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Journal ArticleDOI

(1‐Alken)(trimethylphosphan)zirconocen‐Komplexe: Darstellung, Charakterisierung und Reaktivität

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TLDR
The reaction of Zirconocendichloride with 1-alkylmagnesium halide in the presence of trimethylphosphine at room temperature was studied in this paper, showing that this compound is an ideal starting material for synthezising other (alkene)- or (alkyne)zirconocene complexes.
Abstract
Die Reaktion des Zirconocendichlorids mit zwei Aquivalenten n-Butyllithium und Trimethylphosphan liefert (1-Buten)(trimethylphosphan)zirconocen (1) in 83 proz. Ausbeute. Komplex 1 ist ein ausgezeichnetes Ausgansmaterial zur Darstellung weiterer (Alken)- oder (Alkin)zirconocen-Komplexe; so erhalt man durch Verdrangung des 1-Butens mit Ethylen, Styrol oder Tolan die Zirconocen-Komplexe 2, 3 oder 7 in hohen Ausbeuten. Eine weitere Darstellungsmethode fur (1-Alken)(trimethylphosphan)zirconocen-Komplexe ist die Umsetzung von Zirconocendichlorid mit 1-Alkylmagnesiumhalogeniden in Gegenwart von Trimethylphosphan bei Raumtemperatur; z. B. sind so der 1-Propen-Komplex 9 und der 1-Penten-Komplex 10 gut zuganglich. Spektroskopische Untersuchungen (1H-, 13C- und 31P-NMR) zeigen, das alle dargestellten (1-Alken)(trimethylphosphan)zirconocen-Komplexe in Losung bei 0°C als getrennt beobachtbare Rotamerenpaare 1a, b, 3a, b, 9a, b und 10a, b im Verhaltnis ca. 4:1 vorliegen. Die Strukturen des Ethylen-Komplexes 2 und des Styrol-Komplexes 3a wurden zusatzlich durch Kristallstrukturanalysen ermittelt. 1-Alkene)trimethylphosphine)zirconocenes: Preparation, Characterization, and Reactivity (1-Butene)(trimethylphosphine)zirconocene (1) is prepared in 83% yield by subsequent reaction of zirconocene dichloride with two equivalents of n-butyllithium and trimethylphosphine. Reaction of complex 1 with other alkenes or alkynes, e.g. ethylene, styrene, or tolane indicates that this compound is an ideal starting material for synthezising other (alkene)- or (alkyne)zirconocene complexes, e.g. 2, 3, or 7. Another route to (1-alkene)(trimethylphosphine)zirconocenes, e.g. the 1-propene complex 9 or the 1-pentene complex 10, is the reaction of zirconocene dichloride with 1-alkylmagnesium halide in the presence of trimethylphosphine at room temperature. Spectroscopic investigations 1H-, 13C-, and 31P-NMR spectroscopy) confirm that in solution, complex 1 as well as the other 1-alkene complexes 3, 9, and 10 exist as a mixture of two rotamers 1a, b, 3a, b, 9a, b, and 10a, b in a ca. 4:1 ratio. The structures of the ethylene complex 2 and the styrene complex 3a are also determined by X-ray analyses.

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Journal ArticleDOI

Patterns of Stoichiometric and Catalytic Reactions of Organozirconium and Related Complexes of Synthetic Interest

TL;DR: In this paper, the reactions of organometallic zirconium compounds are reviewed and a specific interest is placed on reactions where C-C bonds are formed, where the authors focus on the reactions where the C-c bond is formed.
Journal ArticleDOI

Titanium and Zirconium Complexes That Contain the Tridentate Diamido Ligands [(i-PrN-o-C6H4)2O]2- ([i-PrNON]2-) and [(C6H11N-o-C6H4)2O]2- ([CyNON]2-)

TL;DR: A variety of five-and six-coordinate titanium and zirconium dialkyl complexes that contain the [(i-PrN-o-C6H4)2O]2-) ligand have been prepared as discussed by the authors.
Journal ArticleDOI

Alkene and Alkyne Complexes of Zirconocene. Their Preparation, Structure, and Novel Transformations.

TL;DR: In this paper, the properties of Cp2Zr(n-Bu)2, CpZrEt2, and Cp 2Zr (t-Bu)(i-Bu), as well as their structures are reviewed.
Journal ArticleDOI

Struktur, Eigenschaften und NMR-spektroskopische Charakterisierung von Cp2Zr(Pyridin)(Me3SiCCSiMe3)†

TL;DR: In this paper, the substitution of THF ligand in Cp2Zr(pyridine) with pyridine yields Cp 2 Zr(η1-NC5H5)(Me3SiCCSiMe3) (3).
References
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Book

Orbital Interactions in Chemistry

TL;DR: In this article, the authors introduce the concept of molecular orbitals of Diatomic Molecules and Electronegativity Perturbation, and propose a method to construct a molecular orbital construction from fragments of small building blocks.
Journal ArticleDOI

Reaction of zirconocene dichloride with alkyllithiums or alkyl grignard reagents as a convenient method for generating a “zirconocene” equivalant and its use in zirconium-promoted cyclization of alkenes, alkynes, dienes, enynes, and diynes☆

TL;DR: In this paper, the treatment of Cl2ZrCp2 with 2 equiv of alkylmetals (RM) containing Li or Mg, e.g., n-BuLi, in THF produces organozirconium species that act as sources of ZrC p2, the latter product being a convenient reagent for preparing zirconacycles.
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