RESUMO
Metal-free organic emitters with thermally activated delayed fluorescence (TADF) characteristics are emerging due to the potential applications in optoelectronic devices, time-resolved luminescence imaging, and solid-phase sensing. Herein, we synthesized two (4-bromobenzoyl)pyridine (BPy)-based donor-acceptor (D-A) compounds with varying donor size and strength: the emitter BPy-pTC with tert-butylcarbazole (TC) as the donor and BPy-p3C with bulky tricarbazole (3C) as the donor unit. Both BPy-pTC and BPy-p3C exhibited prominent emission with TADF properties in solution and in the solid phase. The stronger excited-state charge transfer was obtained for BPy-p3C due to the bulkier donor, leading to a more twisted D-A geometry than that of BPy-pTC. Hence, BPy-p3C exhibited aggregation-induced enhanced emission (AIEE) in a THF/water mixture. Interestingly, the singlet-triplet energy gap (ΔE ST) was reduced for both compounds in the aggregated state as compared to toluene solution. Consequently, a faster reverse intersystem crossing rate (k RISC) was obtained in the aggregated state, facilitating photon upconversion, leading to enhanced delayed fluorescence. Further, the lone-pair electrons of the pyridinyl nitrogen atom were found to be sensitive to acidic protons. Hence, the exposure to acid and base vapors using trifluoroacetic acid (TFA) and triethylamine (TEA) led to solid-phase fluorescence switching with fatigue resistance. The current study demonstrates the role of the donor strength and size in tuning ΔE ST in the aggregated state as well as the relevance for fluorescence-based acid-base sensing.
RESUMO
Three multichromophore thermally activated delayed fluorescence (TADF) molecules, p-di2CzPN, m-di2CzPN, and 1,3,5-tri2CzPN, were synthesized and characterized. These molecules were designed by connecting the TADF moiety 4,5-di(9H-carbazol-9-yl)phthalonitrile (2CzPN) to different positions of a central benzene ring scaffold. Three highly soluble emitters all exhibited near-quantitative photoluminescence quantum yields (ΦPL) in toluene. High ΦPLs were also achieved in doped films, 59 and 70% for p-di2CzPN and m-di2CzPN in 10 wt % DPEPO doped film, respectively, and 54% for 1,3,5-tri2CzPN in 20 wt % doped CBP films. The rate constant of reverse intersystem crossing (kRISC) for p-di2CzPN and m-di2CzPN in DPEPO films reached 1.1 × 105 and 0.7 × 105 s-1, respectively, and kRISC for 1,3,5-tri2CzPN in the CBP film reached 1.7 × 105 s-1. A solution-processed organic light-emitting diode based on 1,3,5-tri2CzPN exhibited a sky-blue emission with CIE coordinates of (0.22, 0.44) and achieved a maximum external quantum efficiency of 7.1%.
RESUMO
We report the characterization of rotaxanes based on a carbazole-benzophenone thermally activated delayed fluorescence luminophore. We find that the mechanical bond leads to an improvement in key photophysical properties of the emitter, notably an increase in photoluminescence quantum yield and a decrease in the energy difference between singlet and triplet states, as well as fine tuning of the emission wavelength, a feat that is difficult to achieve when using covalently bound substituents. Computational simulations, supported by X-ray crystallography, suggest that this tuning of properties occurs due to weak interactions between the axle and the macrocycle that are enforced by the mechanical bond. This work highlights the benefits of using the mechanical bond to refine existing luminophores, providing a new avenue for emitter optimization that can ultimately increase the performance of these molecules.
