Research output: Contribution to journal › Article › peer-review
Effect of the donor–acceptor properties of ligands on the spectroscopic and electrochemical properties of mixed-ligand complexes of Pt(II) and Ir(III) with cyclometalated 2-phenylbenzothiazole. / Katlenok, E. A.; Smirnov, S. N.; Ivanov, A. Yu; Makarenko, S. V.; Balashev, K. P.
In: Optics and Spectroscopy (English translation of Optika i Spektroskopiya), Vol. 122, No. 3, 01.03.2017, p. 426-434.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Effect of the donor–acceptor properties of ligands on the spectroscopic and electrochemical properties of mixed-ligand complexes of Pt(II) and Ir(III) with cyclometalated 2-phenylbenzothiazole
AU - Katlenok, E. A.
AU - Smirnov, S. N.
AU - Ivanov, A. Yu
AU - Makarenko, S. V.
AU - Balashev, K. P.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - The results of the spectroscopic NMR (1H, 13C, and 195Pt), infrared, optical, and voltammetric characteristics of the mixed-ligand complexes of Pt(II) and Ir(III) with metalated 2-phenylbenzothiazole and tert-butylisocyanide (tBuNC), acetonitrile (AN), ethylenediamine (En), O-ethyldithiocarbamate (Exn–), and diethyldithiocarbamate (Dtc–) ions are presented. It is demonstrated that the change in donor–acceptor interaction of ligands tBuNC, AN, En, Exn–, and Dtc– with metal leads to an increase in the energy of the highest occupied molecular orbital of the complexes and is accompanied by a shift of the cathode potential of the metal-centered oxidation, a bathochromic shift of the spin-allowed and spin-forbidden metal-tocyclometalated ligand optical charge transfer transitions, and an increase the degree of mixing of the 1MLCT and triplet intraligand states, responsible for the phosphorescence of the complexes.
AB - The results of the spectroscopic NMR (1H, 13C, and 195Pt), infrared, optical, and voltammetric characteristics of the mixed-ligand complexes of Pt(II) and Ir(III) with metalated 2-phenylbenzothiazole and tert-butylisocyanide (tBuNC), acetonitrile (AN), ethylenediamine (En), O-ethyldithiocarbamate (Exn–), and diethyldithiocarbamate (Dtc–) ions are presented. It is demonstrated that the change in donor–acceptor interaction of ligands tBuNC, AN, En, Exn–, and Dtc– with metal leads to an increase in the energy of the highest occupied molecular orbital of the complexes and is accompanied by a shift of the cathode potential of the metal-centered oxidation, a bathochromic shift of the spin-allowed and spin-forbidden metal-tocyclometalated ligand optical charge transfer transitions, and an increase the degree of mixing of the 1MLCT and triplet intraligand states, responsible for the phosphorescence of the complexes.
UR - http://www.scopus.com/inward/record.url?scp=85016738196&partnerID=8YFLogxK
U2 - 10.1134/S0030400X17030110
DO - 10.1134/S0030400X17030110
M3 - Article
AN - SCOPUS:85016738196
VL - 122
SP - 426
EP - 434
JO - OPTICS AND SPECTROSCOPY
JF - OPTICS AND SPECTROSCOPY
SN - 0030-400X
IS - 3
ER -
ID: 36153056