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Summary: This research delved into the role of gluten fractions on digestion, physical properties and structure of wheat starch (WS)–lauric acid (LA) system under non‐alkaline/alkaline conditions. Results showed that gluten fractions decreased the digestion of WS with LA and gliadin had greater effect on the digestion of WS with LA under non‐alkaline/alkaline conditions than glutenin. Specifically, gliadin increased RS content of WS with LA by 70.99% and 84.89%, respectively, under non‐alkaline and alkaline conditions. The diminished in WS digestion caused by gluten fractions and LA ascribed to the decrease in swelling power and leaching of starch. Rapid viscosity analyser (RVA) demonstrated that gluten fractions were conducive to WS–LA and/or WS–LA–protein complexes formation and gliadin was more helpful to these complexes' formation than glutenin under non‐alkaline conditions. Additionally, gliadin had greater effect on the stability and short‐range ordered structure of WS with LA than glutenin. Addition of gliadin resulted in 6.79% and 13.33% of increase in short‐range orderliness compared with WS–LA system under non‐alkaline and alkaline conditions, respectively. Furthermore, gluten fractions had greater influence on the digestion of WS with LA under alkaline conditions than non‐alkaline conditions ascribed to the formation of WS–LA and/or WS–LA–protein complexes with low swelling power and high ordered structure under alkaline conditions. This study provided crucial information on the design of starchy foods with low digestion. [ABSTRACT FROM AUTHOR]

Organic single crystals with near‐infrared (NIR) emission demonstrate their excellent optical communications from well photonic confinement and low optical waveguide loss, which are considered as competitive candidates toward advanced optoelectronics. However, the increasingly diverse and sophisticated application demands result in the complicated design of NIR devices, which is hardly realized solely by the intrinsic properties of individual crystals. Herein, a programmable assembly strategy is presented to fabricate organic heterostructures. Triphenylene (TP), pyrene (Py) and 7,7,8,8‐tetracyanoquinodimethane (TCNQ) are primary selected to prepared organic cocrystals with narrow band gap and near‐infrared emission. Importantly, the charge‐transfer alloy with tunable emission from 700 nm to 850 nm and branched heterostructures with multichannel characteristics are prepared from these organic cocrystals by following the growth kinetics process at molecular level and lattice matching principle at structural level, respectively. Theses prepared heterostructures exhibit optical logic operation capabilities, which can serve as optical modulators. This work provides new insights into the manufacturing of organic NIR heterostructures applied in advanced optoelectronics. [ABSTRACT FROM AUTHOR]

Objective: The temporomandibular joint (TMJ) disc cushions intraarticular stress during mandibular movements. While mechanical overloading is related to cartilage degeneration, the pathogenesis of TMJ disc degeneration is unclear. Here, we determined the regulatory role of mechanoinductive transient receptor potential vanilloid 4 (TRPV4) in mechanical overload‐induced TMJ disc degeneration. Methods: We explored the effect of mechanical overload on the TMJ discs in a rat occlusal interference model in vivo, and by applying sustained compressive force in vitro. TRPV4 inhibition was delivered by small interfering RNA or GSK2193874; TRPV4 activation was delivered by GSK1016790A. The protective effect of TRPV4 inhibition was validated in the rat occlusal interference model. Results: Occlusal interference induced TMJ disc degeneration with enhanced extracellular matrix degradation in vivo and mechanical overload promoted inflammatory responses in the TMJ disc cells via Ca2+ influx with significantly upregulated TRPV4. TRPV4 inhibition reversed mechanical overload‐induced inflammatory responses; TRPV4 activation simulated mechanical overload‐induced inflammatory responses. Moreover, TRPV4 inhibition alleviated TMJ disc degeneration in the rat occlusal interference model. Conclusion: Our findings suggest TRPV4 plays a pivotal role in the pathogenesis of mechanical overload‐induced TMJ disc degeneration and may be a promising target for the treatment of degenerative changes of the TMJ disc. [ABSTRACT FROM AUTHOR]

