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INORGANICA CHIMICA ACTA · 2023 · IF 2.8

Synthesis, crystal structure and properties of Mn/Ni/Co 3D network structures based on 2, 5-bis(trifluoromethyl) terephthalic acid ligands

Ruiqin Huang,Wei Li,Xiaoling Luo,Zheng Liu,Guo-Cheng Han,Runzhi Wei

2,5-bis(trifluoromethyl)terephthalic acid (H 2 L 1 ) as the main ligand and 1,10′-phenanthroline (L 2 ) as the co-ligand were reacted with manganese chloride tetrahydrate (MnCl 2 ·4H 2 O), nickel sulfate hexahydrate (NiSO 4 ·6H 2 O) and cobalt nitrate hexahydrate (Co(NO 3 ) 2 ·6H 2 O) by solvothermal reaction to give the manganese complex [Mn 2 (L 1 ) 2 (L 2 ) 2 ] n ( 1 ), the nickel complex {[Ni 3 (L 1 ) 3 (L 2 ) 2 (H 2 O) 4 ]·2DMF} n ( 2 ) and the cobalt complex {[Co 2 (L 1 ) 2 (DMF) 2 ]·H 2 O} n ( 3 ). The structures were characterized and their properties studied by means of single-crystal X-ray diffraction, infrared spectroscopy, elemental analysis, ultraviolet spectroscopy, fluorescence spectroscopy, thermogravimetric analysis. The single-crystal structure analysis showed that the complexes 1 – 3 are infinitely extended three-dimensional network-like structures of space groups P 1 - , P 1 - , P 2 1 / n , respectively. The results of fluorescence analysis and thermogravimetric analysis showed that complexes 1 – 3 have good thermal stability and fluorescence properties, respectively. Complex 3 can also maintain good thermal stability at 230 °C, and the maximum fluorescence emission wavelength is 370 nm.

CAS / MDL: 7439-93-2
研究领域: 无机化学 · 材料科学
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CHEMISTRY-A EUROPEAN JOURNAL · 2019 ·Vol. 25 ·期 67 ·15401-15410 · IF 5.16

Polymorphous Luminescent Materials Based on ′T′-Shaped Molecules Bearing 4,7-Diphenylbenzo[c][1,2,5]thiadiazole Skeletons: Effect of Substituents on the Photophysical Properties

Gaowei Qian,Xiangbing Wang,Shengyue Wang,Yanqiong Zheng,Song Wang,Weiguo Zhu,Yafei Wang

Graphical Four ′T′-shaped molecules bearing the 2,1,3-benzothiadiazole skeleton were prepared and characterized. All compounds exhibited excellent thermal stability and polymorphism in the solid state. The structure–property relationship of these compounds was systematically explored. A highest external quantum efficiency of 6.15 %, beyond the theoretical value of fluorescence-based OLEDs (∼5 %), were achieved for the solution-processable OLEDs. Polymorphism, the intrinsic character of one chemical compound with at least two distinct phase arrangements, plays a very key role in the photophysical properties. In this contribution, four ′T′-shaped molecules bearing the 2,1,3-benzothiadiazole (BTD) skeleton, named 5 a – 5 d , were prepared and characterized. All compounds exhibited excellent thermal stability and polymorphism in the solid state, evident from thermogravimetric analysis, differential scanning calorimetry, and polarized optical microscopy results. Intense emissions with high photoluminescent quantum yields were achieved both in solution (56–97 %) and neat films (33–98 %). All compounds possessed clearly pH-dependent luminescence properties in solution. Additionally, compound 5 d showed useful mechanochromic luminescence owing to the transformation between the crystal and amorphous state. Employing compounds 5 a – 5 d as the dopant, solution-processable organic light-emitting diodes (OLEDs) were fabricated and presented a highest external quantum efficiency of 6.15 %, which is higher than the theoretical value of fluorescence-based OLEDs (∼5 %). This research provided a novel strategy for designing high-efficiency BTD-based polymorphic luminescent materials.

