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Donor-dictated interlocking co-complexation reactions of LiNHDipp with dimethylzinc: synthesis and structures of new methyl(amido)zincates

Clegg, W. and Graham, D.V. and Herd, E. and Hevia, E. and Kennedy, A.R. and McCall, M.D. and Russo, L. (2009) Donor-dictated interlocking co-complexation reactions of LiNHDipp with dimethylzinc: synthesis and structures of new methyl(amido)zincates. Inorganic Chemistry, 48 (12). pp. 5320-5327. ISSN 0020-1669

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Abstract

A systematic study of the interlocking co-complexation reactions between the primary lithium amide LiNHDipp (Dipp = 2,6-diisopropylphenyl) and dimethylzinc in the presence of different donor ligands is presented which concludes that the final outcome of these reactions is largely dictated by the type of structure that is formed when the donor is coordinated to the lithium amide. When chelating diamine TMEDA (N,N,N',N'-tetramethylethylenediamine) is employed [{Li(2)(NHDipp)(2)(TMEDA)}(infinity)] (1) is obtained, where Li(2)N(2) rings are connected by TMEDA bridges generating a polymeric chain arrangement which does not form a co-complex with Me(2)Zn even in the presence of an excess of TMEDA. The tridentate ligand PMDETA (N,N,N',N'',N''-pentamethyldiethylenetriamine) when reacted with LiNHDipp forms monomeric [(PMDETA)Li(NHDipp)](4) which successfully forms a mixed-metal co-complex with Me(2)Zn affording dialkyl(amido)zincate [(PMDETA)LiZn(NHDipp)(Me)(2)] (2). When the co-complexation reaction is carried out in the presence of monodentate tetrahydrofuran (THF), zincate [(THF)(3)LiZn(NHDipp)(Me)(2)] (3) is obtained which was found to partially decompose in hexane solution after long periods of time at room temperature (2 weeks) to afford the unprecedented "zinc-rich" zincate [(THF)(3)LiZn(2)(Me)(3)(NHDipp)(2)] (5). This compound presents a unique structure in the solid state previously unknown in organozincate chemistry with a trinuclear Li...Zn...Zn chain arrangement where the metals are connected by only two amido bridges and therefore both zinc centers exhibit trigonal planar geometries. 5 can be prepared in good yields by the rational reaction of LiNHDipp with a 2:1:3 mixture of Me(2)Zn, NH(2)Dipp and THF. The different solid-state structural motifs of compounds 1, 2, 4, and 5 have been revealed by X-ray crystallographic studies. Multinuclear NMR ((1)H, (13)C and (7)Li) spectroscopic data recorded in C(6)D(6) solution are also reported for compounds 1-6. Mixed-metal compounds 2 and 5 constitute the first examples of crystallographically characterized alkyl(amido)zincates containing a primary amide.

Item type: Article
ID code: 16947
Keywords: interlocking co-complexation reactions, LiNHDipp, donor ligands, lithium amide, polymeric chain arrangement, organozincate chemistry, Chemistry, Physical and Theoretical Chemistry, Inorganic Chemistry
Subjects: Science > Chemistry
Department: Faculty of Science > Pure and Applied Chemistry
Related URLs:
    Depositing user: Strathprints Administrator
    Date Deposited: 05 May 2010 14:18
    Last modified: 05 Sep 2014 03:30
    URI: http://strathprints.strath.ac.uk/id/eprint/16947

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