Organic heterostructures (OHTs) with the desired geometry organization on micro/nanoscale have undergone rapid progress in nanoscience and nanotechnology. However, it is a significant challenge to elucidate the epitaxial-growth process for various OHTs composed of organic units with a lattice mismatching ratio of > 3%, which is unimaginable for inorganic heterostructures. Herein, we have demonstrated a vivid visualization of the morphology evolution of epitaxial-growth based on a doped interfacial-layer, which facilitates the comprehensive understanding of the hierarchical self-assembly of core-shell OHT with precise spatial configuration. Significantly, the barcoded OHT with periodic shells obviously illustrate the shell epitaxial-growth from tips to center parts along the seeded rods for forming the core-shell OHT. Furthermore, the diameter, length, and number of periodic shells were modulated by finely tuning the stoichiometric ratio, crystalline time, and temperature, respectively. This epitaxial-growth process could be generalized to organic systems with facile chemical/structural compatibility for forming the desired OHTs.Organic heterostructures with controlled geometry on the micro and nanoscale are important in nanotechnology, but epitaxial growth processes with high lattice mismatching are challenging to achieve. Here, the authors report a visualisation process for morphology evolution on epitaxial growth. [ABSTRACT FROM AUTHOR]

In past decades, organic crystals have presented considerable potential in the field of optoelectronics due to their rich tunable physical and chemical properties and excellent optoelectronic characteristics. White‐light emission, as a special application, has received widespread attention and has been applied in various fields, generating significant interest in the scientific community. By preparing white light‐emitting organic crystals, a series of applications for future white‐light sources can be realized. This article reviews the research progress on the molecular design and synthesis, preparation, and application of white light‐emitting organic crystals in recent years. We hope that this review will help to understand and facilitate the development of white light‐emitting organic crystals. [ABSTRACT FROM AUTHOR]

Using phosphotungstic acid, tetraethyl ethylenebisphosphonate (L) and rare earth chloride as raw materials, a series of Keggin-type POM-based rare earth complexes were synthesized by a heating and stirring method: [LnL3(H2O)]PW12O40·CH3CN (1–6) (Ln = Dy, Ho, Er, Tm, Yb, Lu). The molecular structures of the complexes were determined by X-ray single-crystal diffraction, and the influence of weak forces on the molecular packing structures were studied by calculating the presence of hydrogen bonds inside the complexes using PLATON. By analyzing the experimental results, it is concluded that tetraethyl ethylenebisphosphonate is coordinated with rare earth ions through bidentate chelation, and POMs which are not involved in coordination exist as anions. Complexes 1–6 are three-dimensional supramolecular structures constructed by hydrogen bonds. Powder X-ray diffraction proved that the structures of the synthesized complexes are consistent with the results of single-crystal analysis, and the purity is high. Thermogravimetric analysis showed that the series of complexes have good thermal stability above 200 °C. Notably, the complexes 1–6 showed good photocatalytic degradation ability to methyl orange (MO) solution under UV irradiation; their degradation rate reached more than 95% within 15 min. The membrane material of complex 1 was successfully prepared by combining complex 1 with polyvinylidene fluoride (PVDF). Scanning electron microscopy (SEM) showed that complex 1 was supported on the surface of the PVDF film. For photocatalytic degradation of MO solution, the MO degradation rate reached 97.4% within 50 min. Compared with the powder-type catalyst, the degradation efficiency is lower, but the membrane material catalysis solves the problem of catalyst recovery and has better recyclable performance. Using the method of adding different active species scavengers, the mechanism of the photocatalytic reaction was studied. Finally, terahertz time-domain spectroscopy (THz-TDS) was performed, which provided a spectroscopic basis for the rapid detection of the weak forces contained in the complexes. [ABSTRACT FROM AUTHOR]

To examine the effects of hypokalemia on the prognosis of older adult patients with atrial fibrillation (AF).Methods: We enrolled 794 older adult patients ≥ 75 years suffering from AF, and divided them into two groups according to the inclusion and exclusion criteria: Group 1, (hypokalemia group), 246 cases, serum K+< 3.5 mmol/L; Group 2, (normal blood potassium group), 548 cases, 3.5mmol/L≤serum K+< 5.5 mmol/L. The two groups of patients were followed for 70 months to observe the occurrence of clinical events. The primary endpoint was cardiovascular death and the secondary endpoint was all-cause death.Results: The median follow-up time was 15.00 months. In terms of baseline profile characteristics, serum creatinine levels were significantly lower in Group 1 than in Group 2 patients (P=0.002). In terms of the relationship between hypokalemia and clinical outcomes, Kaplan-Meier survival analysis revealed that the incidence of clinical primary endpoint in Group 1 was significantly higher than that in Group 2 (P < 0.001), and the incidence of the secondary endpoint did not differ significantly between the two groups (P 005). Based on multivariate Cox regression risk model analysis, coronary heart disease, hemoglobin content, serum uric acid and usage of anticoagulant drugs were the independent variables related to the primary endpoint of cardiovascular death (all P< 0.01).Conclusion: The incidence of hypokalemia in older adult patients with AF was 30.98%. Hypokalemia was closely related to the cardiovascular death, and coronary heart disease, hemoglobin content, serum uric acid level, and usage of anticoagulant drugs were the independent risk factors for the primary endpoint event. [ABSTRACT FROM AUTHOR]

