Dual Emission Properties Research Articles

Hydrogen Bond-Mediated Self-Assembly of Carbon Dots Enabling Precise Tuning of Particle and Cluster Luminescence for Advanced Optoelectronic Applications.

The effective control over the self-assembly process of carbon dots (CDs) and their cluster luminescence in the aggregated state is of paramount significance and challenge. This study, for the first time, systematically explores the photoluminescent behavior of CDs in their aggregated state, which is less understood compared to their discrete state. By investigating the effects of concentration and solvent environment, it's demonstrated that CDs could exhibit dual emission properties, shifting from blue particle emissions to red cluster emissions as they aggregate. The key to this tunable luminescence lies in hydrogen bonding, which drives the self-assembly of CDs and modulates their photo physical properties. These findings reveal that through precise control of aggregation, CDs can be engineered for advanced optoelectronic applications, including tunable light-emitting diodes (LEDs), secure information encryption, and fingerprint authentication. This report not only deepens the understanding of the underlying mechanisms governing CDs' cluster luminescence but also introduces a novel approach to exploiting their unique properties for technological innovation.

Influence of carbon dots as modifier and SiO2 shell coating as a protecting layer in YAlO3:Cr3+ phosphors for multimodal applications

This study focuses on the synthesis of SiO2-coated carbon dots (CDs) grafted onto YAlO3:Cr3+ (YAP:Cr3+) nanophosphors (NPs) through a combustion method. The CDs enhance the absorption cross-section of Cr3+ ions, significantly boosting the luminescence of YAP:Cr3+ by 19.29-fold. Further improvement is achieved with a SiO2 coating, leading to a 48.73-fold increase in photoluminescence intensity. The NCs are colour tunable, with emissions ranging from pinkish-red to blue, depending on the concentration of CDs and the excitation wavelength. These properties make them suitable for diverse applications, such as ratio metric fluorescence sensors for detecting Fe3+ ions within the 0–350 µM range, with high sensitivity (0.2 µM) and a low detection limit (4.93 μM). Additionally, they serve as material for white light-emitting diodes (W-LEDs), achieving CIE coordinates of (0.31, 0.30) and a rendering index of 94. The NCs also function as an optical thermometer with a sensitivity of 0.31 % K−1 at 320 K, making them ideal for temperature sensing applications. Moreover, their stability and dual-emissive nature make them highly effective in latent fingerprints (LFPs) detection, enabling high-resolution, level III fingerprint analysis. The dual emission properties of CDs and Cr3+ ions position these NCs as multifunctional materials, suitable for optical sensing, lighting, and security applications.

Dual-emissive carbon dots with high-color purity from sweet basil leaves: synthesis, characterization and optical properties

Abstract In this study, we synthesized dual-emission carbon dots (CDs) from sweet basil leaves dissolved in hexane using the hydrothermal method. Extensive analyses were carried out on their morphology, structure, and optical properties. The CDs show a spherical shape and highly disordered structure with an average diameter of 2 nm. They predominantly comprise carbon surrounded by a dense shell layer of oxygen and nitrogen-related functional groups. Under excitation at a single wavelength of 380 nm, the CDs emit two distinct peaks at 450 and 675 nm demonstrating a narrow bandwidth emission with full width at half maximum (FWHM) of 72 and 27 nm, respectively. The emission characteristics of the CDs are ascribed to the combined effects of radiative recombination of the carbon-core and fully passivated surface states, resulting in two distinct emission peaks and excitation-independent emission property. We present a highly effective and eco-friendly approach approach to fabricate luminescent CDs exhibiting dual emission properties derived from sustainable resources, holding promise for utilization in bioimaging.

Versatile Molecular Structure Strategy Toward Highly Efficient Single‐Component White Organic Light–Emitting Diodes