研究领域: 材料科学 · 光学 · 有机电子学
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Journal of Materials Chemistry A · 2015 ·Vol. 3 ·期 46 ·23149-23161 · IF 7.443

Synthesis and photovoltaic properties of two-dimensional benzodithiophene-thiophene copolymers with pendent rational naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole side chains

Xiaopeng Xu,Kui Feng,Kai Li,Qiang Peng

A series of new two-dimensional copolymers, PBDTT-TABT, PBDTT-TANT and PBDTT-TSNT, with conjugated benzodiathiazole (BT) or naphthobisthiadiazole (NT) side chains were successfully synthesized and characterized for high performance polymer solar cells (PSCs). The NT unit showed a stronger electron-withdrawing ability and a larger conjugation than the BT unit, which induced a stronger ICT process between the benzodithiophene (BDT)-thiophene (T) backbone and the conjugated side chain for NT containing copolymers. As a result, PBDTT-TANT and PBDTT-TSNT showed lower-lying bandgaps and more red-shifted absorption than PBDTT-TABT. The alkylthio modification effect of conjugated side chains was also investigated in this work. This effect showed a positive role in lowering the HOMO energy level, and a negative role in elevating carrier mobility and molecular stacking properties in our two-dimensional polymeric systems. Bulk heterojunction (BHJ) PSCs were fabricated using these copolymers as the donor materials to evaluate their photovoltaic properties. The PBDTT-TABT, PBDTT-TANT and PBDTT-TSNT devices exhibited PCEs of 4.60%, 5.65% and 4.01%, respectively. In spite of the Voc values, the highest Jsc, FF and PCE were achieved for the PBDTT-TANT device, which was attributed to its red-shifted absorption, improved carrier mobility and well-defined phase separation. It is interesting that the Jscs, FFs and PCEs of all these devices were elevated significantly when made using the solvent vapor annealing (SVA) method. The THF–SVA process would provide a driving force to facilitate the formation of a much more well-defined surface morphology, resulting in the enhanced Jsc and FF values. The PBDTT-TANT device showed the highest PCE of 8.04%, which is the top efficiency for this type of two-dimensional copolymer with donor (D)–donor (D) polymer backbones and donor (D)–acceptor (A) conjugated side chains. Our design strategy would give an instructive guide to developing high performance two-dimensional polymer donors to be used in organic photovoltaic applications.

研究领域: 材料科学 · 有机光电子学
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SYNTHETIC METALS · 2019 · IF 2.87

Electrochromic materials based on novel polymers containing triphenylamine units and benzo[c][1,2,5]thiadiazole units

Fanghong Ma,Fuhan Liu,Yanjun Hou,Haijun Niu,Cheng Wang

Six novel electrochromic (EC) polymers containing triphenylamine units and benzo[ c ][1,2,5]thiadiazole (BTD) units, coded as TPABTA, TPABTD, TPABTD-a, TPABTD-b, TPABTD-c and TPABTD-d, were successfully synthesized through polymer condensation reaction and their electrochromic properties were characterized in detail. The films of these polymers exhibited reversible color changes, high optical transparency, good solubility in many organic solvents and good coloration efficiency. Among them, the TPABTD-b film showed a set of reasonable electrochromic features, including high coloration efficiency (270 cm 2 ·C -1 ), appropriate transmittance change (23 % at 849 nm) and a relatively longer response time in bleaching process (t b  = 3.7 s).

研究领域: 材料科学 · 高分子化学
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DALTON TRANSACTIONS · 2014 ·Vol. 44 ·期 1 ·237-246 · IF 4.097

Multicolor (Vis-NIR) mesoporous silica nanospheres linked with lanthanide complexes using 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline for in vitro bioimaging

Ying Liu,Lining Sun,Jinliang Liu,Yu-Xin Peng,Xiaoqian Ge,Liyi Shi,Wei Huang

A novel mesoporous nanosphere functionalized with 3-(aminopropyl)triethoxysilane (APTES) and 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline (5-Br-Tip) was synthesized (denoted as Tip-MSS). With the coordinating function of the 5-Br-Tip to lanthanide (Ln) ions, for the first time, LnL3(5-Br-Tip) complexes were linked to the mesoporous nanospheres. The derived materials, named Ln-Tip-MSS (Ln = Eu, Tb, Sm, Nd, Yb), were characterized by Fourier-transform infrared (FT-IR) spectroscopy, TEM, XRD (wide-angle and small-angle), N2 adsorption/desorption analysis, and fluorescence spectroscopy. Upon excitation in the ligand absorption, the Ln-Tip-MSS nanomaterials show characteristic visible (Eu, Tb, Sm) and NIR (Sm, Nd, Yb) luminescence (multicolor emission covered from 450 nm to 1400 nm spectral region). Of importance is that, with low cytotoxicity and good biocompatibility given by the methyl thiazolyl tetrazolium (MTT) assay, the Eu-Tip-MSS was successfully applied to cell imaging in vitro based on the Eu3+ luminescence (under 405 nm excitation).