RESUMO
Racemic and enantiopure phosphorescent iridium(III)-silver(I) coordination polymers are reported. The polymers rac-, Λ-, and Δ-IrAg were formed, respectively, by the assembly of the chiral iridium metalloligands rac-, Λ-, and Δ-[Ir(mesppy)2 (qpy)]PF6 (rac-, Λ- and Δ-Ir) where mesppy is 2-phenyl-4-mesitylpyridinato and qpy is 4,4':2',2'':4'',4'''-quaterpyridine, and Ag+ ions through Npy -Ag linear coordination. The polymers have been characterized in MeNO2 solution by 1 H and 1 H DOSY NMR and CD spectroscopies and in the solid-state by scanning electron microscopy (SEM). The crystal structures of the racemic polymer rac-IrAg has been obtained by X-ray diffraction. The polymers rac-, Λ-, and Δ-IrAg exhibited orange/red emission in solution, in films and as crystals, with intensities comparable to those of the corresponding iridium metalloligands rac-, Λ-, and Δ-Ir. The morphology of the enantiopure polymers in the solid-state resembles marigold flower-like nano-porous assemblies while the racemic polymer possesses an irregular morphology formation.
Assuntos
Ouro/química , Irídio/química , Luminescência , Compostos Organometálicos/química , Polímeros/química , Prata/química , Microscopia Eletrônica de Varredura , Conformação Molecular , Compostos Organometálicos/síntese química , Tamanho da Partícula , Propriedades de Superfície , Difração de Raios XRESUMO
Two benzoylpyridine-carbazole based fluorescence materials DCBPy and DTCBPy, bearing two carbazolyl and 4-(t-butyl)carbazolyl groups, respectively, at the meta and ortho carbons of the benzoyl ring, were synthesized. These molecules show very small ΔEST of 0.03 and 0.04 eV and transient PL characteristics indicating that they are thermally activated delayed fluorescence (TADF) materials. In addition, they show extremely different photoluminescent quantum yields in solution and in the solid state: in cyclohexane the value are 14 and 36%, but in the thin films, the value increase to 88.0 and 91.4%, respectively. The OLEDs using DCBPy and DTCBPy as dopants emit blue and green light with EQEs of 24.0 and 27.2%, respectively, and with low efficiency roll-off at practical brightness level. The crystal structure of DTCBPy reveals a substantial interaction between the ortho donor (carbazolyl) and acceptor (4-pyridylcarbonyl) unit. This interaction between donor and acceptor substituents likely play a key role to achieve very small ΔEST with high photoluminescence quantum yield.
RESUMO
A highly diastereoselective method for the synthesis of dihydroepoxybenzofluorenone derivatives from aromatic/vinylic amides and bicyclic alkenes is described. This new transformation proceeds through cobalt-catalyzed C-H activation and intramolecular nucleophilic addition to the amide functional group. Transition-metal-catalyzed C-H activation reactions of secondary amides with alkenes usually lead to [4+2] or [4+1] annulation; to the best of our knowledge, this is the first time that a [3+2] cycloaddition is described in this context. The reaction proceeds under mild conditions and tolerates a wide range of functional groups. Mechanistic studies imply that the C-H bond cleavage may be the rate-limiting step.
RESUMO
A highly regio- and stereoselective synthesis of 3,3-disubstituted phthalides from aryl carboxylic acids and allenes using a rhodium(III) catalyst has been demonstrated. The reaction features broad functional group tolerance and provides a simple and straightforward route to the synthesis of various 3-vinyl-substituted phthalides. Furthermore, the catalytic reaction can also be applied to the synthesis of biologically active 5-vinyl-substituted 2-furanones from α,ß-unsaturated carboxylic acids and allenes. The reactions proceed through a carboxylate-assisted ortho-CH activation and [4+1] annulation. The preliminary mechanistic studies suggest that a CH cleavage is the rate-determining step.
RESUMO
The gelation of two TADF positional isomers, 4BPy-mDTC and BPy-DTC, was explored. Among these emitters, only 4BPy-mDTC forms stable organogels due to the optimized intermolecular interactions. Interestingly, the morphology of the gel can be tuned from fibre to fettuccine by changing the solvents. The electrical conductivity of the self-assembly can also be increased from 8.05 × 10-4 S m-1 to 6.05 × 10-3 S m-1 by tuning the morphology.