In this paper, three new donor–acceptor complex forms (zBC) containing a helical‐shape dibenzocarbazole analog (DBCz) as the electron donor and 1,2,4,5‐tetracyanobenzene (TCNB) as the electron acceptor via a simple solution‐processing strategy are reported. The beginning components self‐assembled into supramolecular frameworks with glamorous alignment modes and different molar ratios: ≈1:1 P or M‐enantiomer for α‐cocrystal, alternated P/M‐column stacking in mesmeric 2:3 β‐cocrystal, and segregated stacking of γ‐cocrystal. As a result, α‐cocrystal exhibits bright solid‐state red fluorescent, β‐cocrystal shows significant optical waveguide behavior with a low optical loss coefficient of ≈0.018 dB µm−1, and no visual light emission is observed for γ‐cocrystal under ultraviolet radiation. Interestingly, the α‐zBC crystal is not only emissive but also chiroptically active with dissymmetry factor (glum) of 0.004. This study on chiral stacking tailoring paves a way for functional design of organic charge‐transfer complex toward application in high‐performance organic optoelectronics. [ABSTRACT FROM AUTHOR]

Modern organic photonics is heavily reliant on micro‐/nanostructured organic crystalline materials, not least because they exhibit advantageous physicochemical properties and can be easily fabricated by bottom‐up approaches such as self‐assembly driven by weak noncovalent intermolecular interactions (van der Waals forces, π–π interactions, hydrogen bonds, halogen bonds, charge transfer interactions, etc.). Herein, the effects of these interactions on organic crystal nucleation are summarized, the resulting low‐dimensional organic crystal structures and their optoelectronic applications are discussed, and future development prospects are presented to inspire the further investigation of such optofunctional structures. [ABSTRACT FROM AUTHOR]

Near‐infrared (NIR) micro/nanolasers hold great potential for integration of optoelectronic circuitry, medical diagnosis, sensing, and so forth. For the laser medium, organic gain molecules are highly attractive in NIR micro/nanolasers due to the inherent merits of abundant excited‐state processes, chemical tunability, and solution processing. Herein, the recent advances of NIR organic micro/nanolasers on nondoped molecule aggregates are reviewed from the aspects of gain materials, fabrication of self‐assembled microcavities, and NIR lasing actions, as well as some typical examples in applications, supporting the effective construction of internal quantitative relationship of gain molecular structures, excited‐state gain processes, self‐assembled micro/nanostructures, and NIR lasing performance. Finally, conclusion and outlook are given, aiming at offering valuable revelation for further development of high‐performance NIR organic micro/nanolasers. [ABSTRACT FROM AUTHOR]

Precise fabrication of organic micro/nanostructures with regular morphology has gained a considerable concern in developing high‐performance optoelectronic devices, which is still a huge challenge to realize tunable morphology without the dependence on molecule packing arrangement. Herein, a thermodynamic/kinetic controlled self‐assembly for triphenylene‐7,7,8,8‐tetracyanoquinodimethane (TP‐TCNQ) cocrystal, with well‐defined microwires and microplates based on the same crystal structure, is proposed. With the low solution concentration of C = 5 mm, the comparable growth rates along [011] driven by π–π interaction and along [100] driven by charge‐transfer (CT) interaction facilitate the formation of thermodynamically favored shape of microplates. In contrast, the prominent CT interaction along [100] leads to the construction of microwires at kinetic state under high‐concentration solution of C = 10 mm. Furthermore, the prepared TP‐TCNQ microwires and microplates demonstrate isotropic photonic transmissions with the low optical loss coefficient of 0.033 and 0.042 dB µm−1, respectively. This strategy provides a novel avenue to finely construct the organic microcrystals with desired morphology for potential optoelectronics. [ABSTRACT FROM AUTHOR]

Organic donor–acceptor (D–A) cocrystals have recently attracted widespread attention owing to the synergetic electron donor–acceptor blending properties via non-covalent interactions, becoming good candidate materials for optoelectronic applications. However, the rational design and selection of donor/acceptor components in organic cocrystals with the desired morphology, size, and function remains a key synthetic objective. As the single components possess inherent individual properties, including optical, electronic, and crystalline lattice features, co-crystalline engineering is a powerful but challenging strategy for obtaining new materials with combined physical and chemical properties. In this review, we mainly focus on the organic donor acceptor cocrystal molecular design, synthetic approaches, and their photophysical and photochemical properties as well as optical function application devices. Finally, an outlook is provided for the future development of organic D–A cocrystals toward next-generation organic crystal materials. [ABSTRACT FROM AUTHOR]