AbstractLuminophores' dual emission (DE) properties hold great potential for realizing single‐component white organic light–emitting diodes (WOLEDs). This study illustrates that the unique and vibrant DE phenomena with different luminous mechanisms can be formed through simple modulation of molecular structures. Four target luminophores, namely 2‐TPE‐PPI, 2‐TPE‐PI, 2‐TPE‐An‐PPI, and 2‐TPE‐An‐PI, capable of DE under different conditions, are intentionally designed and successfully synthesized. Owing to the inherent flexibility of the minor molecular backbone and minor steric hindrance, 2‐TPE‐PPI and 2‐TPE‐PI exhibit DE spectra in dilute solutions with different solvent polarities. The intrinsic cause of the DE phenomenon in 2‐TPE‐An‐PPI and 2‐TPE‐An‐PI arises from the localized distribution of frontier molecular orbits resulting from the presence of an anthracene unit and the formation of an exciter group through intermolecular interactions involving anthracene. Remarkably, single‐emissive‐layer WOLEDs based on 2‐TPE‐An‐PPI and 2‐TPE‐An‐PI demonstrate stable white emission with CIE coordinates at (0.33, 0.39) and (0.30, 0.39), respectively, closely approaching the CIE coordinates of standard white light. Moreover, they maintain stable EL spectra from 4 to 10 V, an exceptional attribute rarely observed in many white light devices.

Highly sensitive and selective L-lactate monitoring in complex matrices with a ratiometric fluorescent sensor RhB@Zn-MOF

L-lactate is an essential biomarker in clinical diagnostics and food quality assessment. This study introduces a novel ratiometric fluorescence sensor, RhB@Zn-MOF, which was specifically designed for the sensitive and selective detection of L-lactate. Through the strategic incorporation of Rhodamine B (RhB) into Zn-MOF, RhB@Zn-MOF was synthesized, exhibiting dual-emission properties and could effectively distinguish L-lactate in complex biological and food matrices such as milk and sweat based on the competitive absorption mechanism. Notably, the sensor achieves a low detection limit of 0.091 μM and demonstrates excellent stability and reproducibility in varied conditions. Furthermore, the integration of the sensor with smartphone technology enables rapid, real-time analysis, showcasing potential applications in sports medicine, clinical environments, and the food industry.

Regulation of TADF and RTP Dual Emission via Internal and External Heavy-Atom Effects.

Organic materials with thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP) dual emission have attracted great attention in recent years, but the regulation mechanism via internal and external heavy atoms is not clear enough. Here, we carry out a systematic theoretical investigation on the photophysical properties of the materials by introducing aliphatic or aromatic bromine atoms. The molecule with aromatic bromine atoms exhibits obvious TADF owing to the effective reverse intersystem crossing (RISC) with matchable energy levels and enhanced spin orbit couplings, the molecule with aliphatic bromine atoms shows a long RTP lifetime because of the reduced nonradiative transition of triplet excitons, and the molecule with both aliphatic and aromatic bromine atoms presents balanced TADF and RTP emissions thanks to the synergy internal and external heavy-atom effects. Besides, the internal and external heavy atoms induce multisite intermolecular interactions, effectively suppressing the nonradiative process in the solid phase. The efficient RISC process and the suppressed nonradiative process of triplet excitons should be key to regulating the dual emission property. These findings and insights are of great importance for revealing the structure-performance relationship, providing theoretical guidance for the design of TADF and RTP dual emission molecules via internal and external heavy-atom effects.

Dual-emission red carbon dots for ATP real-time monitoring and quantification to reveal drug and cancer effects on lysosomes

Monitoring and quantifying ATP levels in vivo is essential to understanding its role as a signaling molecule in tumor progression and therapy. Nevertheless, the real-time monitoring and quantitative assessment of lysosomal ATP remains challenging due to the lack of accurate tools in deep tissues. In this study, based on the crosslinking enhanced emission (CEE) effect, we successfully synthesized red carbon dots (R-CDs) with dual emission properties for efficient quantification of intracellular ATP. The R-CDs emit in the near-infrared range and target lysosomes with rapid detection capabilities, rendering them exceptionally well-suited for directly observing and analyzing the dynamics of lysosomal ATP through live cell imaging techniques. Importantly, R-CDs have proven their efficacy in real-time monitoring of drug stimulus-induced fluctuations in endogenous lysosomal ATP concentration and have also been employed for quantifying and distinguishing lysosomal ATP levels among normal and cancer cell lines. These noteworthy findings emphasize the versatility of the R-CD as a valuable imaging tool for elucidating the functional role of lysosomal ATP in drug screening and cancer diagnostics and hold the promise of becoming a reference tool for deepening our understanding of drug mechanisms of action.

