Issue 5, 2012

Synthesis and characterization of organo-scandium and yttrium complexes stabilized by phosphinoamide ligands

Abstract

Addition of three equivalents of phosphinoamine, (ArNHPiPr2) [Ar = 3,5-dimethylphenyl] to M(CH2SiMe3)3(THF)2 [M = Sc, Y] precursors gives complexes of the form (ArNPiPr2)3M(THF) [M = Sc, Y]. In the case of scandium, addition of Sc(CH2SiMe3)3(THF)2 to (ArNPiPr2)3Sc(THF) affords (ArNPiPr2)2Sc(CH2SiMe3)(THF), which has been isolated and structurally characterized. In contrast, addition of Y(CH2SiMe3)3(THF)2 to (ArNPiPr2)3Y(THF) generates a distribution of phosphinoamide-containing products consistent with the formulations (ArNPiPr2)2Y(CH2SiMe3)(THF) and (ArNPiPr2)Y(CH2SiMe3)2(THF), as ascertained using NMR spectroscopy. Attempts to react the alkyl-containing phosphinoamide complexes with small molecules such as H2 led to disproportionation type processes.

Graphical abstract: Synthesis and characterization of organo-scandium and yttrium complexes stabilized by phosphinoamide ligands

Supplementary files

Article information

Article type
Paper
Submitted
08 Aug 2011
Accepted
31 Oct 2011
First published
06 Dec 2011

Dalton Trans., 2012,41, 1524-1528

Synthesis and characterization of organo-scandium and yttrium complexes stabilized by phosphinoamide ligands

N. R. Halcovitch and M. D. Fryzuk, Dalton Trans., 2012, 41, 1524 DOI: 10.1039/C1DT11501D

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