Geometrically well-defined microcrystals with polymorphic tailorability are in high demand for multi-directional photon flow at the microscale. Herein, diphenylamine (DPA) substituted 5,6,12,13-tetraazaperopyrene c-TAPP-DPA is synthesized and explored as a versatile fluorophore to fabricate polymorphic microcrystals for photonic applications. The flexibly twisted and electron rich DPA groups are verified as a crucial structure element to tune the intermolecular interactions and packing modes of c-TAPP-DPA, resulting in three kinds of crystals, including microrods, and rhomboid and hexagonal microplates. These microcrystals display geometry-dependent fluorescence properties and 1D or 2D waveguide properties with low optical loss. Impressively, the micro-rhomboids show a unique 2D asymmetric waveguide character. Our work enriches the diversity of polymorphic microcrystals, and sheds more light on the structure–property relationship of organic crystals for multi-directional optical waveguide applications. [ABSTRACT FROM AUTHOR]

Organic semiconductor molecules possess chemical tunability and large stimulated emission cross section, representing a promising candidate for laser gain medium. However, for the pursuit of telecom‐wavelength organic lasers, one of the major obstacles is the lack of effective energy‐level systems with high optical gain to compensate the exciton deactivation losses. Herein, the effects of molecular conformation‐dependent distinct cascaded proton‐transfer six‐level energy gain systems on lasing emission properties are systematically investigated based on organic polymorphs, proving that an energy‐level gain system without reversible transition channels is more conducive to the formation of efficient population inversion and high optical gain. Notably, the one‐way irreversible six‐level energy system of β‐phase polymorph supports more favorable population inversions than the two‐way reversible six‐level system of α‐phase polymorph due to the irreversible excited‐state second proton transfer and the irreversible ground‐state recovery, achieving the amplified spontaneous emission at telecom‐wavelength of ≈850 nm. This study provides useful guidelines for constructing efficient energy‐level gain systems, promoting the exploration of high‐gain organic semiconductor laser materials from visible to near‐infrared region. [ABSTRACT FROM AUTHOR]

The combination of multiple components or structures into integrated micro/nanostructures for practical application has been pursued for many years. Herein, a series of hierarchical organic microwires with branch, core/shell (C/S), and branch C/S structures are successfully constructed based on organic charge transfer (CT) cocrystals with structural similarity and physicochemical tunability. By regulating the intermolecular CT interaction, single microwires and branch microstructures can be integrated into the C/S and branch C/S structures, respectively. Significantly, the integrated branch C/S microwires, with multicolor waveguide behavior and branch structure multichannel waveguide output characteristics, can function as an optical logic gate with multiple encoding features. This work provides useful insights for creating completely new types of organic microstructures for integrated optoelectronics. [ABSTRACT FROM AUTHOR]

The combination of multiple components or structures into integrated micro/nanostructures for practical application has been pursued for many years. Herein, a series of hierarchical organic microwires with branch, core/shell (C/S), and branch C/S structures are successfully constructed based on organic charge transfer (CT) cocrystals with structural similarity and physicochemical tunability. By regulating the intermolecular CT interaction, single microwires and branch microstructures can be integrated into the C/S and branch C/S structures, respectively. Significantly, the integrated branch C/S microwires, with multicolor waveguide behavior and branch structure multichannel waveguide output characteristics, can function as an optical logic gate with multiple encoding features. This work provides useful insights for creating completely new types of organic microstructures for integrated optoelectronics. [ABSTRACT FROM AUTHOR]

Pot and field trials were conducted to investigate Cd uptake and phytoremediation efficiency of two Brassica napus cultivars (QY-1 and SYH) with applied water-soluble chitosan (WSC, Pot: 0, 2% and 4%; Field: 0 and 10 g·m−2) grown in Cd-contaminated soils. The results from the pot and field trials generally showed that WSC treatments significantly increased Cd concentrations in shoot and root tissues by 33.77–159.71% (except for SYH/JY) and 7.42–168.71% of two B. napus cultivars compared with the control (p < 0.05). The uptake of Cd by shoots of SYH was obviously higher than by shoots of QY-1 treated with WSC under pot and field conditions, which was 1.54–2.22 times than that of QY-1 (p < 0.05). The results indicated that 2% WSC treatment significantly increased the water-soluble and acid extractable Cd in rhizosphere soils of both B. napus cultivars. Furthermore, Cd concentrations in the oils of two B. napus cultivars with applied WSC (10 g·m−2) grown under field conditions were not significantly different from commercial rapeseed oils. Rapeseed oil of B. napus is not only an edible oil with high nutritional value, but it can also be converted into biomass diesel that can be used as a substitute for petroleum diesel. [ABSTRACT FROM AUTHOR]