RESUMO
The design of multifunctional materials is a challenging and important objective for a wide array of multidisciplinary applications. However, a multifunctional organic emitter exhibiting simultaneous aggregation-induced emission (AIE), multi-responsive polymorphs, mechanoluminescence and electroluminescence have been scarce. In this study, two anthracene based compounds, namely 10-(4-(9H-carbazol-9-yl)phenyl)anthracene-9-carbonitrile (CzPACN) and 10-(4-(di-p-tolylamino)phenyl)anthracene-9-carbonitrile (DTPACN) was designed and synthesized with rigid and flexible donors, respectively. The CzPACN shows the bright blue emission and DTPACN shows the bright green emission in solution. We have demonstrated an effective strategy to achieve three polymorphic phases such as DTPACN-α, DTPACN-ß and DTPACN-γ from DTPACN by controlling the temperature. Under mechanical stimuli, highly restricted and non-planar crystals of the structurally tuned polymorphs DTPACN-α, and DTPACN-ß exhibited red shifted emission and DTPACN-γ showed blue shifted emission. Conversely, CzPACN is not showing polymorphism and is not sensitive to external stimuli. In addition, blue and green OLEDs were fabricated using CzPACN and DTPACN, respectively, as an emitter and achieved a maximum external quantum efficiency (EQEmax ) of 5.5% and 5.7%, respectively, for blue and green OLEDs. Further, this study suggests designing multi-responsive smart materials via a simple modification by introducing a non-planar unit with a large twist.
RESUMO
Photofunctional co-crystal engineering strategies based on donor-acceptor π-conjugated system facilitates expedient molecular packing, consistent morphology, and switchable optical properties, conferring synergic 'structure-property relationship' for optoelectronic and biological functions. In this work, a series of organic co-crystals were formulated using a twisted aromatic hydrocarbon (TAH) donor and three diverse planar acceptors, resulting in color-tunable solid and aggregated state emission via variable packing and through-space charge-transfer interactions. While, adjusting the strength of acceptors, a structural transformation into hybrid stacking modes ultimately results in color-specific polymorphs, a configurational cis-isomer with very high photoluminescence quantum yield. The cis-isomeric co-crystal exhibits triplet-harvesting thermally activated delayed fluorescence (TADF) characteristics, presenting a key discovery in hydrocarbon-based multicomponent systems. Further, 1D-microrod-shaped co-crystal acts as an efficient photon-transducing optical waveguides, and their excellent dispersibility in water endows efficient cellular internalization with bright cell imaging performances. These salient approaches may open more avenues for the design and applications of TAH based co-crystals.
RESUMO
We report highly efficient, ultrathin non-doped green and bluish-green organic light-emitting diodes (OLEDs) using a thermally activated delayed fluorescence (TADF) emitter. The green OLED with an ultrathin (â¼1 nm) EML showed a 2.6-fold higher external quantum efficiency (EQEmax) of 13.5% with a luminance of 17 250 cd m-2 than the conventional (30 nm) non-doped device.
RESUMO
Three new quinoline TADF emitters, 2QPM-mDC, 2QPM-mDTC, and 4QPM-mDTC, were designed and synthesized and the emitters show Δ EST as low as 0.07 eV and high PL quantum yield (PLQY) up to 98%. An electroluminescence device based on 2QPM-mDTC can reach high EQE over 24%. Compared with the reported TADF devices, the device shows narrow emission bandwidth and high color purity. The excellent device performance is likely ascribed to the molecular design of 2QPM-mDTC containing an intramolecular H-bonding in the molecule.
