TY - JOUR

T1 - Iridium Complexes with BIAN-Type Ligands: Synthesis, Structure and Redox Chemistry

AU - Romashev, Nikolai F.

AU - Bakaev, Ivan V.

AU - Komlyagina, Veronika I.

AU - Abramov, Pavel A.

AU - Mirzaeva, Irina V.

AU - Nadolinny, Vladimir A.

AU - Lavrov, Alexander N.

AU - Kompan’kov, Nikolai B.

AU - Mikhailov, Artem A.

AU - Fomenko, Iakov S.

AU - Novikov, Alexander S.

AU - Sokolov, Maxim N.

AU - Gushchin, Artem L.

PY - 2023/6/21

Y1 - 2023/6/21

N2 - A series of iridium complexes with bis(diisopropylphenyl)iminoacenaphtene (dpp-bian) ligands, [Ir(cod)(dpp-bian)Cl] ( 1), [Ir(cod)(NO)(dpp-bian)](BF 4) 2 ( 2) and [Ir(cod)(dpp-bian)](BF 4) ( 3), were prepared and characterized by spectroscopic techniques, elemental analysis, X-ray diffraction analysis and cyclic voltammetry (CV). The structures of 1- 3 feature a square planar backbone consisting of two C = C π-bonds of 1,5-cyclooctadiene (cod) and two nitrogen atoms of dpp-bian supplemented with a chloride ion (for 1) or a NO group (for 2) to complete a square-pyramidal geometry. In the nitrosyl complex 2, the Ir-N-O group has a bent geometry (the angle is 125°). The CV data for 1 and 3 show two reversible waves between 0 and -1.6 V (vs. Ag/AgCl). Reversible oxidation was also found at E 1/2 = 0.60 V for 1. Magnetochemical measurements for 2 in a range from 1.77 to 300 K revealed an increase in the magnetic moment with increasing temperature up to 1.2 μ B (at 300 K). Nitrosyl complex 2 is unstable in solution and loses its NO group to yield [Ir(cod)(dpp-bian)](BF 4) ( 3). A paramagnetic complex, [Ir(cod)(dpp-bian)](BF 4) 2 ( 4), was also detected in the solution of 2 as a result of its decomposition. The EPR spectrum of 4 in CH 2Cl 2 is described by the spin Hamiltonian Ĥ = gβHŜ with S = 1/2 and g xx = g yy = 2.393 and g zz = 1.88, which are characteristic of the low-spin 5d 7-Ir(II) state. DFT calculations were carried out in order to rationalize the experimental results.

AB - A series of iridium complexes with bis(diisopropylphenyl)iminoacenaphtene (dpp-bian) ligands, [Ir(cod)(dpp-bian)Cl] ( 1), [Ir(cod)(NO)(dpp-bian)](BF 4) 2 ( 2) and [Ir(cod)(dpp-bian)](BF 4) ( 3), were prepared and characterized by spectroscopic techniques, elemental analysis, X-ray diffraction analysis and cyclic voltammetry (CV). The structures of 1- 3 feature a square planar backbone consisting of two C = C π-bonds of 1,5-cyclooctadiene (cod) and two nitrogen atoms of dpp-bian supplemented with a chloride ion (for 1) or a NO group (for 2) to complete a square-pyramidal geometry. In the nitrosyl complex 2, the Ir-N-O group has a bent geometry (the angle is 125°). The CV data for 1 and 3 show two reversible waves between 0 and -1.6 V (vs. Ag/AgCl). Reversible oxidation was also found at E 1/2 = 0.60 V for 1. Magnetochemical measurements for 2 in a range from 1.77 to 300 K revealed an increase in the magnetic moment with increasing temperature up to 1.2 μ B (at 300 K). Nitrosyl complex 2 is unstable in solution and loses its NO group to yield [Ir(cod)(dpp-bian)](BF 4) ( 3). A paramagnetic complex, [Ir(cod)(dpp-bian)](BF 4) 2 ( 4), was also detected in the solution of 2 as a result of its decomposition. The EPR spectrum of 4 in CH 2Cl 2 is described by the spin Hamiltonian Ĥ = gβHŜ with S = 1/2 and g xx = g yy = 2.393 and g zz = 1.88, which are characteristic of the low-spin 5d 7-Ir(II) state. DFT calculations were carried out in order to rationalize the experimental results.

KW - Crystallography, X-Ray

KW - Iridium/chemistry

KW - Ligands

KW - Oxidation-Reduction

KW - Spectrum Analysis

UR - https://www.mendeley.com/catalogue/67022269-ad57-3518-af3f-dd955af71e61/

U2 - 10.3390/ijms241310457

DO - 10.3390/ijms241310457

M3 - Article

C2 - 37445638

VL - 24

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1422-0067

IS - 13

M1 - 10457

ER -