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Synthesis and Structure of Aminopyridinato-Stabilized Yttrium and Lanthanum Amides and Their Reactivity towards Alkylaluminium Compounds

✍ Scribed by Christian Döring; Rhett Kempe


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
373 KB
Volume
2009
Category
Article
ISSN
1434-1948

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✦ Synopsis


Abstract

A series of aminopyridinato‐stabilized (amido)lanthanide complexes has been synthesized and characterized. The bulky aminopyridines (2,6‐diisopropylphenyl)[6‐(2,4,6‐triisopropylphenyl)pyridin‐2‐yl]amine (1a) and 6‐(2,4,6‐triisopropylphenyl)pyridin‐2‐ylamine (1b) were introduced by amine elimination reaction with [Ln{N(SiHMe~2~)~2~}~3~(thf)~2~] (Ln = Y, La, thf = tetrahydrofuran, Me = methyl) to obtain the corresponding mono(aminopyridinato) complexes. Single‐crystal X‐ray analyses were carried out for the yttrium derivatives. The complexes are not able to undergo coordinative chain transfer polymerization with ethylene in the presence of alkylaluminium compounds as the corresponding dialkyl complexes do. Investigations of the reactions of the lanthanide aminopyridinato complexes with triethylaluminium or diisobutylaluminium hydride reveal a fast transfer of the aminopyridinato ligand to the aluminium atom. The products of this transfer reaction are aminopyridinato‐stabilized dialkylaluminium compounds. One example of these aluminium complexes was characterized by X‐ray crystal structure analysis. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)


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