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Sayaka Nagai - One of the best experts on this subject based on the ideXlab platform.
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sequential halochromic mechanochromic luminescence of pyridyl substituted solid state emissive dyes thermally controlled stepwise recovery of the original Emission Color
CrystEngComm, 2019Co-Authors: Suguru Ito, Chika Nishimoto, Sayaka NagaiAbstract:Stimuli-responsive organic dyes that switch the Color of their solid-state Emission upon exposure to external stimuli represent an important class of materials due to their potential applications in various areas of sensing technology. Although an increasing number of multi-stimuli-responsive organic dyes have been reported in recent years, only a few solid-state fluorophores are known to respond to two kinds of stimuli in a stepwise and reversible manner. Herein, we report the sequential halochromic (acidochromic)/mechanochromic luminescence behavior of a pyridyl-substituted solid-state fluorophore. The solid-state Emission Color of this pyridyl-substituted dye was systematically shifted in the bathochromic direction by forming cocrystals with several benzoic acid derivatives that exhibit different pKa values. Upon grinding these cocrystals with a spatula, further bathochromic shifts of their maximum Emission wavelengths were observed upon amorphization. Conversely, the Emission Color and crystallinity can be recovered upon heating the ground samples of the cocrystals to their cold-crystallization transition temperature (Tc ∼ 100 °C). Heating the ground cocrystals further (185–260 °C) removes the benzoic acid derivatives, which restores the original Emission Color of the pyridyl-substituted dye. In other words, we have developed a new system that exhibits a two-step Emission Color recovery in response to temperature by combining halochromic and mechanochromic luminescence in series.
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Sequential halochromic/mechanochromic luminescence of pyridyl-substituted solid-state emissive dyes: thermally controlled stepwise recovery of the original Emission Color
CrystEngComm, 2019Co-Authors: Suguru Ito, Chika Nishimoto, Sayaka NagaiAbstract:Stimuli-responsive organic dyes that switch the Color of their solid-state Emission upon exposure to external stimuli represent an important class of materials due to their potential applications in various areas of sensing technology. Although an increasing number of multi-stimuli-responsive organic dyes have been reported in recent years, only a few solid-state fluorophores are known to respond to two kinds of stimuli in a stepwise and reversible manner. Herein, we report the sequential halochromic (acidochromic)/mechanochromic luminescence behavior of a pyridyl-substituted solid-state fluorophore. The solid-state Emission Color of this pyridyl-substituted dye was systematically shifted in the bathochromic direction by forming cocrystals with several benzoic acid derivatives that exhibit different pKa values. Upon grinding these cocrystals with a spatula, further bathochromic shifts of their maximum Emission wavelengths were observed upon amorphization. Conversely, the Emission Color and crystallinity can be recovered upon heating the ground samples of the cocrystals to their cold-crystallization transition temperature (Tc ∼ 100 °C). Heating the ground cocrystals further (185–260 °C) removes the benzoic acid derivatives, which restores the original Emission Color of the pyridyl-substituted dye. In other words, we have developed a new system that exhibits a two-step Emission Color recovery in response to temperature by combining halochromic and mechanochromic luminescence in series.
Suguru Ito - One of the best experts on this subject based on the ideXlab platform.
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sequential halochromic mechanochromic luminescence of pyridyl substituted solid state emissive dyes thermally controlled stepwise recovery of the original Emission Color
CrystEngComm, 2019Co-Authors: Suguru Ito, Chika Nishimoto, Sayaka NagaiAbstract:Stimuli-responsive organic dyes that switch the Color of their solid-state Emission upon exposure to external stimuli represent an important class of materials due to their potential applications in various areas of sensing technology. Although an increasing number of multi-stimuli-responsive organic dyes have been reported in recent years, only a few solid-state fluorophores are known to respond to two kinds of stimuli in a stepwise and reversible manner. Herein, we report the sequential halochromic (acidochromic)/mechanochromic luminescence behavior of a pyridyl-substituted solid-state fluorophore. The solid-state Emission Color of this pyridyl-substituted dye was systematically shifted in the bathochromic direction by forming cocrystals with several benzoic acid derivatives that exhibit different pKa values. Upon grinding these cocrystals with a spatula, further bathochromic shifts of their maximum Emission wavelengths were observed upon amorphization. Conversely, the Emission Color and crystallinity can be recovered upon heating the ground samples of the cocrystals to their cold-crystallization transition temperature (Tc ∼ 100 °C). Heating the ground cocrystals further (185–260 °C) removes the benzoic acid derivatives, which restores the original Emission Color of the pyridyl-substituted dye. In other words, we have developed a new system that exhibits a two-step Emission Color recovery in response to temperature by combining halochromic and mechanochromic luminescence in series.