研究领域: 纳米医学 · 生物成像 · 材料科学 · 分子探针 · 化学生物学
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2020 · IF 2.888

Determination and correlation of ternary isobaric vapour-liquid equilibrium data of (dimethyl succinate + dimethyl glutarate + dimethyl adipate) at 2, 5 and 8 kPa

Chunli Zhi,Yang Tang,Jinru Wan,Xingming Liu,Honglin Chen,Xunqiu Wang

Isobaric vapour-liquid equilibrium data of {dimethyl succinate (DMS) + dimethyl glutarate (DMG) + dimethyl adipate (DMA)} ternary system was measured at 2 kPa, 5 kPa and 8 kPa with a dynamic recirculating apparatus and the temperature ranged from 364.46 to 403.55 K. The experimental data was correlated with NRTL, Wilson and Uniquac models. The results showed that the maximum value of the root mean square deviation of the vapour phase mole fraction of the ternary system correlated by the three models is 0.0083, 0.0076 and 0.0084, respectively. The vapour-liquid equilibrium data of the ternary system was predicted by the interaction parameters of NRTL, Wilson and the Uniquac models in the literature. The results showed that the maximum value of the root mean square deviation of the vapour phase mole fraction of the ternary system predicted by the three models is 0.0547, 0.0471, and 0.0498, respectively. The deviation between the experimental value and the regression value or the predicted value was small, and both met the needs of design calculation of the engineering separation. The results obtained from the regression of experimental values are significantly better.

研究领域: 化学工程 · 热力学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

One-step hydrothermal synthesis of CdxInyS(x+1.5y) for photocatalytic oxidation of biomass-derived 5-hydroxymethylfurfural to 2, 5-diformylfuran under ambient conditions

Ming Zhang,Zhihao Yu,Jian Xiong,Rui Zhang,Xinzhong Liu,Xuebin Lu

The Cd x In y S ( x +1.5 y ) catalysts with gradient Cd:In ratios were controllably synthesized via an one-step hydrothermal approach. Particularly, the hydrothermal synthesis conferred those Cd x In y S ( x +1.5 y ) catalysts with Cd:In ratios over 1:2 with a one-dimensional–three-dimensional heterojunction structure composed of CdS nanorods and cubic-phase CdIn 2 S 4 . Our characterization evidences reflected that the CdS nanorods effectively promoted the separation of photoexcited electron–hole pairs in Cd x In y S ( x +1.5 y ) and enabled transboundary transfer of photogenerated carriers. Spectroscopic and experimental results were further employed to develop a detailed catalytic mechanism, in which the superoxide anion (•O 2 − ) plays an important role in the catalytic oxidation of HMF to DFF by Cd x In y S ( x +1.5 y ) . Unlike other photocatalysts with •O 2 − as the main active species, Cd 1.5 In 2 S 4.5 gives an excellent performance in HMF conversion. This shows the great potential of cadmium–indium sulfides as photocatalysts for biomass conversion under ambient conditions.

研究领域: 材料科学 · 化学工程 · 环境科学 · 催化
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EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY · 2019 · IF 4.833

Design, synthesis and evaluation of novel diaryl-1,5-diazoles derivatives bearing morpholine as potent dual COX-2/5-LOX inhibitors and antitumor agents

Zhang Li,Zhong-Chang Wang,Xin Li,Muhammad Abbas,Song-Yu Wu,Shen-Zhen Ren,Qi-Xing Liu,Yi Liu,Peng-Wen Chen,Yong-Tao Duan,Peng-Cheng Lv,Hai-Liang Zhu

In this paper, 41 hybrid compounds containing diaryl-1,5-diazole and morpholine structures acting as dual COX-2/5-LOX inhibitors have been designed, synthesized and biologically evaluated. Most of them showed potent antiproliferative activities and COX-2/5-LOX inhibitory in vitro. Among them, compound A33 displayed the most potency against cancer cell lines (IC 50  = 6.43–10.97  μ M for F10, HeLa, A549 and MCF-7 cells), lower toxicity to non-cancer cells than celecoxib ( A33 : IC 50  = 194.01  μ M vs. celecoxib : IC 50  = 97.87  μ M for 293T cells), and excellent inhibitory activities on COX-2 (IC 50  = 0.17  μ M) and 5-LOX (IC 50  = 0.68  μ M). Meanwhile, the molecular modeling study was performed to position compound A33 into COX-2 and 5-LOX active sites to determine the probable binding models. Mechanistic studies demonstrated that compound A33 could block cell cycle in G2 phase and subsequently induced apoptosis of F10 cells. Furthermore, compound A33 could significantly inhibit tumor growth in F10-xenograft mouse model, and pharmacokinetic study of compound A33 indicated that it showed better stability in vivo . In general, compound A33 could be a promising candidate for cancer therapy.

