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Journal ArticleDOI

Pentaphosphaferrocene als Komplexliganden

Otto J. Scherer, +2 more
- 01 Nov 1989 - 
- Vol. 122, Iss: 11, pp 2049-2054
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TLDR
In this article, the 30-VE triple-decker complexes [CpFe(μ, η5-P5)Fe(C5Me4R)] and PF6 (3a, R = CH3; 3b: R = C2H5; Cp = C5-C5H5) were characterized by X-ray structure analyses.
Abstract
Die Umsetzung von [Cp*Fe(P5)] (1a) mit [Cr(CO)5(THF)] bzw. [Cp(CO)2Mn(THF)] ergibt [Cp*Fe(P5){Cr(CO)5}2] (2) sowie [HCp*Fe(P5){Mn(CO)2Cp}n] (4a–d; 1–4; Cp* = η5-C5Me5). Aus 1 und [CpFe(C6H6)]PF6 lassen sich photochemisch die kationischen 30-VE-Tripeldeckerkomplexe [CpFe(μ, η5-P5)Fe(C5Me4R)]PF6 (3a: R = CH3; 3b: R = C2H5; Cp = η5-C5H5) aufbauen. Zusatzlich zu den NMR-spektroskopischen Studien wurden von 2 und 3b Kristallstrukturanalysen angefertigt. Pentaphospaferrocenes as Complex Ligands The interaction of [Cp*Fe(P5)] (1a) with [Cr(CO)5(thf)] and [Cp(CO)2Mn(thf)], respectively, affords [Cp*Fe(P5){Cr(CO)5}2] (2) as well as [Cp*Fe(P5){Mn(CO)2Cp}n] (4a–d; n = 1–4; Cp* = η5-C5Me5). Irradiation of 1 and [CpFe(C6H6)]PF6 gives the cationic 30-VE triple-decker complexes [CpFe(μ, η5-P5)Fe(C5Me4R)]PF6 (3a: R = CH3; 3b: R = C2H5; Cp = η5-C5H5). In addition to the NMR studies 2 and 3b have been characterized by X-ray structure analyses.

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Citations
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Journal ArticleDOI

P4 Activation by Late-Transition Metal Complexes†‡

TL;DR: The coordination chemistry of white phosphorus is nowadays a mature discipline, which during the last four decades has reached a deep understanding of the mechanisms governing the metal-mediated activation of this unique and highly reactive molecule.
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The chemistry of phospha- and polyphosphacyclopentadienide anions

TL;DR: The synthesis, structural and spectroscopic features, organic and coordination chemistry of phospholide and polyphospholide anions are comprehensively reviewed in this article, where the synthesis and coordination of anions is discussed.
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Komplexe mit substituentenfreien acyclischen und cyclischen Phosphor‐, Arsen‐, Antimon‐ und Bismutliganden

TL;DR: In this paper, ausschlieslich Verbindungen wie R3E, R2E(CH2NER2)nER2 and RC[(CH 2NER 2]3 (E = P,As,Sb,Bi), deren freies Elektronenpaar am E-Atom als 2e-Donor fungiert, deren E4-Liganden auf, denen man sowohl in Form intakter Tetraeder als auch als Bestandteile
Journal ArticleDOI

Pentaphosphaferrocene as a Linking Unit for the Formation of One‐ and Two‐Dimensional Polymers

TL;DR: In this paper, a cyclo-P5-ligand complex with copper halide and copper product reacts with CuBr and CuI to give two-dimensional networks in which 1 is the linking unit.
References
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Book ChapterDOI

Structural and Bonding Patterns in Cluster Chemistry

TL;DR: In this paper, the borane-carborane structural pattern has been studied in a wide range of other compounds, including metal clusters, metal-hydrocarbon 7∼ complexes, and various neutral or charged hydrocarbons.
Journal ArticleDOI

Synthesis of the first 30-electron triple-decker complexes of the iron group metals with cyclopentadienyl ligands. X-Ray structure of [(η-C5H5)Ru(μ,η-C5Me5) Ru(η-C5Me5)]PF6

TL;DR: The first 30-electron triple-decker complexes of the iron group metals were synthesized by reaction of [Fe(η-C5H5)Ru(μ,η -C5Me5)M′(θ-C 5Me5)]PF6 in this article, where the pentamethylcyclopentadienyl ligand is the middle deck in these sandwich compounds.
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