Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

A family of scandium and yttrium tris((trimethylsilyl)methyl) complexes with neutral N-3 donor ligands

Tredget, Cara S, Lawrence, Sally C., Ward, Benjamin David, Howe, Robert G., Cowley, Andrew R. and Mountford, Philip 2005. A family of scandium and yttrium tris((trimethylsilyl)methyl) complexes with neutral N-3 donor ligands. Organometallics 24 (13) , pp. 3136-3148. 10.1021/om050209r

Full text not available from this repository.

Abstract

The first group 3 organometallic compounds containing the tris(3,5-dimethylpyrazolyl)methane (HC(Me2pz)3) and 1,3,5-trimethyltriazacyclohexane (Me3[6]aneN3) ligands are reported, together with the homologous 1,4,7-triazacyclononane-supported compounds and trichloride derivatives for many of the ligands. Reaction of M(CH2SiMe3)3(THF)2 (M = Sc, Y) with Me3[9]aneN3 (1,4,7-trimethyltriazacyclononane), HC(Me2pz)3, or Me3[6]aneN3 gave the corresponding tris((trimethylsilyl)methyl) derivatives M(Me3[9]aneN3)(CH2SiMe3)3 (M = Sc (1), Y (2)), M{HC(Me2pz)3}(CH2SiMe3)3 (M = Sc (3), Y (4)), and M(Me3[6]aneN3)(CH2SiMe3)3 (M = Sc (12), Y (13)). Reaction of 3 with 2,6-dimethylphenol (ArOH) gave the tris(aryloxide) derivative Sc{HC(Me2pz)3}(OAr)3 (9), and reaction of HC(Me2pz)3 with MCl3 gave M{HC(Me2pz)3}Cl3 (M = Sc (5), Y(6)). Attempts to prepare tris((trimethylsilyl)methyl) complexes with the more sterically demanding tris(3-R-pyrazolyl)methanes (R = iPr, Ph, tBu) or the related tris(pyrazolyl)methylsilane ligand were unsuccessful. However, the trichlorides M{HC(iPrpz)3}Cl3 (M = Sc (7), Y (8)) and M{MeSi(Me2pz)3}Cl3 (M = Sc (10), Y (11)) could be made. In related studies the reaction of ScCl3(THF)3 with Me3[6]aneN3 afforded Sc(Me3[6]aneN3)Cl3 (14), but the yttrium congener could not be prepared. The compounds 1, 3, 4, 9, 11, and 14 have been crystallographically characterized. Competitive ligand exchange reactions for the tris(alkyl) compounds M(L)(CH2SiMe3)3 established the binding preference L = Me3[9]aneN3 > Me3[6]aneN3 > HC(Me2pz)3 for M = Sc and L = Me3[9]aneN3 > HC(Me2pz)3 > Me3[6]aneN3 for M = Y. Reaction of ScR3(THF)2 (R = CH2SiMe3, Ph) with 1-(3,5-di-tert-butyl-2-hydroxybenzyl)-4,7-dimethyltriazacyclononane (HL1) or 1-(3,5-di-tert-butyl-2-hydroxybenzyl)-4,7-diisopropyltriazacyclononane (HL2) gave organoscandium derivatives of mono(phenoxy)-substituted triazacyclononane ligands, namely Sc(L1)R2 (R = CH2SiMe3 (15), Ph (17)) and Sc(L2)(CH2SiMe3)2 (16). Reaction of 15 with 2 equiv of TolOH (Tol = p-tolyl) afforded Sc(L1)(OTol)2 (18), which was crystallographically characterized.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Subjects: Q Science > QD Chemistry
Publisher: American Chemical Society
ISSN: 0276-7333
Last Modified: 04 Jun 2017 02:08
URI: http://orca.cf.ac.uk/id/eprint/9719

Citation Data

Cited 56 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item