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Abstract

Antimony-carbon bonds are readily formed by the reaction between an antimony halide and a reactive organometallic compound, such as a Grignard [341], organolithium [342], or organoaluminium [343] reagent, e.g.:

$$ 3PhLi + SbC{l_3} \to P{h_3}Sb + 3LiCl $$
$$ 6MeMgI + 2SbC{l_3} \to 2M{e_3}Sb + 3MgC{l_2} + 3Mg{I_2} $$
$$ 3E{t_3}Al + Sb{F_3} \to E{t_3}Sb + 3E{t_2}AlF $$

Aluminium reagents can also be used to alkylate the oxide, Sb2O3 [17]:

$$ S{b_2}{O_3} + 2{R_3}Al \rightleftharpoons {\left( {{R_2}Sb} \right)_2}O + 2RAlO\overset{{{R_3}Al}}{\rightleftharpoons} 2{R_3}Sb + 3RAlO $$

Alternatively, a bimetallic reagent such as NaAlR3OR′ can be electrolysed using an antimony anode [344].

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© 1979 B. J. Aylett

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Aylett, B.J. (1979). Antimony. In: Organometallic Compounds. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-5729-9_8

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  • DOI: https://doi.org/10.1007/978-94-009-5729-9_8

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-009-5731-2

  • Online ISBN: 978-94-009-5729-9

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