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

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
<mark>Journal publication date</mark>7/02/2012
<mark>Journal</mark>Dalton Transactions
Issue number5
Volume41
Number of pages5
Pages (from-to)1524-1528
Publication StatusPublished
Early online date6/12/11
<mark>Original language</mark>English

Abstract

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