A dual-emission fluorescent probe with independent polarity and viscosity responses: The synthesis, spectroscopy and bio-imaging applications

Viscosity and polarity are essential parameters that play critical roles in various physiological processes. Thus, dual-emission fluorescent probes that respond to both polarity and viscosity are highly sought-after tools for studying these processes. In addressing this need, a novel fluorescent probe (L), with dual emissions centered at 460 nm and 780 nm, which can sensitively respond to polarity and viscosity respectively, has been developed. Probe (L) is constructed through rational molecular design, utilizing two conjugated synthons connected by a π-bond to form a D-π-A system. The twisted intramolecular charge transfer (TICT) state is dominant in low-viscosity environments, resulting in weak near-infrared (NIR) fluorescence. Conversely, the intramolecular charge transfer (ICT) state is expected to prevail in high-viscosity environments, leading to strong NIR fluorescence. The polarity-sensitive fluorescence centered at 460 nm can be attributed to the emission of the coumarin unit. Moreover, probe (L) exhibits low cytotoxicity and primarily targets mitochondria. By leveraging the dual-emission properties of probe (L), real-time imaging of polarity and viscosity fluctuations within cells has been achieved. Additionally, probe (L) can be used for in situ and in vivo imaging of rheumatoid arthritis (RA) with good imaging resolution.

A single-component sensor array to detect multiple antibiotics via dual-emission chlorophyll carbon dots

In this study, dual-emission carbon dots (DE-CDs) were fabricated using a straightforward one-step hydrothermal synthesis with natural chlorophyll as the carbon precursor. These DE-CDs not only preserve the porphyrin structure of chlorophyll, exhibiting notable fluorescence at 682 nm, but they also display the characteristic fluorescence emission of conventional CDs at 450 nm. Leveraging the unique dual-emission properties of DE-CDs, we have engineered a single-component fluorescent sensor array for the high-throughput detection of antibiotics, which are emerging contaminants in water. The fluorescence responses (F450, F682, and the F450/F682 ratio) of the DE-CDs toward various antibiotics were analyzed using principal component analysis (PCA), enabling the facile differentiation of multiple antibiotics with good reproducibility achieved in real water samples. This innovative DE-CDs approach eliminates the need for multiple sensing probes and offers a practical concept for the creation of single-component sensing platforms.

Ultrafast excited state intramolecular proton transfer and isomerization of long-chain linked Schiff bases.

The ultrafast proton transfer and the following dynamics for aromatic Schiff bases N,N'-bis(salicylidene)ethylenediamine (salen) and N,N'-bis(salicylidene)-1,4-butylenediamine (salbn) were investigated with experimental and theoretical methods. A dual emission property with a large Stokes shift in salen and salbn indicates that excited state intramolecular proton transfer occurs with photoexcitation. An efficient single proton transfer was confirmed within 200fs for both molecules. Subsequently, a fast twisted motion of the keto moiety carries cis-keto to a relaxed stable geometry in the S1 state. Following the twisted motion, the phenol ring at keto moiety further rotates to a conical intersection with the ground state and a cis-trans isomerization occurs. The isomerization rate is high, which dominates the competition with the radiative transition, resulting in weak emission intensity. It is confirmed that the length of alkyl chain affects the direction of phenol ring twisting and rotation during the whole subsequent relaxation of excited cis-keto tautomer. Compared with polar solvent acetonitrile, the barrier of isomerization is higher and the hydrogen bond on keto moiety is stronger in nonpolar solvent toluene. It makes fluorescence radiation channels competing with isomerism more likely to occur, contributing to the observed difference of enol/keto emission ratios of salen and salbn in toluene and acetonitrile.

A NIR-Fluorochrome for Live Cell Dual Emission and Lifetime Tracking from the First Plasma Membrane Interaction to Subcellular and Extracellular Locales.

Molecular probes with the ability to differentiate between subcellular variations in acidity levels remain important for the investigation of dynamic cellular processes and functions. In this context, a series of cyclic peptide and PEG bio-conjugated dual near-infrared emissive BF2-azadipyrromethene fluorophores with maxima emissions at 720 nm (at pH > 6) and 790 nm (at pH < 5) have been developed and their aqueous solution photophysical properties determined. Their inter-converting emissions and fluorescence lifetime characteristics were exploited to track their spatial and temporal progression from first contact with the plasma membrane to subcellular locales to their release within extracellular vesicles. A pH-dependent reversible phenolate/phenol interconversion on the fluorophore controlled the dynamic changes in dual emission responses and corresponding lifetime changes. Live-cell confocal microscopy experiments in the metastatic breast cancer cell line MDA-MB-231 confirmed the usability of the dual emissive properties for imaging over prolonged periods. All three derivatives performed as probes capable of real-time continuous imaging of fundamental cellular processes such as plasma membrane interaction, tracking endocytosis, lysosomal/large acidic vesicle accumulation, and efflux within extracellular vesicles without perturbing cellular function. Furthermore, fluorescence lifetime imaging microscopy provided valuable insights regarding fluorophore progression through intracellular microenvironments over time. Overall, the unique photophysical properties of these fluorophores show excellent potential for their use as information-rich probes.