RESUMO
We present a study of two isomeric thermally activated delayed fluorescence (TADF) emitters 9,9'-(sulfonylbis(pyrimidine-5,2-diyl))bis(3,6-di-tert-butyl-9H-carbazole) (pDTCz-DPmS) and 9,9'-(sulfonylbis(pyrazine-5,2-diyl))bis(3,6-di-tert-butyl-9H-carbazole) (pDTCz-DPzS). The use of pyrimidine and pyrazine as bridging units between the electron donor and acceptor moieties is found to be advantageous compared to the phenyl- (pDTCz-DPS) and pyridine-based analogues (pDTCz-3DPyS and pDTCz-2DPyS). Conformational modulation of the donor groups as a function of the bridge results in high photoluminescence quantum yields (ΦPL > 68%) and small energy gaps between singlet and triplet excited states (ΔEST < 160 meV). OLEDs using pDTCz-DPmS and pDTCz-DPzS as emitters exhibit blue and green electroluminescence, respectively, with higher maximum external quantum efficiencies (EQEmax of 14% and 18%, respectively) and a reduced efficiency roll-off as compared to the reference devices using pDTCz-DPS, pDTCz-3DPyS, and pDTCz-2DPyS as the emitters. Our results provide a more complete understanding on the impact of the bridge structure in D-A-D TADF systems on the optoelectronic properties of the emitter and how the balance between color purity and EQE in the devices can be controlled, advancing the design strategies for TADF emitters.
RESUMO
We have successfully synthesized a series of blue thermally activated delayed fluorescence emitters, BPy-pC, BPy-pTC, BPy-p2C, and BPy-p3C, bearing a 4-benzoylpyridine core as the electron-accepting unit and carbazolyl, tert-butylcarbazolyl, dicarbazolyl, and tercarbazolyl groups as the electron-donating units, respectively. The density functional theory calculation shows that all of the compounds have their lowest unoccupied molecular orbitals on the benzoylpyridine moiety. However, the highest occupied molecular orbital (HOMO) of BPy-p3C is widely dispersed to the whole tercarbazolyl group, while the HOMOs of BPy-pC and BPy-pTC are mainly on the carbazolyl and extended to the phenyl ring. As a result, ΔEST is reduced from 0.29 eV for BPy-pC to 0.05 eV for BPy-p3C, and the organic light-emitting diodes using these materials as dopants emit blue light and their maximum external quantum efficiencies (EQEs) increase from 4.2% to 23.9% for BPy-pC and BPy-p3C, respectively. The EQE of the BPy-p3C-based device increases 2 times more than that of the BPy-pTC-based device without a significant change in the color coordinates.
RESUMO
Three m-terphenyl oxadiazole derivatives, 3,3â³-bis(5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)-1,1':3',1â³-terphenyl (4PyOXD), 3,3â³-bis(5-(pyridin-3-yl)-1,3,4-oxadiazol-2-yl)-1,1':3',1â³-terphenyl (3PyOXD), and 3,3â³-bis(5-phenyl-1,3,4-oxadiazol-2-yl)-1,1':3',1â³-terphenyl (PhOXD), were synthesized. They exhibit relatively high electron mobilities compared with those of known electron-transport materials such as TAZ, BAlq, and BCP+Alq3. These materials were then utilized as electron transporters and hole/exciton blockers for blue, green, and red phosphorescent organic light-emitting diodes. The devices exhibited reduced driving voltages, very high efficiency, and negligible roll-off. More importantly, among these three oxadiazole derivatives, PhOXD performed as an ideal electron-transporting material for the blue, green, and red devices with excellent external quantum efficiencies (EQEs, >26%) as well as current and power efficiencies. Using these materials as an electron-transporting/exciton-blocking layer, low roll-off was achieved for the devices, indicative of excellent confinement of the triplet excitons in the emitting layer even at high current densities. At the normal operation brightness of 1000 cd m(-2), the EQEs remained >21.3% for these basic color devices. In addition, the relationships between physical properties and structures of the molecules such as the electron mobility, triplet energy gap, and efficiency can be clearly rationalized.