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Reactions of Bis(alkyl)yttrium Complexes Supported by Bulky N,N Ligands with 2,6-Diisopropylaniline and Phenylacetylene

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Reactions_of_Bis_alkyl_yttrium_Complexes_Supported_by_Bulky_N_N_Ligands_with_2_6_Diisopropylaniline_and_Phenylacetylene/2497138
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The reactions of bis­(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands (LY­(CH2SiMe3)2(THF)n: L = Ap, n = 1 (1); L = Amd, n = 1 (2)) with 2,6-diisopropylaniline and phenylacetylene were performed. The reaction of 1 with an equimolar amount of 2,6-diisopropylaniline occurs with TMS elimination and affords an yttrium alkyl anilido species which was isolated as a DME adduct, ApY­(CH2SiMe3)­(NH-2,6-iPr2C6H3)­(DME) (3). The protonolysis of 3 with phenylacetylene results in the alkynyl anilido derivative ApY­(CCPh)­(NH-2,6-iPr2C6H3)­(DME) (6). The treatment of complexes 3 and 6 with 2,2′-bipy leads to the formation of the bis­(anilido) derivative ApY­(NH-2,6-iPr2C6H3)2(bipy) (5). The formation of a dimeric complex containing two ApY fragments linked by two μ2-alkynyl groups and a μ-η2:η2-butatrienediyl fragment, [{AmdY­(μ2-CCPh)}2(μ2-η2:η2-PhCCCCPh)] (7), was observed in the reaction of 2 with 2 equiv of phenylacetylene.
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2016-02-20
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