Vapor‐phase growth methods, taking the advantages of producing high‐quality crystals with low defects, thin thickness, and homogeneous composition, are of great significance in the field of organic crystal growth and their high‐performance applications. At present, the requirements for organic crystals as building blocks for the construction of optoelectronic devices are increasing with the constant advances in organic optoelectronics. Therefore, the vapor‐phase growth method would become one of the practical techniques that cannot be ignored to fabricate organic crystals. In this paper, an overview of different vapor‐phase growth methods for the preparation of organic single crystals is provided. An introduction to the current status of the vapor phase method is presented and the view on the challenges it faces with some promising solution ideas. It is believed that this review will serve as a reference for further development and an inspiration for the new way forward. [ABSTRACT FROM AUTHOR]

Organic gain materials, with the merit of abundant excited‐state processes with large stimulated emission cross‐section, show considerable potential in lasers. The abundant excited‐state processes provide excellent platform for the construction of various forms of energy‐level systems, based on which the efficient population inversion and the tailorable gain region are supported. Herein, the development of organic lasers with distinctive energy‐level systems is summarized according to the classification of excited‐state gain processes including singlet quasi‐four‐level transition, energy transfer, excimer, charge transfer (CT), excited‐state intramolecular proton transfer (ESIPT), and some other novel photophysical processes, giving deep insight into the inherent relationship between energy‐level systems and laser action. Finally, the challenges and perspectives for the future development are presented, hopefully to offer valuable enlightenment for the further optimization of energy‐level systems toward high‐gain organic lasers including electrically pumped organic lasers. [ABSTRACT FROM AUTHOR]

Organic molecules which can undergo excited‐state intramolecular proton transfer (ESIPT) process have been considered as ideal gain materials for near‐infrared organic lasers owing to their effective four‐level systems. However, extending lasing wavelength beyond 800 nm with present ESIPT‐active gain materials is still in challenge. Herein, we established a molecular design strategy that operates via extending the π‐conjugated system of the ESIPT parent core to enhance the cascaded double ESIPT process and thus to achieve the red‐shifted six‐level system lasing. Concretely, a model molecule with 1,9‐dihydroxyanthracene as the ESIPT parent core was designed and synthesized, which was proved to undergo twice cascaded ESIPT processes while the 1,8‐dihydroxynaphthalene‐based analogue can only undergo once ESIPT process based on DFT calculations and ultrafast dynamics analyses. Finally, a six‐level system lasing toward 900 nm was achieved with a low threshold of 27.4 μJ cm−2. [ABSTRACT FROM AUTHOR]

Organic molecules which can undergo excited‐state intramolecular proton transfer (ESIPT) process have been considered as ideal gain materials for near‐infrared organic lasers owing to their effective four‐level systems. However, extending lasing wavelength beyond 800 nm with present ESIPT‐active gain materials is still in challenge. Herein, we established a molecular design strategy that operates via extending the π‐conjugated system of the ESIPT parent core to enhance the cascaded double ESIPT process and thus to achieve the red‐shifted six‐level system lasing. Concretely, a model molecule with 1,9‐dihydroxyanthracene as the ESIPT parent core was designed and synthesized, which was proved to undergo twice cascaded ESIPT processes while the 1,8‐dihydroxynaphthalene‐based analogue can only undergo once ESIPT process based on DFT calculations and ultrafast dynamics analyses. Finally, a six‐level system lasing toward 900 nm was achieved with a low threshold of 27.4 μJ cm−2. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: Organic near‐infrared (NIR) luminescent materials have captured intense research interest owing to their potential applications in optical communication, data storage, bioimaging, sensing and night vision. Excited state intramolecular proton transfer (ESIPT) process with absorption in normal form while emission in tautomer form can lead to a distinct redshift emission, based on which, a lot of organic NIR luminescent materials were designed. Because of attractive features such as ultrahigh sensitivity to the surroundings, large Stokes shift, and inherent four level system, ESIPT based NIR luminescent materials are supposed to be ideal fluorescent probes and gain materials. In this review, first, organic near‐infrared luminescent materials based on ESIPT process are summarized according to the core structures. Second, recent advances of ESIPT‐based organic near‐infrared fluorescent probes and organic NIR lasers are reviewed. Finally, the current challenges and prospects of ESIPT‐based organic NIR luminescent materials are introduced. [ABSTRACT FROM AUTHOR]

