期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 22, 期 49, 页码 17646-17656出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201602906
关键词
cooperative effects; guanidines; homogeneous catalysis; magnesiates; s-block metals
资金
- University of Strathclyde
- European Research Council
- Spanish Ministerio de Economia y Competitividad (MINECO) [CTQ2014-51912-REDC]
- Junta de Comunidades de Castilla-La Mancha [PEII-2014-041-P]
To advance the catalytic applications of s-block mixed-metal complexes, sodium magnesiate [NaMg(CH2SiMe3)(3)] (1) is reported as an efficient precatalyst for the guanylation of a variety of anilines and secondary amines with carbodiimides. First examples of hydrophosphination of carbodiimides by using a Mg catalyst are also described. The catalytic ability of the mixed-metal system is much greater than that of its homometallic components [NaCH2SiMe3] and [Mg(CH2SiMe3)(2)]. Stoichiometric studies suggest that magnesiate amido and guanidinate complexes are intermediates in these catalytic routes. Reactivity and kinetic studies imply that these guanylation reactions occur via (tris)amide intermediates that react with carbodiiimides in insertion steps. The rate law for the guanylation of N,N'-diisopropylcarbodiimide with 4-tert-butylaniline catalyzed by 1 is first order with respect to [amine], [carbodiimide], and [catalyst], and the reaction shows a large kinetic isotopic effect, which is consistent with an amine-assisted rate-determining carbodiimide insertion transition state. Studies to assess the effect of sodium in these transformations denote a secondary role with little involvement in the catalytic cycle.
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