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Sequential halochromic/mechanochromic luminescence of pyridyl-substituted solid-state emissive dyes: thermally controlled stepwise recovery of the original Emission Color
CrystEngComm, 2019Co-Authors: Suguru Ito, Chika Nishimoto, Sayaka NagaiAbstract:Stimuli-responsive organic dyes that switch the Color of their solid-state Emission upon exposure to external stimuli represent an important class of materials due to their potential applications in various areas of sensing technology. Although an increasing number of multi-stimuli-responsive organic dyes have been reported in recent years, only a few solid-state fluorophores are known to respond to two kinds of stimuli in a stepwise and reversible manner. Herein, we report the sequential halochromic (acidochromic)/mechanochromic luminescence behavior of a pyridyl-substituted solid-state fluorophore. The solid-state Emission Color of this pyridyl-substituted dye was systematically shifted in the bathochromic direction by forming cocrystals with several benzoic acid derivatives that exhibit different pKa values. Upon grinding these cocrystals with a spatula, further bathochromic shifts of their maximum Emission wavelengths were observed upon amorphization. Conversely, the Emission Color and crystallinity can be recovered upon heating the ground samples of the cocrystals to their cold-crystallization transition temperature (Tc ∼ 100 °C). Heating the ground cocrystals further (185–260 °C) removes the benzoic acid derivatives, which restores the original Emission Color of the pyridyl-substituted dye. In other words, we have developed a new system that exhibits a two-step Emission Color recovery in response to temperature by combining halochromic and mechanochromic luminescence in series.
Jun Yeob Lee - One of the best experts on this subject based on the ideXlab platform.
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Blue-shifted Emission Color and high quantum efficiency in solution-processed blue thermally activated delayed fluorescence organic light-emitting diodes using an intermolecular interaction suppressing host decorated with blocking groups
Journal of Materials Chemistry C, 2018Co-Authors: Sang Kyu Jeon, Hee-jun Park, Jun Yeob LeeAbstract:A high triplet energy material with the ability to suppress intermolecular interactions was synthesized as a host for a blue thermally activated delayed fluorescence (TADF) emitter for blue-shifted Emission Color and high quantum efficiency in solution-processed TADF organic light-emitting diodes. The host material, (5-(tert-butyl)-2-(4-(tert-butyl)phenoxy)phenyl)diphenylphosphine oxide (POBBPE), was designed to have a phenoxyphenyl core structure for high triplet energy, a diphenylphosphine oxide group for electron transport, and two tert-butyl units to prevent intermolecular interaction. Solution-processed blue TADF devices were developed using the POBBPE host and 2,3,4,5,6-penta(9H-carbazol-9-yl)benzonitrile (5CzCN) as the emitter, and a high quantum efficiency of 23.3% was achieved. In particular, the Color coordinates of the solution-processed POBBPE:5CzCN devices were (0.16, 0.23), which were significantly blue-shifted compared to the Color coordinates of (0.17, 0.31) from a previous 5CzCN device fabricated using a well-known bis[2-(diphenylphosphino)phenyl]ether oxide host.
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Simultaneous improvement of Emission Color, singlet–triplet energy gap, and quantum efficiency of blue thermally activated delayed fluorescent emitters using a 1-carbazolylcarbazole based donor
Chemical communications (Cambridge England), 2016Co-Authors: Mounggon Kim, Jeong Min Choi, Jun Yeob LeeAbstract:Blue thermally activated delayed fluorescent (TADF) emitters having 1-carbazolylcarbazole based donor moieties were developed to resolve the low quantum efficiency and large singlet-triplet energy splitting issues of the linker free TADF emitters. Investigation of the 1-carbazolylcarbazole derived donors as the donor units of two blue TADF emitters in comparison with 3-carbazolylcarbazole demonstrated that the 1-carbazolylcarbazole based donors increased the triplet energy, decreased the singlet-triplet energy gap, blue-shifted the Emission Color, and enhanced the quantum efficiency of the blue TADF devices.
