The dication
[(cymene)Ru(η6-1-Me-indoline)]2+,
1a, has been synthesized either by the
hydrogenation of [(cymene)Ru(1-Me-indole)]2+
or by the reaction of
[(cymene)Ru(OTf)2]
x
with
1-Me-indoline and has been isolated as the triflate or
tetraphenylborate salt. Other [(arene)Ru(indoline)]2+ derivatives have also been prepared
by similar methods.
[1a](BPh4)2
crystallized in the space group P1̄ with a
= 10.9308(3) Å, b = 14.1874(4) Å,
c = 18.4139(5)
Å, α = 81.800(1)°, β = 75.17°, γ = 89.50°,
V = 2731.19(13) Å3, and Z =
2. The sandwich
structure is slightly bent with an angle between the ruthenium ion and
the center of each
η6-ligand of 174.3°. Complexes with
η1-N-coordinated indoline ligands have also
been
characterized. The reaction of indoline with
Pd(Cl)2(PPh3)(CH3CN)
in refluxing dichloromethane resulted in the formation of
(Cl)2(PPh3)Pd(η1-indoline),
2, which was isolated and
characterized by spectroscopic methods. Complex 2
crystallized in the space group P1̄ with
a = 9.703(2) Å, b = 10.148(2) Å,
c = 13.920(2) Å, α = 99.650(10)°, β =
99.230(10)°, γ =
94.560(10)°, V = 1325.8(3) Å3,
and Z = 2. The indoline ligand is tilted with respect
to the
metal−ligand plane, and the five-membered ring of the ligand assumes
an envelope-type
conformation.