Selenide and selenolate compounds of indium: a comparative study of In–Se bond-forming reactions

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Sarah L. Stoll, Simon G. Bott and Andrew R. Barron


Abstract

A range of In–Se bond-forming reactions have been investigated, including insertion of selenium into either an In–C or In–S bond, reaction of an indium halide with a magnesium selenolate and via chlorosilane elimination. The reaction of InBut3 with Se yielded [But2In(µ-SeBut)]2 and [ButIn(µ3-Se)]4. In contrast, In(CMe2Et)3 and InBun3 with Se preferentially formed [(Me2EtC)In(µ3-Se)]4 and [BunIn(µ3-Se)]4, respectively. The reaction of In(CMe2Et)3 with Te yielded [(Me2EtC)In(µ3-Te)]4]. The compound [ButIn(µ3-Se)]4 is also formed from the reaction of [But2In(µ-SBut[hair space])]2 with either Se or Se[double bond, length as m-dash]PPh3, while both it and [ButIn(µ-SeBut[hair space])]2 may be prepared from [But2In(µ-Cl)]n and (ButSe)MgCl. Similarly, [Bun2In(µ-SeBut[hair space])]2 may be prepared from [Bun2In(µ-Cl)]2. However, the reaction of [(Me2EtC)2In(µ-Cl)]2 with (ButE)MgCl (E = S, Se or Te) yielded [(Me2EtC)In(µ3-E)4[hair space]]. Reaction of [But2M(µ-Cl)]n (M = In or Ga) with Se(SiMe3[hair space])2 yielded the silylselenolate compounds [But2M(µ-SeSiMe3[hair space])]2 . The various In–Se bond-forming reactions are compared. The molecular structures of [But2In(µ-EBut)]2 (E = S or Se) have been determined by X-ray crystallography.


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