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Versatile Ln2(μ-NR)2‑Imide Platforms for Ligand Exchange and Isoprene Polymerization

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Figshare2015-12-17 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Versatile_Ln_sub_2_sub_NR_sub_2_sub_Imide_Platforms_for_Ligand_Exchange_and_Isoprene_Polymerization/2054943
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Bimetallic rare-earth-metal imide complexes Ln2(μ2-Ndipp)­(μ3-Ndipp)­[(μ2-Me)2AlMe]­(AlMe4)2 (3-Ln; Ln = Y, La, Ce, Nd; dipp = 2,6-diisopropylphenyl) have been obtained from the reaction of Ln­(AlMe4)3 (1-Ln) with Li­(NHdipp) (2). X-ray diffraction studies of toluene-soluble 3-Ln revealed an unusual Ln­[{(μ2-Me)2AlMe}­(μ3-Ndipp)]­Ln moiety as the most striking feature. Facile salt-metathetical exchange of the tetramethylaluminato ligands in 3-Ln with K­(L) (L = N­(SiMe3)2, Cp′) allowed for the isolation of Ln2(Ndipp)2[N­(SiMe3)2]2(AlMe3) (4-La), partially exchanged Ln2(Ndipp)2(Cp′)­(AlMe4)­(AlMe3) (5-La, Cp′ = C5Me4SiMe3), and Ln2(Ndipp)2(Cp′)2(AlMe3) (6-La). Attempted cleavage of the AlMe3 moiety in 3-Ln with THF led to C–H bond activation of one of the isopropyl methine moieties to produce Ln2(μ2-Ndipp)­[(μ3-NC6H3-2-CMe2-6-iPr)­Al­(μ2-Me)2]­(AlMe4)2 (7-La). Selective cleavage of the bridging AlMe3 “cap” was achieved by addition of DMAP (DMAP = 4-dimethylaminopyridine) to produce [Ln­(μ2-Ndipp)­(AlMe4)­(DMAP)]n (8-Ln; Ln = La, Ce) and concomitantly DMAP·AlMe3. The organoaluminum-free compounds [Ln­(μ2-Ndipp)­{N­(SiMe3)2}­(DMAP)]2 (9-Ln; Ln = La, Ce), [Ln­(μ2-Ndipp)­(Cp′)­(DMAP)]2 (10-La), and [Ln­(μ2-Ndipp)­(OAr)­(DMAP)]2 (11-Ln; Ln = La, Ce; Ar = 2,6-di-tert-butyl-4-methylphenyl) were obtained via reactions of 8-Ln with K­(L) (L = Cp′, N­(SiMe3)2, OAr). In the presence of activators [Ph3C]­[B­(C6F5)4] and [PhNMe2H]­[B­(C6F5)4], AlEt2Cl complexes 3-Ln, 5-Ln, and 7-Ln initiate the polymerization of isoprene to yield PIPs with narrow molecular weight distributions, involving new imido-supported bimetallic catalysts.
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2015-12-17
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