The rapid development of information technology has resulted in a growing demand for low‐dimensional photonic materials. Organic semiconductor materials play an important role in various photonic devices due to their adjustable physicochemical properties, while individual organic crystals do not exhibit the desired performance due to the limitations of their simple structure. Branched organic crystals with inherent multichannel characteristics based on π‐conjugated molecules are favorable components in optoelectronics. However, the preparation of branched organic crystals still faces great challenges before they can be applied in integrated optoelectronic devices. In this Review, the development and representative examples of branched organic crystals in terms of molecular design, synthesis, and advanced applications are discussed. We also provide a summary and outlook for the direction of future research on branched organic crystals as excellent candidates in photonic integrated circuits. [ABSTRACT FROM AUTHOR]

The rapid development of information technology has resulted in a growing demand for low‐dimensional photonic materials. Organic semiconductor materials play an important role in various photonic devices due to their adjustable physicochemical properties, while individual organic crystals do not exhibit the desired performance due to the limitations of their simple structure. Branched organic crystals with inherent multichannel characteristics based on π‐conjugated molecules are favorable components in optoelectronics. However, the preparation of branched organic crystals still faces great challenges before they can be applied in integrated optoelectronic devices. In this Review, the development and representative examples of branched organic crystals in terms of molecular design, synthesis, and advanced applications are discussed. We also provide a summary and outlook for the direction of future research on branched organic crystals as excellent candidates in photonic integrated circuits. [ABSTRACT FROM AUTHOR]

In contrast to the widely reported excited-state single proton-transfer, excited-state multiple proton transfer (ESMPT) containing two or more intra- or inter-molecular proton transfers has greatly expanded the research scope of the excited-state proton transfers. In recent decades, ESMPT-active organic molecules have attracted much attention owing to their unique photophysical properties, such as large magnitude Stokes shifts and dual emission. These photophysical properties facilitate the application of the organic molecules in organic solid-state lasers, fluorescent probes and sensors, and molecular switches. Herein, we introduce the fundamentals of the ESMPT and review the recent advances in different types of ESMPTs in organic molecules. Finally, we present our conclusions and the future development prospects of the ESMPT in organic molecules. [ABSTRACT FROM AUTHOR]

Excited‐state intramolecular proton transfer (ESIPT)‐active organic semiconductor materials, characterized by a or several resonance‐assisted hydrogen bonds (RAHBs), are supposed to be ideal candidates for achieving high‐performance near‐infrared (NIR) lasers. However, according to the energy gap law, the development of ESIPT‐active gain materials is still limited by the serious nonradiative decays. Herein, it is demonstrated that RAHBs can activate ESIPT lasing by inhibiting nonradiative decays. A new ESIPT‐active material 1,5‐dihydroxy‐2,6‐diphenylanthraquinone (DP‐DHAQ) containing two centrosymmetric RAHBs is developed, which exhibits a ≈100‐fold higher radiative decay rate (kr = 1.1 × 1010 s–1) in doped polystyrene (PS) film than that of 1‐hydroxy‐5‐methoxy‐2,6‐diphenylanthraquinone (DP‐HMAQ) and 1,5‐dimethoxy‐2,6‐diphenylanthraquinone (DP‐DMAQ), in which one and two RAHBs are broken, respectively, by introducing methyl groups. Both DP‐DHAQ and DP‐HMAQ can form four‐level systems based on the ESIPT processes, but only DP‐DHAQ doped PS microspheres exhibit laser emission at 710 nm under the test conditions. It is worth mentioning that single‐crystal microplates of DP‐DHAQ can realize NIR laser emission at 725 nm. The results suggest that RAHBs can effectively activate the gain property of ESIPT‐active materials, which deepens insights into NIR ESIPT lasing and provides a new proposal for the design of organic laser‐active molecules. [ABSTRACT FROM AUTHOR]

