By
pursuing the strategy of manipulating natural compounds to obtain
functional materials, in this work, we report on the synthesis and
characterization of a luminescent cationic iridium complex (
cis
-
1
), designed starting from the catecholic
neurotransmitter dopamine, exhibiting the unusual cis arrangement
of the C
∧
N ligands. Through an integrated experimental
and theoretical approach, it was possible to delineate the optoelectronic
properties of
cis
-
1
. In detail, (a)
a series of absorption maxima in the range 300–400 nm was assigned
to metal-to-ligand charge transfer and weak and broad absorption maxima
at longer wavelengths (400–500 nm) were ascribable to spin-forbidden
transitions with a mixed character; (b) there was an intense red phosphorescence
with emission set in the range 580–710 nm; and (c) a highest
occupied molecular orbital was mainly localized on the metal and the
2-phenylpiridine ligand and a lowest unoccupied molecular orbital
was localized on the N
∧
N ligand, with a Δ
H–L
set at 2.20 eV. This investigation allowed the design
of light-emitting electrochemical cell (LEEC) devices endowed with
good performance. The poor literature reporting on the use of
cis
-iridium(III) complexes in LEECs prompted us to investigate
the role played by the selected cathode and the thickness of the emitting
layer, as well as the doping effect exerted by ionic liquids on the
performance of the devices. All the devices exhibited a deep red emission,
in some cases, quite near the pure color (devices #1, #4, and #8),
expanding the panorama of the iridium-based red-to-near-infrared LEEC
devices. The characteristics of the devices, such as the brightness
reaching values of 162 cd/m
2
for device #7, suggested that
the performances of
cis
-
1
are comparable
to those of trans isomers, opening new perspective toward designing
a new set of luminescent materials for optoelectronic devices.