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Emission Color management of dual emitting organic light-emitting diodes by selective switching of phosphorescence through host engineering
Journal of Industrial and Engineering Chemistry, 1Co-Authors: Ho Jin Jang, Cho Rong Kim, Jun Yeob LeeAbstract:Abstract A device approach to manage the Emission Color of the organic light-emitting diodes (OLEDs) which show two Emission processes of thermally activated delayed fluorescence (TADF) and phosphorescence was developed by engineering the host of the emitter. The emitting material was phenyl(10-phenyl-10H-phenoselenazin-3-yl)methanone (PSeBz) which emitted at 496 nm by TADF process and at 559 nm by phosphorescence process. The phosphorescence of the PSeBz emitter was selectively switched by the host because the triplet excitons can be intentionally quenched by the low triplet energy host. Therefore, the Color coordinate of the OLEDs could be tuned from (0.35, 0.52) to (0.41, 0.52) by just changing the host of the PSeBz emitter.
Takashi Kato - One of the best experts on this subject based on the ideXlab platform.
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a stimuli responsive photoluminescent anthracene based liquid crystal Emission Color determined by thermal and mechanical processes
Advanced Functional Materials, 2009Co-Authors: Yoshimitsu Sagara, Shogo Yamane, Toshiki Mutai, Koji Araki, Takashi KatoAbstract:Here, a photoluminescent liquid crystal that exhibits a change of Emission Color on the metastable–stable phase transition induced by external stimuli is prepared. A 2,6-diethynylanthracene derivative with amide groups and dendritic side chains exhibits a columnar phase on slow cooling from the isotropic phase and shows blue Emission in this columnar phase. In contrast, a cubic phase is obtained by rapid cooling from the isotropic phase. In the cubic phase, the 2,6-diethynylanthracene cores form excimers, resulting in yellow Emission. While the columnar phase is a stable liquid-crystalline (LC) phase, the cubic phase is a metastable LC phase. It is found that a change of the photoluminescent Color from yellow to blue is observed on the cubic-columnar phase transition induced by heating or mechanical shearing for this 2,6-diethynylanthracene derivative in the cubic phase. This change of photoluminescent Color is ascribed to the inhibition of excimer formation on the metastable–stable LC phase transition.
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A Stimuli‐Responsive, Photoluminescent, Anthracene‐Based Liquid Crystal: Emission Color Determined by Thermal and Mechanical Processes
Advanced Functional Materials, 2009Co-Authors: Yoshimitsu Sagara, Shogo Yamane, Toshiki Mutai, Koji Araki, Takashi KatoAbstract:Here, a photoluminescent liquid crystal that exhibits a change of Emission Color on the metastable–stable phase transition induced by external stimuli is prepared. A 2,6-diethynylanthracene derivative with amide groups and dendritic side chains exhibits a columnar phase on slow cooling from the isotropic phase and shows blue Emission in this columnar phase. In contrast, a cubic phase is obtained by rapid cooling from the isotropic phase. In the cubic phase, the 2,6-diethynylanthracene cores form excimers, resulting in yellow Emission. While the columnar phase is a stable liquid-crystalline (LC) phase, the cubic phase is a metastable LC phase. It is found that a change of the photoluminescent Color from yellow to blue is observed on the cubic-columnar phase transition induced by heating or mechanical shearing for this 2,6-diethynylanthracene derivative in the cubic phase. This change of photoluminescent Color is ascribed to the inhibition of excimer formation on the metastable–stable LC phase transition.
Soo Young Park - One of the best experts on this subject based on the ideXlab platform.
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Strategic Emission Color tuning of highly fluorescent imidazole-based excited-state intramolecular proton transfer molecules
Physical chemistry chemical physics : PCCP, 2012Co-Authors: Sanghyuk Park, Ji Eon Kwon, Soo Young ParkAbstract:Highly fluorescent molecules harnessing the excited state intramolecular proton transfer (ESIPT) process are promising for a new generation of displays and light sources because they can offer very unique and novel optoelectronic properties which are different from those of conventional fluorescent dyes. To realize innovative ESIPT devices comprising full Emission Colors over the whole visible region, a molecular design strategy for predictable Emission Color tuning should be established. Here, we have developed a general strategy for a wide-range spectral tuning of imidazole-based ESIPT materials based on three different strategies – introduction of a nodal plane model, extension of effective conjugation length, and modification of heterocyclic rings. A series of nine ESIPT molecules were designed, synthesized and comprehensively investigated for their characteristic Emission properties. All these molecules commonly showed no clear and transparent visible range absorption with no absorption Color, but showed different Colors of intense photoluminescence over broad visible regions from 450 nm (HPI) to 630 nm (HPNO) depending on their molecular structure. With the aid of density functional theory and time-dependent DFT calculations using M06, wB97XD, and B3LYP parameters with the 6-31G(d,p) basis set, these tuned Emission bands of nine emitters were assigned from the stabilized excited state conformations that were derived from modified molecular structures.