Advances in the chemistry of bis-cyclopentadienyl hydride derivatives of niobium and tantalum

Citation
A. Antinolo et al., Advances in the chemistry of bis-cyclopentadienyl hydride derivatives of niobium and tantalum, COORD CH RE, 195, 1999, pp. 43-72
Citations number
134
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
COORDINATION CHEMISTRY REVIEWS
ISSN journal
00108545 → ACNP
Volume
195
Year of publication
1999
Pages
43 - 72
Database
ISI
SICI code
0010-8545(199910)195:<43:AITCOB>2.0.ZU;2-V
Abstract
The bis-cyclopentadienyl hydride chemistry of the elements niobium and tant alum has been dominated by the family of trihydride complexes, namely Cp2MH 3 (M = Nb, Ta, Cp=C5H5, C5Me5, C5H4SiMe3, C5H3(SiMe3)(2) and related substi tuted cyclopentadienyl rings). The chemical and spectroscopic properties of these complexes are strongly influenced by both the nature of the Cp ring and the metal center. In some cases, anomalous NMR spectroscopic behavior h as been observed, and values of J(HH) that are largely dependent on the tem perature have been found. This behavior can be modulated by means of the in teraction of the trihydride complexes with Group 11 metal fragments, and in some cases HH interactions in the molecules can be observed. Several X-ray crystal structure determinations of this kind of complex, as well as diffe rent theoretical calculations, have been performed in order to gain a deepe r insight into these systems. The reactivity of the trihydride metallocene complexes has been extensively considered. Thus, the easy elimination of H- 2 from the Cp2MH3 species, giving rise to the unsaturated species Cp2MH3 ha s been used to study the activation processes of several kinds of H-X bend, in hydrosilanes, hydrogermananes, etc., which allows the synthesis of comp lexes such as Cp2MH2X. This type of complex has been extensively studied, e specially when X = SiR3, because in several cases these complexes exhibit a special hypervalence behavior. A large family of complexes of stoichiometr y Cp2MHL was prepared from the reaction of the Cp2MH3, complexes with diffe rent classes of pi-acid ligands, L. The Cp2MHL complexes can undergo insert ion reactions into the M-H bond with several classes of unsaturated molecul es, and such processes are of interest in the field of organic synthesis. F urthermore, the protonation processes of the Cp2MHL complexes give rise to a new family of eta(2)-H-2-containing cationic species, Cp2M(eta(2)-H-2)L+, which are stable at low temperatures. The NMR data of such compounds indic ate that it is possible to block the rotation of the H-2 molecule at low te mperatures. Of particular interest are the Cp2MH(olefin) complexes, and the se have been widely studied because they can be considered as excellent mod els for the study of the beta-elimination reaction and the reverse olefin i nsertion process. Finally, from the trihydride derivatives Cp2MH3 and relat ed species, several heterometallic complexes have been prepared and charact erized. (C) 1999 Elsevier Science S.A. All rights reserved.