Synthesis of cationic zinc complexes from protonated diazadienes and ZnR2 (R = Et, N(SiMe3)(2)). The crystal structures of Pr(i)DADH H2N{B(C6F5)(3)}(2) , {Pr(i)DADZn( mu-OH)}(2) H2N{B(C6F5)(3)}(2) (2), and Ph*DADZnN(SiMe3)(2) H2N{B(C6F5)(3)}(2)

Hannant, M. D., Schormann, M., Hughes, D. L. and Bochmann, M. (2005) Synthesis of cationic zinc complexes from protonated diazadienes and ZnR2 (R = Et, N(SiMe3)(2)). The crystal structures of Pr(i)DADH H2N{B(C6F5)(3)}(2) , {Pr(i)DADZn( mu-OH)}(2) H2N{B(C6F5)(3)}(2) (2), and Ph*DADZnN(SiMe3)(2) H2N{B(C6F5)(3)}(2). Inorganica Chimica Acta, 358 (5). pp. 1683-1691. ISSN 0020-1693

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Abstract

Protonation of (MeC=NC6H3Pr2i-2,6)(2) (Pr'DAD) with [H(OEt2)(2)][HN{B(C6F5)(3)}(2)] affords the immonium salt [Pri- DADH][H2N{B(C6F5)(3)}(2)] (1) which shows intra- and inter-ionic NH center dot center dot center dot F hydrogen bonding in the solid state. Protolysis of ZnEt2 with [Pr(i)DADH][H2N{B(C6F5)(3)}(2)] gives [(Pr(i)DAD)ZnEt][H2N{B(C6F5)(3)}(2)] as a reactive intermediate. Repeated recrystallizations allowed the isolation of the dimeric zinc hydroxo complex [{(Pr(i)DAD)Zn(mu-OH)}(2)][H2N{(B(C6F5)(3)}(2)](2) (2) which shows asymmetric OH-bridges. The analogous reaction of [Ph*DADH][H2N{B(C6F5)(3)}(2)] [Ph*DAD = (MeC=NC6H3Ph2-2,6)(2) with ZnMe2 or M{N(SiMe3)(2) gives the three-coordinate Zn and Cd compounds [(Ph*DAD)ZnMe][H2N{B(C6F5)(3)}(2)] (5) and [(Ph*DAD)MN(SiMe3)(2)][H2N{B(C6F5)(3)}(2)] (6 M = Zn; 7, M = Cd). The crystal structures of 1, 2 and 6 are reported. (c) 2004 Elsevier B.V. All rights reserved.

Item Type: Article
Faculty \ School: Faculty of Science > School of Chemistry
Depositing User: Rachel Smith
Date Deposited: 16 Jun 2011 13:47
Last Modified: 20 Sep 2020 23:35
URI: https://ueaeprints.uea.ac.uk/id/eprint/32753
DOI: 10.1016/j.ica.2004.11.012

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