Preparation and structural study of monocyclopentadienylalkoxoniobium (V) derivates. Crystal structure of {[Nb(η-5-C5H4SiMe3)Cl]2(μ-O)(μ-OOC6H4)2}
Authors
Jalón Sotés, Félix Ángel; Otero Montero, Antonio; Royo Gracia, Pascual; Fernández G., Juan M.; Rosales, María J.; [et al.]Identifiers
Permanent link (URI): http://hdl.handle.net/10017/4935DOI: 10.1016/S0022-328X(00)98921-6
ISSN: 0022-328X
Publisher
Elsevier
Date
1987Bibliographic citation
Journal of Organometallic Chemistry, 1987, v.331, n.1, p.C1-C4
Keywords
Alcoholysis
Crystal structure
Niobium
Project
407-84 (Ministerio de Educación y Ciencia)
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Publisher's version
http://dx.doi.org/10.1016/S0022-328X(00)98921-6Rights
© Elsevier, 1987
Access rights
info:eu-repo/semantics/openAccess
Abstract
Alcoholysis with catechol or substitution reactions with NaOPh on Nb(¿5-C5H4R)Cl4 (R = H, SiMe3) have given new alkoxoniobium(V) derivatives of the type Nb(η5-C5H4R)Cl3(OPh) (R = H, SiMe3) Nb(η5-C6H5)Cl2(O2C6H4) and {[Nb(η5-C5H4SiMe3)Cl]2(μ-O)(μ-O2C6H4)2}. The crystal structure of the last species has been studied. The two metal atoms, 3.079(1) Å apart, are symmetrically bridged by the oxo and the two catechol ligands. The two oxygen atoms of each catecholate group are coordinated to the metal atoms, one of them to one Nb atom and the other bridging the two Nb atoms. Chloride and CpSiMe3 ligands complete the coordination sphere of both metal atoms.
Collections
- QUIMINOR - Artículos [236]