

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