Visualization of salt diffusion in beef curing process using Smartphone-Assisted ratiometric fluorescent sensor

Herein, a smartphone-assisted fluorescent sensor was proposed for real-time fluorescence imaging and monitoring of salt diffusion in beef curing process. The glutathione modified carbon quantum dots @ curcumin (CQDs@CCM) probe with dual-emissive properties was prepared using natural biomass materials. In the probe, the CQDs with blue fluorescence was quenched by CCM due to the inner filter effect (IFE). When the probe was exposed to highly saturated sodium salt, CCM formed a complex with sodium ions, interrupting the IFE behavior and resulting in the fluorescence recovery of CQDs. Significantly, the innovative application of CCM in curing scenarios effectively circumvents the interference of other metal ions. To our knowledge, this is the first report to apply smartphone-assisted fluorescent sensor to salt imaging of cured beef. Notably, the finite element analysis was performed to simulate the diffusion of salt in beef using COMSOL, and the simulation showed similar results to fluorescence analysis, indicating the established visualizing method and the simulated model can provide effective information for beef marination process. This study provide technical support for precise control of the beef curing degree and offer new insights into the fluorescence imaging in food flavor monitoring.

Engineering Tunable Ratiometric Dual Emission in Single Emitter-based Amorphous Systems.

Molecular emitters with multi-emissive properties are in high demand in numerous fields, while these properties basically depend on specific molecular conformation and packing. For amorphous systems, special molecular arrangement is unnecessary, but it remains challenging to achieve such luminescent behaviors. Herein, we present a general strategy that takes advantage of molecular rigidity and S1 -T1 energy gap balance for emitter design, which enables fluorescence-phosphorescence dual-emission properties in various solid forms, whether crystalline or amorphous. Subsequently, the amorphism of the emitters based polymethyl methacrylate films endowed an in situ regulation of the dual-emissive characteristics. With the ratiometric regulation of phosphorescence by external stimuli and stable fluorescence as internal reference, highly controllable luminescent color tuning (yellow to blue including white emission) was achieved. There properties together with a persistent luminous behavior is of benefit for an irreplaceable set of optical information combination, featuring an ultrahigh-security anti-counterfeiting ability. Our research introduces a concept of eliminating the crystal-form and molecular-conformational dependence of complex luminescent properties through emitter molecular design. This has profound implications for the development of functional materials.

Tunable multimode emission induced by charge transfer and multiple resonance effect

Single-component luminescent materials with dual emission properties show great promise in material and life science. Here, we report a novel thermally activated delayed fluorescence (TADF) emitter BO-PST based on a rigid B-embedded dioxygen-bridged acceptor (A) and flexible phenothiazine donor (D). The flexibility of D unit contributes to different charge transfer characteristic and interesting multimode emission in various environment, including D-A-type TADF emission, multi-resonant (MR) fluorescence emission and MR induced afterglow with long lifetime of 1.55 s. Single-crystal structures and theoretical calculations prove that dual emission originates from the quasi-equatorial and quasi-axial conformers of the phenothiazine unit, respectively. The dynamic multicolor properties demonstrate the potential of the novel BO-PST molecule in the volatile organic compounds (VOCs) detection and the stimulus-responsive application.

Ratiometric Electrochemiluminescence of Zirconium Metal-Organic Framework as a Single Luminophore for Sensitive Detection of HPV-16 DNA.

