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In this study, we developed a molecular design strategy for tetradentate Pt(II) complexes to improve the efficiency and color purity of blue phosphorescent organic light-emitting diodes (PhOLEDs). The strategy involves the introduction of a conformation manager at the 4-position of benzimidazolyl carbene in a tetradentate ligand. Methyl and phenyl groups were employed as conformation managers to enhance the rigidity of the molecule, thereby improving the radiative process and suppressing vibrational emission. The conformation managers inhibited π-conjugation extension to the -substituent, blue-shifting the emission spectrum and stabilizing the lowest unoccupied molecular orbital level of the ligand. The Pt(II) complexes embedded with the conformation managers achieved small full-width at half maximum (FWHM) values, blue-shifted emission spectra, and high external quantum efficiencies (EQEs). The blue PhOLEDs with methyl- and phenyl-incorporated Pt(II) complexes exhibited small FWHMs of 18 and 20 nm, high EQEs of 27.1% and 27.5%, and CIE coordinates of 0.084 and 0.100, respectively, indicating that the devices outperform other reported Pt(II) complex based blue PhOLED devices. These results demonstrate that, by embedding a conformation manager in tetradentate ligands, blue PhOLED devices with narrowband emission, high EQEs, and improved color purity can be achieved.
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http://dx.doi.org/10.1039/d4mh01817f | DOI Listing |
J Inorg Biochem
August 2025
Inner Mongolia University, Research Center for Glycochemistry of Characteristic Medicinal Resources, Department of Chemistry and Chemical Engineering, Hohhot, People's Republic of China. Electronic address:
In this study, we modified ONS-donor tridentate salicylaldimine main ligand-based Pt(II) complexes with monosaccharide functionalized pyridine co-ligand. All these complexes (C1-C12) were prepared in two steps continuous reaction by firstly, abstracting the ancillary chloride of the starting complexes with AgBF and secondly, adding the acetylated β-d-glucose conjugated pyridine. All these complexes were analyzed for their in vitro anticancer potency in human's gastric cancer MKN 45, colon cancer RPMI 4788 and non-small cell lung cancer A549 cells.
View Article and Find Full Text PDFDalton Trans
September 2025
University of Cologne, Faculty for Mathematics and Natural Sciences, Department of Chemistry and Biochemistry, Institute for Inorganic and Materials Chemistry, Greinstrasse 6, D-50939 Köln, Germany.
In the frame of our research aiming to develop efficient triplet-emitting materials, we are exploring the role of the second coordination sphere in enhancing the rigidity of structures and its controlling aspect over the extents of excited state distortions. We thus synthesised three N^C^N cyclometalated complexes [M(L)Cl] (M = Pt, Pd, and Ni), where the two -positions of the pyridyl moieties in 1,3-di(2-pyridyl)-benzene are benzyl substituted (Bn) forming a tight binding pocket for the metal and the Cl ancillary ligand. The molecular structures from single-crystal X-ray diffraction show a markedly distorted square planar M(II) coordination with values of around 0.
View Article and Find Full Text PDFChembiochem
August 2025
Department of Chemistry, Royal College of Surgeons in Ireland, Dublin 2, D02 YN77, Ireland.
The development of the first Pt(II) tetrazine complex, trans-[Pt(II)Cl(dmso)(CH-Tz-Bz-NH)] (1), is reported, which exhibits good in vitro cytotoxicity against MDA-MB-231 cells and succesfully undergoes inverse electron demand Diels-Alder (IEDDA) reactions with trans-cyclooctene (TCO) and bicyclononyne (BCN) derivates in solution. We demonstrate a live-cell IEDDA reaction of 1 with a BF-azadipyrromethene fluorophore (NIR-AZA) posessing a BCN handle. A live-cell bioorthogonal reaction is established using fluorescence lifetime imaging microscopy (FLIM), through a fluorescence lifetime change of 0.
View Article and Find Full Text PDFInorg Chem
September 2025
Departamento de Química Inorgánica, Escuela de Ingeniería y Arquitectura de Zaragoza, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC - Universidad de Zaragoza, Campus Río Ebro, Edificio Torres Quevedo, 50018 Zaragoza, Spain.
The Pt(II) dinuclear compounds [{Pt(C^N)(μ-S^N)}] [S^NH: 2-mercapto-1-methylimidazol; HC^N= 1-naphthalen-2-yl-1-pyrazole (naph-pz, ); benzo[]quinoline (bzq, )] were obtained by reaction of the corresponding mononuclear precursor [Pt(C^N)Cl(S^NH)] (C^N: naph-pz , bzq ) with NEt. Then, and were reacted with aqueous HX (X: Cl, Br, I) in molar ratio 1:2 to give the corresponding oxidized derivatives [{Pt(C^N)(μ-S^N)X}] (X = Cl , Br , I ). Their X-ray structures showed shorter Pt-Pt distances in the Pt(III) complexes (.
View Article and Find Full Text PDFJ Inorg Biochem
December 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom. Electronic address:
Photoactive Pt(IV) complexes conjugated to amino acid methyl esters trans,trans,trans-[Pt(py)(N)(OH)(succinate-amino acid methyl ester)] (amino acid = L-leucine (1), glycine (2), L-tyrosine (3) and L-tryptophan (4)) have been synthesised and characterised. Complexes 1-4 showed high dark stability, but were activated upon irradiation with blue light to generate azidyl and hydroxyl radicals and Pt(II) species. Interestingly, conjugated tryptophan in 4 quenched the formation of azidyl and hydroxyl radicals and Pt-guanosine 5'-monphosphate adducts, while the amino acids in complexes 1-3 showed no significant effects on the formation of their photoproducts.
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