Download PDF
Synlett 1996; 1996(2): 111-118
DOI: 10.1055/s-1996-5338
account
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Unusual Reactions of Titanocene- and Zirconocene-Generating Complexes

A. Ohff, S. Pulst, C. Lefeber, N. Peulecke, P. Arndt, V. V. Burkalov, U. Rosenthal*
  • *Max-Planck-Gesellschaft, Arbeitsgruppe ”Komplexkatalyse” an der Universität Rostock, Buchbinderstr. 5-6, 18055 Rostock, Germany, Phone +49 381 4669376; Fax +49 381 4669386; E-mail UROSEN@chemie1.Uni-Rostock.DE
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

The titanocene alkyne complex without any additional ligands Cp2Ti(Me3SiC≡CSiMe3) 1 and the zirconocene alkyne complexes free from stabilizing phosphine ligands (Cp2Zr(L)(Me3SiC≡CSiMe3) (L = THF 2, pyridine 3) as well as the metallacyclic complex Cp2Zr-O-CMe2-C(SiMe3)=C(SiMe3) 4 react with some substrates in an unusual manner depending on metals M, ligands L and the substituents R of the substrates. Also in some cases the competitive reaction of coupling of the complexed alkyne occurs. In this account all products without coupling of the silylalkyne are numbered, the data of detailed NMR studies and X-ray crystal structure analyses are given in the cited references.

The reaction of ”Cp2Zr” with benzophenone gives the ligand stabilized metallocene η2-ketone complex 5. With di(tert-butyl)acetylene-dicarboxylate a coupling of a C≡C- and a C=O-ester group to 6 and with bis(trimethylsilyl)acetylenedicarboxylate an unusual 1,3-migration of a SiMe3 unit from an oxygen to a carbon atom yielding the dimeric complex 7 occurs.

Ketimines react with metallocenes either to the ligand stabilized η2-complexes 8 or the derivatives bearing N-H functions to amido alkylideneamido complexes 9 and 10 by a hydrogen transfer reaction. Aldimines give the cyclic diamido complex 11 or in the case of a methyl group at the nitrogen under evolution of methane an unsaturated cyclic complex. Heterocyclic C=N systems, e.g. benzoxazoles or benzthiazoles, show a ring enlargement and a simultaneous coupling to 12 and 13 or, e.g. benzisoxazoles, yield without coupling the dimeric complex 14.

Depending on metals, ligands, substituents and used stoichiometry the generated metallocenes ”Cp2M” react with one equivalent of 1,4-disubstituted 1,3-butadiynes RC≡C-C≡CR’ to give five-membered metallacyclic cumulenes 15 and 16 or with a half equivalent of the diyne the bimetallic complexes 17-19. Two diyne molecules are coupled by ”Cp2Ti” to yield a titanacyclopentadiene 20 in contrast to ”Cp2Zr”, which gives the seven-membered zirconacyclic cumulenes 21 and 22.

Titanocene - zirconocene - alkyne complexes - butadiynes - coupling reactions - metallacyclocumulenes - C-C and Si-H bond activations

      >