This study developed a new zirconium metal-organic framework (MOF) luminophore named Zr-DPA@TCPP with dual-emission electrochemiluminescence (ECL) characteristics at a resolved potential. First, Zr-DPA@TCPP with a core-shell structure was effectively synthesized through the self-assembly of 9,10-di(p-carboxyphenyl)anthracene (DPA) and 5,10,15,20-tetra(4-carboxyphenyl)porphyrin (TCPP) as the respective organic ligands and the Zr cluster as the metal node. The reasonable integration of the two organic ligands DPA and TCPP with ECL properties into a single monomer, Zr-DPA@TCPP, successfully exhibited synchronous anodic and cathodic ECL signals. Besides, due to the impressively unique property of ferrocene (Fc), which can quench the anodic ECL but cannot affect the cathodic ECL signal, the ratiometric ECL biosensor was cleverly designed by using the cathode signal as an internal reference. Thus, combined with DNA recycle amplification reactions, the ECL biosensor realized sensitive ratiometric detection of HPV-16 DNA with the linear range of 1 fM-100 pM and the limit of detection (LOD) of 596 aM. The distinctive dual-emission properties of Zr-DPA@TCPP provided a new idea for the development of ECL luminophores and opened up an innovative avenue of fabricating the ratiometric ECL platform.

Solvent- and pH-Stable Eu(III)-Based Metal-Organic Framework with Phosphate-Ratio Fluorescence Sensing and Significant Proton Conduction.

Lanthanide-based metal-organic frameworks show good potential for applications due to their unique structures and functional properties. A highly thermally and acid-base stable Eu-MOF was synthesized by a solvothermal method with the molecular formula {[(CH3)2NH2]2[Eu2(NDDP)2(H2O)2]·H2O}n (Eu-MOF, H4NDDP = 5,5'-(naphthalene-2,6-diyl)diisophthalic acid). Eu-MOF takes a three-dimensional (4,4,8)-connected topology. The water molecules involved in the coordination, free water molecules, and [(CH3)2NH2]+ cations in the pore can be used as proton carriers. The proton conductivity attains 1.25 × 10-4 S cm-1 at room temperature and 2.42 × 10-3 S cm-1 at 70 °C and 98% relative humidity. Combined with the dual-emission properties from the ligands and Eu(III) ions enables Eu-MOF to be used as a ratiometric fluorescent sensor for phosphate efficiently and rapidly, with a limit of detection of 0.12 μM in the Tris-HCl buffer solution. These results provide a new approach for the construction of MOFs with high proton conductivity and a ratiometric fluorescence response.

Intrinsic self-calibration electrostatic-controlled ratiometric fluorescence assay of histamine in human serum and canned tuna fish samples

Bimetallic nanoclusters protected by proteins have gained significant attention in the sensing field due to their aggregation-induced emission (AIE) property. However, their applications may be restricted by the effects of temperature, pH, ethanol, and metal ions. Therefore, the development of self-assembling technology could increase the potential applications of these materials. In this study, positively charged silicon nanoparticles (SiNPs) were mixed with negatively charged bovine serum albumin-protected silver doped gold nanoclusters (BSA@AgAuNCs) through an electrostatic interaction. The resulting system exhibited dual emissions at 610 nm ((BSA@AgAuNCs) and 460 nm (SiNPs) when excited at 370 nm. The mixing of SiNPs led to an increase in the fluorescence emission of BSA@AgAuNCs due to an aggregation-induced emission (AIE) enhancement. However, the addition of histamine, which is positively charged at pH 5.5, caused the SiNPs to be triggered and adsorbed onto the surface of BSA@AgAuNCs, resulting in their disaggregation and a decrease in their fluorescence emission. Simultaneously, the blue fluorescence emission of SiNPs at 460 nm was not affected and remained unchanged. Under optimized conditions, the fluorescence response (F460/F610) showed a linear increase with the concentration of histamine in the range of 0.01–80 µM, with a detection limit (S/N = 3) of 3.0 nM. The probe demonstrated excellent sensitivity, selectivity, and reliability in quantifying histamine in complex matrices. The recoveries % values are in the range of 97–102% and 97.7–104.4% with RSD % in the range of 2.67–3.98% and 2.78–4.00% for human blood serum and canned tuna fish samples, respectively. This work presents new opportunities for the development of sensors based on self-assembling and dual emissive properties for (bio) sensing applications.

