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Hydrotris methimazolyl borate

Submitted by LUIS FERNANDO SOARES and ROSAUCE MENDONCA SILVA Checked by JASON SMEE and MARCETTA DARENSBOURG  [Pg.199]

Departamento de Qmmica, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brasil. [Pg.199]

Reglinski et al. reacted methiamazole with NaBH4, following the same procedure that was reported by Trofimenko to prepare the Tp ligand, obtaining the Tm ligand  [Pg.200]

The synthesis described below for the Tm ligand is based on Trofimenko s literature reports of trispyrazolyl borate and the trismethimazole borate synthesis of Lobbia et al., with modifications in temperature and solvent washes. Hydrogen evolution is monitored at a lower temperature, starting around 100°C. In this way we obtain very pure Tm in better yields. [Pg.200]


L6pez-G6mez MJ, Connelly NG, Haddow MF, Hamilton A, Orpen AG. Huxional rhodium scorpionate complexes of the hydrotris(methimazolyl)borate (Tm) ligand and their static boratrane derivatives. Dalton Trans. 2010 39 5221-5230. [Pg.255]


See other pages where Hydrotris methimazolyl borate is mentioned: [Pg.323]    [Pg.323]    [Pg.199]    [Pg.199]    [Pg.200]    [Pg.201]    [Pg.221]    [Pg.323]    [Pg.323]    [Pg.199]    [Pg.199]    [Pg.200]    [Pg.201]    [Pg.221]    [Pg.6]   


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