Organic near‐infrared (NIR) emissive materials integrating the intrinsic NIR light advantages and organic semiconductor characters have generated immense scientific interest in fundamental science and practical application, including optical communications, night vision, surveillance, and biomedical applications. Nevertheless, the intrinsic energy gap law engenders a huge challenge to simultaneously meet longer emission wavelength and higher luminescence efficiency for organic NIR emitters. Herein, it is suggested that the purposefully molecular design and crystal engineering for novel organic NIR materials are urgently studied and explored. Herein, recent advances in novel organic NIR materials, mainly focusing on the hybridized local and charge transfer (HLCT) compounds, thermally activated delayed fluorescence (TADF) emitters, CT cocrystals, neutral π‐radicals, and excited‐state intramolecular proton transfer (ESIPT)‐active materials, are summarized. It is hoped that this perspective can afford a new insight into the fine design and synthesis of the desired organic NIR emitters. [ABSTRACT FROM AUTHOR]

In order to discover pesticidal lead compounds with high activity and low toxicity, a series of novel benzamides substituted with pyrazole-linked 1,2,4-oxadiazole were designed via bioisosterism. The chemical structures of the target compounds were confirmed via 1H NMR, 13C NMR and HRMS analysis. The preliminary bioassay showed that most compounds exhibited good lethal activities against Mythimna separate, Helicoverpa armigera, Ostrinia nubilalis and Spodoptera frugiperda at 500 mg/L. Particularly in the case of Mythimna separate, compound 14q (70%) exhibited obvious insecticidal activity. In addition, compound 14h demonstrated good fungicidal activity against Pyricularia oryae with an inhibition rate of 77.8%, and compounds 14e, 14k, 14n and 14r also showed certain antifungal activities (55.6–66.7%). The zebrafish toxicity test showed that the LC50 of compound 14h was 14.01 mg/L, which indicated that it may be used as a potential leading compound for further structural optimization. [ABSTRACT FROM AUTHOR]

Organic multiblock heterostructure nanowires (OMHNs), integrating distinct components in the same axial structure, have attracted much attention due to their excellent properties such as intrinsic good light confinement and rectification characteristics. However, rationally incorporating such features into OMHNs with rigorous 1D morphology control remains a key synthetic objective. It is because that the single components possess fundamentally distinctive properties such as size‐dependent electronic, optical, and magnetic features as well as lattice parameters. In the last decade, researchers made their own efforts to this exciting field, especially from the controlled fabrication to the advanced applications of the multiblock nanowires. As a result, various OMHNs have been developed as very promising candidates for high‐performance optoelectronic applications such as light harvesting, logic gate devices, photonic transistors, and photonic anticounterfeiting. Herein, the recent advances of OMHNs from the aspects of molecular design, synthesis, and advanced applications are reviewed, and an outlook is given providing inspiration for the future development of OMHNs toward integrated optoelectronic at nanoscale. [ABSTRACT FROM AUTHOR]

Thermally activated delayed fluorescent (TADF) materials have attracted increasing attention because of their ability to harvest triplet excitons via a reverse intersystem crossing process. TADF gain materials that can recycle triplet excitons for stimulated emission are considered for solving the triplet accumulation problem in electrically pumped organic solid‐state lasers (OSSLs). In this mini review, recent progress in TADF gain materials is summarized, and design principles are extracted from existing reports. The construction methods of resonators based on TADF gain materials are also introduced, and the challenges and perspectives for the future development of TADF gain materials are presented. It is hoped that this review will aid the advances in TADF gain materials and thus promote the development of electrically pumped OSSLs. [ABSTRACT FROM AUTHOR]

Organic heterostructure nanowires, such as multiblock, core/shell, branch-like and related compounds, have attracted chemists' extensive attention because of their novel physicochemical properties. However, owing to the difficulty in solving the lattice mismatch of distinct molecules, the construction of organic heterostructures at large scale remains challenging, which restricts its wide use in future applications. In this work, we define a concept of lattice-mismatch-free for hierarchical self-assembly of organic semiconductor molecules, allowing for the large-scale synthesis of organic heterostructure nanowires composed of the organic alloys and cocrystals. Thus, various types of organic triblock nanowires are prepared in large scale, and the length ratio of different segments of the triblock nanowires can be precisely regulated by changing the stoichiometric ratio of different components. These results pave the way towards fine synthesis of heterostructures in a large scale and facilitate their applications in organic optoelectronics at micro/nanoscale. The large-scale synthesis of organic heterostructure nanowires is challenging. Here, the authors report the synthesis of organic triblock nanowires via a lattice mismatch-free strategy. [ABSTRACT FROM AUTHOR]

