Journal
DALTON TRANSACTIONS
Volume -, Issue 46, Pages 6628-6633Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b810234a
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Funding
- Deutsche Forschungsgemeinschaft [SFB 424, A16]
- NRW International Graduate School of Chemistry
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The rare-earth metal hydroxylamide compound Y[N(SiHMe2)(2)](2)[ONBn2][THF] (1) was prepared by the silylamide elimination pathway from the reaction of N, N-dibenzylhydroxylamine, Bn2NOH (Bn = CH2C6H5), with Y[ N(SiHMe2)(2)](3)[THF](2) and was characterised by multinuclear NMR spectroscopy and elemental analysis. The compounds [Cp2Y(ONBn2)](2) (2a) [Cp2Sm(ONBn2)](2) (2b) were obtained by the reactions of MCp3 (M = Y, Sm) with Bn2NOH. The trinuclear compound Cp5Y3[ON(Me)CH2CH2(Me)NO](2) (3) was obtained by the reaction of YCp3 and the bishydroxylamine HON(Me)CH2CH2(Me)NOH. 2a, 2b and 3 were characterised by NMR spectroscopy, single-crystal X-ray diffraction and elemental analysis. In all these complexes side-on-coordination of the hydroxylamide units was observed. The compounds are of dynamic nature in solution.
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