Synthesis, characterization, and reactivity of scandium chloro, alkyl, aryl, and borohydride complexes, Sc(eta(5)-C5H5)R[N((SiMe2CH2PPr2)-Pr-i)(2)] (R = Cl, Me, Ph, and BH4)

Citation
Md. Fryzuk et al., Synthesis, characterization, and reactivity of scandium chloro, alkyl, aryl, and borohydride complexes, Sc(eta(5)-C5H5)R[N((SiMe2CH2PPr2)-Pr-i)(2)] (R = Cl, Me, Ph, and BH4), CAN J CHEM, 78(7), 2000, pp. 1003-1012
Citations number
44
Categorie Soggetti
Chemistry
Journal title
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE
ISSN journal
00084042 → ACNP
Volume
78
Issue
7
Year of publication
2000
Pages
1003 - 1012
Database
ISI
SICI code
0008-4042(200007)78:7<1003:SCAROS>2.0.ZU;2-3
Abstract
Reaction of ScCl2(THF)[N((SiMe2CH2PPr2)-Pr-i)(2)] with NaCp(DME) leads to S c(eta(5)-C5H5)Cl[N((SiMe2CH2PPr2)-Pr-i)(2)] (1). The X-ray crystal structur e shows the scandium centre to reside in a square pyramidal environment wit h the [N((SiMe2CH2PPr2)-Pr-i)(2)] - ligand bound in a pseudo-meridional fas hion. The H-1 NMR spectrum is consistent with a C-s symmetric structure in solution. Metathesis of the chloride ligand with RLi (R = Me, Ph, BH4) yiel ds the five-coordinate species Sc(eta(5)-C5H5)R[N((SiMe2CH2PPr2)-Pr-i)(2)]. Phenyl 3 and borohydride 4 are isolated as crystalline solids, while methy l 2 resisted crystallization. 2-4 exhibit H-1 NMR spectra consistent with C -s symmetric solution structures. Sc(eta(5)-C5H5)Ph[N((SiMe2CH2PPr2)-Pr-i)( 2)] (3) was characterized in the solid state and found to have a similar ge ometry to that of the parent chloride. Reaction of Sc(eta(5)-C5H5)Me[N((SiM e2CH2PPr2)-Pr-i)(2)] (2) with NH2R (R = Ph, Bu-t) yields the amides Sc(eta( 5)-C5H5)NHPh[N((SiMe2CH2PPr2)-Pr-i)(2)] (5) and Sc(eta(5)-C5H5)(NHBu)-Bu-t- [N((SiMe2CH2PPr2)-Pr-i)(2)] (6) via sigma-bond metathesis routes; these re actions are accompanied by a competing reaction at the scandium-amide bond to produce the protonated ligand, HN((SiMe2CH2PPr2)-Pr-i)(2) 5 and 6 are al so produced by salt-elimination from the chloride 1 and LiNHR (R = Ph, Bu-t ). Sc(eta(5)-C5H5)(BH4)[N((SiMe2CH2PPr2)-Pr-i)(2)] (4) reacts with PMe3 to produce the putative hydride, Sc(eta(5)-C5H5)H[N((SiMe2CH2PPr2)-Pr-i)(2)] ( 7); this species was identified in solution. An equilibrium between 4, PMe3 , 7, and PMe3,BH3 exists which greatly favors the starting scandium-borohyd ride. Crystals of Sc(eta(5)-C5H5)Cl[N((SiMe2CH2PPr2)-Pr-i)(2)] (1) are mono clinic, a = 17.409(2), b = 10.0803(7), c = 17.688(2) A, beta = 94.606(8) de grees, Z = 4, space group P2(1)/c; and those of Sc(eta(5)-C5H5)Ph[N((SiMe2C H2PPr2)-Pr-i)(2)] (3) are triclinic, a = 10.5129(15), b = 19.124(2), c = 9. 114(2) A, alpha = 95.582(13), beta = 107.047(12), gamma = 90.042(11)degrees , Z = 2, space group P. The structures were solved by Patterson (1) and dir ect (3) methods and refined by full-matrix least-squares procedures to R = 0.047 and 0.054 (R-w = 0.042 and 0.049) for 2414 and 2844 reflections with I greater than or equal to 3 sigma(I), respectively.