Sarah L. Stoll, Simon G. Bott and Andrew R. Barron
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)]2
with either Se or Se
PPh3, while both it and
[ButIn(µ-SeBut
)]2 may be
prepared from
[But2In(µ-Cl)]n and
(ButSe)MgCl. Similarly,
[Bun2In(µ-SeBut
)]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
].
Reaction of [But2M(µ-Cl)]n
(M = In or Ga) with
Se(SiMe3
)2 yielded the silylselenolate
compounds
[But2M(µ-SeSiMe3
)]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.