Issue 8, 1985

Stereospecific synthesis of a metallo-enolate: E-[Zr{OC(SiMe3)[double bond, length half m-dash]CHAr}Cl(η-C5H5)2](structurally characterised)via carbonylation of [Zr{CH(SiMe3)Ar}Cl(η-C5H5)2](Ar = 9-anthryl)

Abstract

Treatment of Li{CH(SiMe3)Ar}(tmeda)(Ar = 9-anthryl, tmeda = Me2N[CH2]2NMe2) with zirconocene(IV) chloride in tetrahydrofuran at 20 °C affords [Zr{CH(SiMe3)Ar}Cl(η-C5H5)2], which rapidly reacts with carbon monoxide (PCO 1 atm, 20 °C) in toluene to afford exclusively the E-metallo-enolate [Zr{OC(SiMe3)[double bond, length half m-dash]CHAr}Cl(η-C5H5)2], having Zr–O 1.950(4)Å and < Zr–O–C 157.7(3)°.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 521-522

Stereospecific synthesis of a metallo-enolate: E-[Zr{OC(SiMe3)[double bond, length half m-dash]CHAr}Cl(η-C5H5)2](structurally characterised)via carbonylation of [Zr{CH(SiMe3)Ar}Cl(η-C5H5)2](Ar = 9-anthryl)

M. F. Lappert, C. L. Raston, L. M. Engelhardt and A. H. White, J. Chem. Soc., Chem. Commun., 1985, 521 DOI: 10.1039/C39850000521

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements