Abstract:
A new phosphorescent iridium(III) complex,
bis[2′,6′-difluorophenyl-4-formylpyridinato-N,C4′]iridium(III)
(picolinate) (IrC), was synthesized, fully characterized by
various spectroscopic techniques, and utilized for the detection
of CN− on the basis of the widely known hypothesis of the
formation of cyanohydrins. The solid-state structure of the
developed IrC was authenticated by single-crystal X-ray
diffraction. Notably, the iridium(III) complex exhibits intense
red phosphorescence in the solid state at 298 K (ΦPL = 0.16)
and faint emission in acetonitrile solution (ΦPL = 0.02). The
cyanide anion binding properties with IrC in pure and aqueous
acetonitrile solutions were systematically investigated using two
different channels: i.e., by means of UV−vis absorption and
photoluminescence. The addition of 2.0 equiv of cyanide to a
solution of the iridium(III) complex in acetonitrile (c = 20 μM) visibly changes the color from orange to yellow. On the other
hand, the PL intensity of IrC at 480 nm was dramatically enhanced ∼5.36 × 102-fold within 100 s along with a strong signature
of a blue shift of the emission by ∼155 nm with a detection limit of 2.16 × 10−8 M. The cyanohydrin formation mechanism is
further supported by results of a 1H NMR titration of IrC with CN−. As an integral part of this work, phosphorescent test strips
have been constructed by impregnating Whatman filter paper with IrC for the trace detection of CN− in the contact mode,
exhibiting a detection limit at the nanogram level (∼265 ng/mL). Finally, density functional theory (DFT) and time-dependent
density functional theory (TD-DFT) calculations were performed to understand the electronic structure and the corresponding
transitions involved in the designed phosphorescent iridium(III) complex probe and its cyanide adduct
