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Dispirocycles: Novel Platforms for Construction of High-Performance Host Materials for Phosphorescent Organic Light-Emitting Diodes
摘要： Spirocycle compounds such as 9,9′-Spirobifluorene (SBF) are becoming more and more attractive for use as the host materials in organic optoelectronic devices. In this manuscript, two dispirocycles, namely dispiro[fluorene-9,9?-anthracene-10?,9??-fluorene] and 10,10??-diphenyl-10H,10??H-dispiro[acridine-9,9?-anthracene-10?,9??-acridine] were used for the construction of hosts materials (1, 2, 3, and 4). The attached triphenylamine group would determine the thermal, photophysical, electrochemical, and charge transport properties, and therefore they have different electroluminescence performances. The device based on dispiro[fluorene-9,9?-anthracene-10?,9??-fluorene] (2) and 10,10??-diphenyl-10H,10??H-dispiro[acridine-9,9?-anthracene-10?,9??-acridine] (3) molecular platforms exhibited a external quantum efficiency of over 21% with a very high power efficiency (~100 lm W-1). The results here demonstrate to us the potential of extending the possibilities of applying the dispirocyclic molecular platforms with inherent rigidity for developing highly efficient host materials for OLEDs.
关键词： Dispirocycles,OLEDs,Host materials,Phosphorescence,Triplet energy
更新于2025-11-19 16:56:42
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Phosphorimetric determination of 4-nitrophenol using mesoporous molecular imprinting polymers containing manganese(II)-doped ZnS quantum dots
摘要： Mesoporous molecularly imprinted polymers (MIPs) containing mangnanese-doped ZnS quantum dots (Mn-ZnS QDs) were prepared for specific recognition and detection of 4-nitrophenol (4-NP). The Mn-ZnS QDs display orange room-temperature phosphorescence with excitation/emission peaks at 295/590 nm and a decay time of 2.0 ms. In the presence of 4-NP, the orange phosphorescence is strongly reduced. Phosphorescence drops linearly in the 0.1–100 μM 4-NP concentration range, and the detection limit is 60 nM. The detection limit is far lower than the maximally allowed 4-NP concentrations in surface water and drinking water as specified by the U.S. Environmental Protection Agency. The intraday (n = 5) and interday (n = 6) spiked recovery rates were 96.0–104.5% and 97.9–107.9%, respectively, with relative standard deviations of 0.7–4.8% and 1.8–7.5% respectively. These MIPs integrated the characteristic features of phosphorimetry and molecular imprinting. Potential interference by competitive substances, background fluorescence or scattered light are widely reduced.
关键词： Room-temperature phosphorescence,Mesoporous molecularly imprinted polymers,Photoinduced electron-transfer,4-Nitrophenol,Decay time
更新于2025-11-14 17:04:02
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Aggregation-induced phosphorescence quenching method for the detection of picric acid based on melamine-passivated Mn-doped ZnS quantum dots
摘要： Melamine (MA)-passivated Mn-doped ZnS quantum dots (QDs) were synthesized by a hydrothermal method. The MA-passivated QDs can form a charge-transfer complex with picric acid (PA) at 80 °C, thereby quenching the phosphorescence of the QDs. A sensitive method for detecting PA was established based on this principle of phosphorescence quenching. When the PA concentration ranged from 2.0–180 ng mL–1, the concentration was linearly related to the quenching intensity of the QDs, with a detection limit of 1.4 ng mL–1. When applied to detect PA in environmental water samples, the proposed method showed superior analytical performance compared with other PA analysis methods. Furthermore, we verified the static quenching mechanism by density functional theory. MA on the surface of QDs and PA formed a stable structure with a binding energy of 12.43 eV.
关键词： Melamine,Picric Acid,Mn-doped quantum dots,Charge-transfer Complex,Phosphorescence
更新于2025-11-14 17:04:02
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{Zn <sub/>6</sub> } Cluster Based Metal–Organic Framework with Enhanced Room-Temperature Phosphorescence and Optoelectronic Performances
摘要： Molecule-based solid-state materials with long lifetimes could enable longer migration distances for excitons, which are beneficial for vast applications in optoelectronic field. Herein, we report a hexanuclear zinc cluster based MOF exhibits highly enhanced phosphorescence about 2 orders of magnitude in comparison with the pristine phosphor ligand. The combination of both experimental and computational results suggest that the {Zn6} cluster is very important for adjusting molecular conformations, packing arrangement, and photophysical properties of the organic phosphor ligands within the MOF matrix. Optoelectronic measurements reveal that the MOF-modified electrode is catalytically active to hydrogen evolution under light irradiation in neutral solution. Thus, our study provide an effective way to achieve low-cost metal-based phosphorescence MOF, expanding its further optoelectronic applications.
关键词： optoelectronic performances,metal?organic framework,hexanuclear zinc cluster,room-temperature phosphorescence
更新于2025-11-14 15:23:50
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Extrinsic heavy metal atom effect on the solid state room temperature phosphorescence of cyclic triimidazole
摘要： Four coordination compounds [Zn3(CH3COO)6(H2O)2](TT)2, [Cd(H2O)6](ClO4)2(TT)2, [Cd(H2O)6](BF4)2(TT)2, [Zn(H2O)6](BF4)2(TT)2 (1-4) accommodating triimidazo[1,2-a:1',2'-c:1'',2''-e][1,3,5]triazine (TT) as a guest in their crystal lattice are isolated and fully photophysically and structurally characterized. Their emission properties are compared with those of afterglow TT and interpreted taking into account the heavy atom effect and crystal packing similarities and differences. In the case of 1, due to the closeness of the TT H-aggregates arrangement with that of the phosphor's pure phase, the observed intensification of the phosphorescent emission at the expense of the prompt one is attributed to the extrinsic heavy atom effect of Zn. In 2 and 3, the heavier Cd atom is responsible for a decrease in the lifetimes of the afterglow emission, despite the presence of tightly overlapped H-dimers in the crystal structure. Finally for 4, isostructural with 3, the Zn atom reveals in RTUP lifetime comparable with that of 1.