Optical interconnects exhibit superior potential in the precise regulation of photon transmission for organic photonic circuits. However, the rational design of well‐defined organic heterostructures toward active optoelectronics remains challenging. Herein, we designed organic branched heterostructures (OBHs) with accurate spatial organization for optical interconnection. Notably, the precise regulation of OBHs has been controllably achieved including the trunk morphologies and the branched microwire number. Significantly, these as‐prepared OBHs inherently exhibit the multichannel coupling outputs and the excitation position‐dependent waveguide characteristics, leading to various outcoupling signals with tunable intensity and emission colors. The optical interconnects are realized due to the occurrence of exciton conversion and photon propagation between branch and trunk at the heterojunction, benefiting the application possibilities of two‐dimensional (2D) optical barcodes. [ABSTRACT FROM AUTHOR]

Optical interconnects exhibit superior potential in the precise regulation of photon transmission for organic photonic circuits. However, the rational design of well‐defined organic heterostructures toward active optoelectronics remains challenging. Herein, we designed organic branched heterostructures (OBHs) with accurate spatial organization for optical interconnection. Notably, the precise regulation of OBHs has been controllably achieved including the trunk morphologies and the branched microwire number. Significantly, these as‐prepared OBHs inherently exhibit the multichannel coupling outputs and the excitation position‐dependent waveguide characteristics, leading to various outcoupling signals with tunable intensity and emission colors. The optical interconnects are realized due to the occurrence of exciton conversion and photon propagation between branch and trunk at the heterojunction, benefiting the application possibilities of two‐dimensional (2D) optical barcodes. [ABSTRACT FROM AUTHOR]

Single‐crystalline micro‐/nanostructures based on organic stimulus‐responsive materials have attracted wide interests for their unique functional roles in various photonic applications including optical wave guiding, optical vapor sensing, and miniaturized lasing. Yet one imminent challenge is to pattern micro‐/nanostructured organic 1D arrays with controlled geometry, precise alignment, and pure crystallographic orientation owing to the uncontrollable dewetting dynamics in the solution processes. Herein, a smart assembly method is employed to regulate a confined crystallization of organic molecules. Sensitive, stable, and reproducible optical 1D‐array vapor sensors can detect the alkaline and acidic vapors based on the proton transfer process. As‐fabricated vapor sensors based on organic 1D arrays also selectively identify four similar amine vapors. Meanwhile, based on these 1D microstructure arrays, high‐performing Fabry–Pérot resonators with deep‐red laser emission, a low lasing threshold of 0.31 µJ, and high quality factor Q (≈2243) are realized. Owing to these multiple functions, organic microwire arrays not only provide intrinsic insight into optical vapor sensing but also offer guidance for the development of miniaturized lasers with specific functionalities, which show considerable potential in multifunctional photonic integrated circuits. [ABSTRACT FROM AUTHOR]

The controlled self-assembly of organic heterostructures (OHSs) with precisely defined compositions, architectures, and interfaces, have largely remained a challenge. Herein, we introduce an effective approach to accurately construct three types of axial branching OHSs including unilateral axial OHSs, bilateral single-branching axial OHSs and bilateral multi-branching axial OHSs through modulating hierarchical charge-transfer intermolecular interactions and sequential crystal nucleation rate on account of the two different cocrystals with the low lattice mismatching rate of ∼ 2.2%. The present work opens an avenue for rationally designing and finely synthesizing more kinds of OHSs. [ABSTRACT FROM AUTHOR]

Organic luminescent materials play an integral role in the optoelectronic applications of displays and solid-state lighting. Nevertheless, high-performance organic luminescent materials require the efficient combination of two or more kinds of materials, which is extremely difficult owing to the completely different self-assembly behaviors of multicomponent molecules. Herein, based on a broad scale from the molecular, micro-/nano-scale, and macroscopic levels, we successfully demonstrate the multiscale construction of organic luminescent microwires of cocrystals, solid solutions, and core-shell microstructures. Through the wide selection of electron donor/acceptor pairs, a series of color-tunable charge-transfer (CT) cocrystals are formed via the intermolecular cooperative self-assembly process. On this basis, the high structural compatibility and perfect lattice mismatching (∼1.1%) of cocrystals are critical factors that facilitate the combination of dissimilar materials to form solid solutions and core/shell microwires. Significantly, because of the full-spectrum light transport from 400 to 800 nm, the nano-micro-scaled solid solution microwires act as microscale white-light sources [CIE (0.32, 0.36)]. Meanwhile, the macroscopic-scale core/shell organic-microwires demonstrate tunable white-light emission with a high color-rendering index (CRI) of 83, whose CIE coordinates span from (0.37,0.39) to (0.40,0.31). Therefore, our work provides a feasible approach to the multiscale synthesis of novel luminescent organic semiconductor materials, which could lay a solid foundation for organic optoelectronics. [ABSTRACT FROM AUTHOR]