Manipulating the relaxation pathways of excited states and understanding mechanisms of photochemical reactions present important challenges in chemistry. Here we report a unique zinc(II) complex exhibiting unprecedented interplay between the excitation-wavelength-dependent emission, thermally activated delayed fluorescence (TADF) and excited state intramolecular proton transfer (ESIPT). The ESIPT process in the complex is favoured by a short intramolecular OH⋅⋅⋅N hydrogen bond. Synergy between the excitation-wavelength-dependent emission and ESIPT arises due to heavy zinc atom favouring intersystem crossing (isc). Reverse intersystem crossing (risc) and TADF are favoured by a narrow singlet-triplet gap, ΔE ≈10 kJ mol . These results provide the first insight into how a proton-transfer system can be modified to show a synergy between the excitation-wavelength-dependent emission, ESIPT and TADF. This strategy offers new perspectives for designing ESIPT and TADF emitters exhibiting tunable excitation-wavelength-dependent luminescence.
The magnetic and thermodynamic properties of the prototypical 1D polymeric complex Fe(ATrz)(NO)·HO (ATrz = 4-amino-1,2,4-triazole) were reinvestigated to gain an insight into the impact of water molecules on the spin transition. Variations in the outerspheric water molecule content in the complex induce drastic and unpredictable changes in its spin crossover regimes. Under vacuum the complex loses water molecules and shows a wide (ca. 30 K) and reproducible hysteresis loop, T↑ = 337-345 K and T↓ = 316-313 K. In sealed ampoules the complex Fe(ATrz)(NO)·HO shows a narrow hysteresis (ca. 1-4 K), T↑ = 326-329 K and T↓ = 326-324 K. After adsorption of water the complex Fe(ATrz)(NO)·nHO (n = 1.25-1.6) demonstrates a narrow two-step spin transition. In all these cases the kinetics of the LS → HS and HS → LS transitions has decelerating non-cooperative character. For the system Fe(ATrz)(NO)·nHO (n = 3.6-16.6) wide hysteresis (ca. 5-20 K) re-appears near room temperature (T↑ = 319-321 K and T↓ = 300-315 K). Surprisingly, the kinetics of the HS → LS spin transition for the systems with high water content switches from decelerating to sigmoidal (cooperative). The activation energy of the LS → HS transition was estimated for the first time for iron(ii) spin crossover complexes with 1,2,4-triazoles (ca. 1000-2000 kJ mol). The systems Fe(ATrz)(NO) and Fe(ATrz)(NO)·nHO show compensation effects (ΔH - ΔS, ln A - E). A correlation between the T↑, the ΔH values and the water content in the complex is observed: the highest ΔH values (27-29 kJ mol) and the lowest T↑ values (317-320 K) correspond to the samples with high water content, whereas the lowest ΔH values (19-23 kJ mol) and the highest T↑ values (337-345 K) correspond to water-free samples, Fe(ATrz)(NO). Our results provide the first experimental evidence that the presence of water (and even air humidity) produces dramatic changes in the spin crossover behavior of the prototypical 1D polymeric complex Fe(ATrz)(NO)·HO (ATrz = 4-amino-1,2,4-triazole).
A series of ESIPT-capable zinc(II) complexes [Zn(HL)Hal2] (Hal = Cl, Br, I) with a rationally designed ESIPT-ligand 1-hydroxy-5-methyl-2,4-di(pyridin-2-yl)-1H-imidazole (HL) featuring spatially separated metal binding and ESIPT sites has been synthesized...
A series of mononuclear heteroleptic copper(I) halide complexes, [CuL(PPh3)X] (X = Cl, Br, I), based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L) and triphenylphosphine, have been synthesized by reaction between CuX (X = Cl, Br, I), L and PPh3 in a molar ratio of 1/1/1 in MeCN solutions. The copper atom, showing the distorted tetrahedral environment, is bound by the N,N-chelating ligand L, triphenylphosphine and a halide ion. The complexes [CuL(PPh3)Cl] and [CuL(PPh3)Br] are isostructural. In CH2Cl2 solutions, L and the complexes [CuL(PPh3)X] (X = Cl, Br, I) display a luminescence band with λ(max) = 377 nm and a lifetime of 1.9 ns (ligand-based luminescence (LL*)). However, the complex [CuL(PPh3)I] has an additional weak luminescence band with λ(max) = 681 nm and a lifetime of 96 ns of (3)MLCT origin. In the solid state, L shows the splitting of the luminescence band to λ(max) = 365 and 384 nm and a slight increase of the lifetime to 2.66 ns. Solid samples of the complexes [CuL(PPh3)X] demonstrate (3)MLCT luminescence bands at 620 nm (X = Cl), 605 nm (X = Br) and 559 nm (X = I) with lifetimes in the range 3.6-11.2 μs, whereas the LL* band (377 nm) is absent. Quantum yields and rate constants of radiative and nonradiative processes were determined in CH2Cl2 solutions and in the solid state for all complexes. The luminescence quantum yield and lifetimes for the solid samples increase in the order [CuL(PPh3)Cl] < [CuL(PPh3)Br] < [CuL(PPh3)I]. This is due to the increase of radiative decay and simultaneous suppression of nonradiative decay. The complex [CuL(PPh3)I] shows a high quantum yield of 29.4% and an excited state lifetime of 11.2 μs.
The emission of the ESIPT-fluorophores is known to be sensitive to various external and internal stimuli and can be fine-tuned through the substitution in the proton-donating and proton-accepting groups. The...
A mononuclear manganese(ii) complex with a chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand (L), [MnLCl]·HO, shows intriguing excitation wavelength-dependent emission. Depending on the excitation wavelength, the complex demonstrates three emission bands with the maxima at 380 nm, 440 nm and 495 nm. The 380 nm and 440 nm emissions originate from the π → π* and n → π* ligand-centered transitions. The long-wave 495 nm emission with microsecond lifetimes is related to the d-d transitions and/or metal-to-ligand and halogen-to-ligand charge transfer. The emission behavior of this complex is strongly temperature-dependent: upon cooling from 300 K down to 77 K, the intensity of emission considerably increases. The enhancement of the luminescence upon cooling is accompanied by the appearance of the vibrational structure. This complex is the first example of manganese(ii) complexes demonstrating excitation wavelength-dependent emission.
First examples of copper(I) complexes with 2-(alkylsulfanyl)pyrimidine ligands have been synthesized. Reactions of copper(I) iodide with 2-(methylsulfanyl)pyrimidine (L1) in various metal-to-ligand molar ratios in MeCN afford a ladder-type coordination polymer...
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