期刊
DALTON TRANSACTIONS
卷 48, 期 45, 页码 16936-16942出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9dt03976g
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资金
- University of St Andrews
- EPSRC [EP/N509759/1]
- EPSRC [1795521] Funding Source: UKRI
Ligand exchange reactions between combinations of the complexes [{((Ar)nacnac)Mg}(2)], where Ar = 2,6-iPr(2)C(6)H(3) (Dip), 2,6-Et2C6H3 (Dep), 2,4,6-Me4C6H2 (Mes), and 2,6-Me2C6H3 (Xyl), [({Ph2P(NDip)(2)}Mg)(2)], [((Ar)nacnac)Li], where Ar = Mes or Xyl, and [{Ph2P(NDip)(2)}Li] were studied in deuterated aromatic and aliphatic solvents, and tetrahydrofuran. The reactions afforded product mixtures with asymmetrically substituted dimagnesium(i) complexes [((Ar)nacnac)MgMg((Ar ')nacnac)], where Ar, Ar ' = Dip, Dep, Mes, Xyl and [{Ph2P(NDip)(2)}MgMg((Ar)nacnac)], where Ar = Mes or Xyl, and suggest that the exchange of anionic ligands on the Mg-2(2+) ion proceeds via an associative mechanism and is strongly dependent on ligand sterics and ligand shape, and can be very rapid. The activation reaction of fullerene C-60 by dimagnesium(i) complexes [{((Ar)nacnac)Mg}(2)] and [({Ph2P(NDip)(2)}Mg)(2)] to fulleride complexes is similarly dependent on ligand sterics and ligand shape, but likely does not involve direct coordination of the fullerene to the Mg centre in dimagnesium(i) compounds prior to its reduction. The new C-60(6-) fulleride complex [({Ph2P(NDip)(2)}Mg)(6)C-60] was prepared, and spectroscopically and structurally characterised.
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