The four new Ag(I) complexes Ag(phen)(P-nCB) (1), Ag(idmp)(P-nCB) (2), Ag(dmp)(P-nCB) (3), and Ag(dbp)(P-nCB) (4) with P-nCB = bis(diphenylphosphine)-nido-carborane, phen = 1,10-phenanthroline, idmp = 4,7-dimethyl-1,10-phenanthroline, dmp = 2,9-dimethyl-1,10-phenanthroline, and dbp = 2,9-di-n-butyl-1,10-phenanthroline were designed to demonstrate how to develop Ag(I) complexes that exhibit highly efficient thermally activated delayed fluorescence (TADF). The substituents on the 1,10-phenanthroline ligand affect the photophysical properties strongly (i) electronically via influencing the radiative rate of the S → S transition and (ii) structurally by rigidifying the molecular geometry with respect to geometry changes occurring in the lowest excited S and T states. The oscillator strength of the S ↔ S transition f(S ↔ S)-an important parameter for the TADF efficiency being proportional to the radiative rate-can be increased from f(S ↔ S) = 0.0258 for Ag(phen)(P-nCB) (1) to f(S ↔ S) = 0.0536 for Ag(dbp)(P-nCB) (4), as calculated for the T state optimized geometries. This parameter governs the radiative TADF decay time (τ) at ambient temperature, found to be τ = 5.6 μs for Ag(phen)(P-nCB) (1) but only τ = 1.4 μs for Ag(dbp)(P-nCB) (4)-a record TADF value. In parallel, the photoluminescence quantum yield (Φ) measured for powder samples at ambient temperature is boosted up from Φ = 36% for Ag(phen)(P-nCB) (1) to Φ = 100% for Ag(dbp)(P-nCB) (4). This is a consequence of a cooperative effect of both decreasing the nonradiative decay rate and increasing the radiative decay rate in the series from Ag(phen)(P-nCB) (1), Ag(idmp)(P-nCB) (2), and Ag(dmp)(P-nCB) (3) to Ag(dbp)(P-nCB) (4). Another parameter important for the TADF behavior is the activation energy of the S state from the state T, ΔE(S-T). Experimentally it is determined for the complexes Ag(dmp)(P-nCB) (3) and Ag(dbp)(P-nCB) (4) to be of moderate size of ΔE(S-T) = 650 cm.
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http://dx.doi.org/10.1021/acs.inorgchem.7b02002 | DOI Listing |
Inorg Chem
January 2025
Henan Provincial Key Laboratory of Surface and Interface Science, Zhengzhou University of Light Industry, Zhengzhou 450002, P. R. China.
Three two-dimensional (2D) chiral Ag(I) complexes with formulas [Ag(L)(5-nipa)] (), [Ag(L)(5-nipa)] (), and {[Ag(L)(5-hipa)]·2HO} () were prepared through the reactions of AgO with enantiopure -monodentate N-donors (L/L) and different dicarboxylic acids bearing A (acceptor)-π-- and D (donor)-π--type structural features, where / = (-)/(+)-2-(4'-pyridyl)-4,5-pinene-pyridine, 5-Hnipa = 5-nitroisophthalic acid, and 5-Hhipa = 5-hydroxyisophthalic acid. A study of their nonlinear optical responses reveals that chiral and enantiomeric pairs with the A-π--type dicarboxylic acid ligand simultaneously display second- and third-harmonic generation (SHG and THG) responses, while chiral containing the D-π--type dicarboxylic acid ligand only exhibits a very strong THG response. The THG intensity of is 451 × α-SiO, being about 27 and 24 times larger than those of and , respectively.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, 3012 Bern, Switzerland.
Binuclear silver(I) and copper(I) complexes, and , with bridging diphenylphosphine ligands were prepared. In , the silver(I) center is located inside a trigonal plane composed of three phosphorus donors from three separate and bridging dppm ligands. The fourth coordination site is filled with neighboring silver(I) ions.
View Article and Find Full Text PDFMolecules
December 2024
Centre for AMR and One Health Research, Technological University Dublin, TU Dublin, Tallaght Campus, D24 FKT9 Dublin, Ireland.
Heteroleptic coumarin-based silver(I) complexes with improved solubility profiles were synthesised using either triphenylphosphine or an -heterocyclic carbene as adduct ligands, and were fully characterised using IR and NMR spectroscopy, elemental analysis, and, where possible, X-ray crystallography. The triphenylphosphine adducts formed well-resolved structures, where the oxyacetate ligands asymmetrically chelated the silver(I) ion in a bidentate chelating mode, and the silver(I) ion was also bound to two triphenylphosphine ligands. The solubility profile and photostability of the adducts were considerably improved compared to those of previously isolated simple coumarin silver(I) complexes.
View Article and Find Full Text PDFDalton Trans
December 2024
Institute for Molecular Science, Okazaki, Aichi 444-8585, Japan.
A luminescent silver(I) complex containing a luminescent radical ligand was prepared for the first time. Coordination to Ag enhanced and red-shifted the radical-centered emission. This study demonstrates similar effects in the luminescence of the radical by complexation with group 11 d-metal ions.
View Article and Find Full Text PDFInorg Chem
December 2024
Department of Chemistry, National Taiwan University, 1, Sec. 4, Roosevelt Rd., Taipei 10617, Taiwan.
AuCl(PMe) and AuCl(PEt) were used to react with quinoline-8-thiolate (8-QNS) to give three Au(I) complexes, i.e., [8-QNS(AuPMe)]ClO (), [(8-QNS)Ag(AuPMe)]ClO (), and [8-QNS(AuPEt)]ClO (), which have been structurally determined by X-ray diffraction to show various intra- and intermolecular metal···metal contacts (i.
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