关键词： extrinsic heavy atom effect,H aggregates,time resolved photoluminescence,room temperature ultralong phosphorescence,single crystal XRD
更新于2025-09-23 15:23:52
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Polymorphic Pure Organic Luminogens with Through Space Conjugation and Persistent Room Temperature Phosphorescence
摘要： Pure organic luminogens with persistent room temperature phosphorescence (p-RTP) have attracted increasing attention owing to their fundamental significance and potential applications in security inks, bioimaging, and photodynamic therapy. Previous p-RTP luminogens are normally with through bond conjugation. In this work, we report a pure organic luminogen, AN-MA, the Diels-Alder cycloaddition adduct of anthracene (AN) and maleic anhydride (MA), which possesses isolated phenyls and anhydride moiety. AN-MA exhibits aggregation-enhanced emission (AEE) characteristics, with efficiency of ~2% and up to 8.5% in solution and crystals, respectively. Two polymorphs of AN-MA are readily obtained, which can generate UV emission from individual phenyl rings together with bright blue emission owing to the effective through space conjugation. Moreover, p-RTP with lifetime of up to ~1.6 s is obtained in crystals. These results not only disclose a new system with both fluorescence and RTP dual emission, but also suggest an alternative through space conjugation strategy towards pure organic p-RTP luminogens with tunable emissions.
关键词： anticounterfeiting,pure organic luminogens,persistent room temperature phosphorescence,through space conjugation,polymorphism
更新于2025-09-23 15:23:52
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Paintable Room Temperature Phosphorescent Liquid Formulations of Alkylated Bromonaphthalimide
摘要： Organic phosphors have been widely explored with an understanding that crystalline molecular ordering is a requisite for enhanced intersystem crossing. In this context, we explore the room temperature phosphorescence features of a solvent-free organic liquid phosphor in air. Given alkyl chain substitution varied the physical states of bromonaphthalimides, phosphorescence remained unaltered for the solvent-free liquid in air. As the first report, a solvent-free liquid of a long swallow tailed bromonaphthalimide exhibits room temperature phosphorescence in air. Doping of the phosphor with carbonyl guests resulted in enhanced phosphorescence and hence a large area paintable phosphorescent liquid composite with improved lifetime and quantum yield is developed.
关键词： phosphorescence,organic liquids,excimer,luminescent thermometer,liquid phosphor
更新于2025-09-23 15:23:52
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Subtle structure tailoring of metal-free triazine luminogens for highly efficient ultralong organic phosphorescence
摘要： Highly efficient ultralong organic phosphorescence (UOP) based on a series of metal-free triazine luminogens was achieved via subtly structural tailoring of bromine substituted positions. Impressively, p-BrAT in solid state displayed high phosphorescence efficiency up to 9.7% with a long lifetime of 386 ms, which was one of the highest efficient UOP materials reported so far in metal-free compounds.
关键词： Isomerism,Ultralong organic phosphorescence (UOP),Crystal engineering,H-Aggregation,Intermolecular interactions
更新于2025-09-23 15:23:52
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Synthesis, characterization, and photophysical properties of bismetalated platinum complexes with benzothiophene ligands
摘要： Benzothiophene-based ligands containing quinoline or pyridine moieties were synthesized through Suzuki Coupling reactions and subsequently reacted with the binuclear Platinum compound, [Pt2Me4(μ-SMe2)2], PtA, in order to study chelate-assisted C-H activation. The preparation and characterization of C^N cyclometalated products, including η2 intermediates, monometalated, and bismetalated species, are reported. The photophysical properties of the complexes were studied and compared to TD-DFT computational results.
关键词： TD-DFT,phosphorescence,benzothiophene,C-H activation,cyclometalation
更新于2025-09-23 15:23:52
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New blue phosphorescence from trifluorosulfonyl-substituted iridium complexes
摘要： For color-pure phosphorescence organic light emitting diodes (PHOLEDs), we synthesized the trifluoromethyl sulfonyl substituted ligand and two new blue Iridium complexes with perfluoro-sulfonyl group (SOCF3pic and SOCF3mpic). The both iridium complexes showed similar photophysical and thermal properties while the HOMO energy leves of two Iridium complexes slightly differnet to be -5.84 eV for SOCF3pic and -5.74 eV for SOCF3mpic, respectively. The device with the SOCF3mpic dopant exhibited higher device efficiencies of 7.17 cd/A and 3.7 % compared to that with the SOCF3pic dopant (4.03 cd/A and 2.78 %). Two-dimensional GIXD images of scattered X-ray intensity from surface to full depth for SOCF3pic-doped and SOCF3mpic-doped TCTA:4PTPS films were characterized for preferential orientation along the out-of-plane direction.
关键词： preferential orientation along the out-of-plane direction,blue phosphorescence,iridium complex,grazing incidence wide-angle X-ray diffraction,organic light emitting diodes
更新于2025-09-23 15:23:52