In-Situ Temporal Characterization of Chirped Ultra-Broadband Laser Pulses Exciting a Dual-Light Emitter Er3+-Doped Perovskite

We take advantage of the dual emission properties of up-conversion fluorescence (UCF) and second harmonic generation (SHG) in Er3+-doped perovskite Na0.95Er0.05Nb0.9Ti0.1O3 to fully temporally characterize the ultrashort laser pulse that excites Er3+-ion fluorescence. The chirped pulses from a broadband Ti:Sa oscillator are temporally characterized using the dispersion scan (d-scan) technique by using the SHG signal in the host perovskite at the same point where UCF is being produced by the same pulse. The pulse durations obtained range from ~45 fs to ~8 fs and positive and negative spectral phases are unambiguously identified. The temporal characterization is compared using a standard non-linear crystal and perfect agreement is obtained. These results show that it is possible to temporally characterize in-situ ultrashort laser pulses while they are inducing a UCF process, as long as the host generates second-harmonic signal.

Zinc(II)-Based Ring-and-Rod Coordination Layer as an Excitation-Wavelength-dependent Dual-Emissive Chemosensor for Discriminating Fe3+, Cr3+, and Al3+ in Water.

The reactions of Zn(NO3)2, 3,6-bis(pyridin-3-yl)-9H-carbazole (bpycz), and 2,5-dihydroxyterephthalic acid (H4dhbdc) or 2-bromoterephthalic acid (Br-1,4-H2bdc) under hydro(solvo)thermal conditions yielded corresponding coordination polymers (CPs) {[Zn(H2dhbdc)(bpycz)]•0.5H2O}n (1) and [Zn(Br-1,4-bdc)(bpycz)]•2DMAc•H2O (2), respectively, with high thermal stability approaching 350 °C. CP 1 adopts a ring-and-rod layer structure, which is topologically described as a 4-connected net with the point symbol of 2•65. Two layers are interpenetrated in parallel interlocking mode to form a double 2D → 2D polyrotaxane entanglement with extra-framework void space of 19.6%. CP 2 has a non-interpenetrating ring-and-rod layer structure of 4-connected 2•65 net topology, with extra-framework void space of 16.6%. Thermally activated 1 and 2 revealed CO2 uptakes of 101.1 and 98.6 cm3 g-1, respectively, at P/P0 = 1 and 195 K. X-ray powder diffraction (XRPD) patterns confirmed that 1 and 2 both possessed high chemical stability in H2O, CH3OH, acetone, and DMF, and framework stability during gas adsorption-desorption. The H2O suspension of 1 displayed excitation-dependent dual-emissive properties, appearing at 432 nm upon excitation at 300 nm and at 528 nm upon excitation at 365 nm. Of note, 1 was capable of detection of Fe3+, Cr3+, and Al3+ ions in H2O, showing good anti-interference ability, excellent selectivity, and high sensitivity. More interesting, the dual-emissive properties make 1 to be an excellent luminescence chemosensor to screen Fe3+, Cr3+, and Al3+ from a pool of metal ions in H2O upon excitation at 300 nm via luminescence quenching effect and then discriminate Fe3+, Cr3+, and Al3+ upon excitation at 365 nm via luminescence quenching, unaltered, and enhancement responses, respectively. On the other hand, the H2O suspension of 2 demonstrated an excitation-independent emission appearing at around 430 nm, which could be utilized to sensitively detect Fe3+ and Cr3+ ions with good anti-interference ability and excellent selectivity via luminescence quenching effect. Further, 1 and 2 were recyclability and possessed cycling stability. The plausible sensing mechanisms for 1 and 2 toward Fe3+, Cr3+, and Al3+ were also explored in detail.

Direction Switching and Self-Recovering Mechanochromic Luminescence of Anthracene-Modified o-Carboranes.

Luminochromic behaviors regarding mechanochromic luminescence (MCL) of o-carborane-modified anthracene derivatives are reported. We have previously synthesized bis-o-carborane-substituted anthracene and found that its crystal polymorphs show dual-emission properties composed of excimer and charge transfer (CT) emission bands in the solid state. Initially, we observed the bathochromic MCL behavior from 1 a originating from emission mechanism alteration from dual emission to CT emission. By inserting the ethynylene spacers between anthracene and o-carboranes, compound 2 was obtained. Interestingly, 2 showed hypsochromic MCL originating from the emission mechanism alteration from CT to excimer emission. Furthermore, luminescent color of ground 1 a can be recovered to the initial state by allowing to stand at room temperature, meaning that self-recovery proceeds. Detailed analyses are described in this study.