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JOURNAL OF MATERIALS SCIENCE · 2021 ·Vol. 56 ·期 15 ·9344-9355 · IF 4.22

Electrospun Poly[poly(2,5-benzophenone)]bibenzopyrrolone/polyimide nanofiber membrane for high-temperature and strong-alkali supercapacitor

Fang Dan,Yan Bin,Agarwal Seema,Xu Wenhui,Zhang Qian,He Shuijian,Hou Haoqing

The separator is an important component for energy storage devices. At present, the membranes for supercapacitors are rare, especially the ones that work with an alkaline electrolyte. Herein, a type of flexible and highly porous polymer hybrid nanofiber membrane was prepared via a facile electrospinning process and served as a separator for supercapacitor’s work with strong alkaline electrolyte. As obtained, poly[poly(2,5-benzophenone)]bibenzopyrrolone/polyimide (PBPY/PI) membrane showed good thermal stability, high mechanical strength, large electrolyte uptake (452%), and fast ion conductivity (0.68 mS/cm). Moreover, PBPY/PI membrane exhibited excellent alkali resistance. The supercapacitor assembled with PBPY/PI membrane showed much better performance than those assembled with a commercial polypropylene membrane and electrospun polyimide nanofiber membrane and was found without capacitance loss after charge/discharge at 30 A/g for 10,000 cycles at 80 °C. The PBPY/PI membrane is a good candidate with temperature resistance and alkali resistance for high-performance supercapacitors.

CAS / MDL: 24937-79-9
研究领域: 材料科学 · 能源存储技术
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JOURNAL OF NUTRITIONAL BIOCHEMISTRY · 2020 · IF 4.873

Conjugated linoleic acid attenuates 2,4-dinitrofluorobenzene-induced atopic dermatitis in mice through dual inhibition of COX-2/5-LOX and TLR4/NF-κB signaling

Liu Tang,Xiao-Lei Li,Zi-Xin Deng,Yao Xiao,Ya-Hong Cheng,Jing Li,Hong Ding

Conjugated linoleic acid (CLA), commonly found in beef, lamb and dairy products, has been reported to exhibit anti-inflammatory and antipruritus effects and to inhibit the release of chemical mediators such as histamine and eicosanoid in laboratory rodents. The chief objective of the study is to assess the efficacy of CLA on atopic dermatitis (AD) in mice and to explore possible mechanisms with CLA treatments . To develop a new therapy for AD, the anti-AD potential of CLA was investigated by inducing AD-like skin lesions in mice using 2,4-dinitrofluorobenzene. We evaluated dermatitis severity; histopathological changes; serum levels of T helper (Th) cytokines (interferon-γ, interleukin-4); changes in protein expression by western blotting and immunohistochemistry staining for cyclooxygenase-2 (COX-2), 5-lipoxygenase (5-LOX), toll like receptor 4 (TLR-4), myeloid differentiation factor 88 (MyD88), nuclear factor-κB (NF-κB) and tumor necrosis factor α (TNF-α); and production of the proinflammatory lipid mediators, such as prostaglandin E 2 and leukotriene B4 , in the skin lesions. Treatment with CLA ameliorated the development of AD-like clinical symptoms and effectively inhibited epidermal hyperplasia and infiltration of mast cells and CD4 + T cells in the AD mouse skin. Total serum immunoglobulin E levels and the expression levels of Th1/Th2 cytokines and lipid mediators in dorsal skin were dramatically suppressed by CLA. Furthermore, CLA down-regulated the expressions of COX-2, 5-LOX, TLR4, MyD88, NF-κB and TNF-α. Taken together, our findings demonstrate the potential usefulness of CLA as an anti-inflammatory dietary supplement or drug for the prevention and management of AD skin diseases by modulating the COX-2/5-LOX and TLR4/MyD88/NF-κB signaling pathways .

研究领域: 免疫学 · 药理学 · 皮肤科 · 分子生物学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Oxygen-Vacancy-Engineered Cu/Cu2O/CuO@C nanocomposites from Copper–Furan 2, 5-Dicarboxylic acid Metal-Organic Framework: Unlocking catalytic Mastery in nitroarene hydrogenation

Haoheng Wu,Yanyan Yu,Ying He,Yun Liu

The development of high-performance, multifunctional catalysts capable of effectively addressing nitroarene hydrogenation remains a significant challenge. In this study, we present a novel approach to catalyst design through the controlled carbonization of a copper–furan dicarboxylate metal–organic framework (Cu-FDCA MOF), resulting in two distinct nanocomposites: oxygen-vacancy-rich Cu/Cu 2 O/CuO@C (synthesized in an argon atmosphere) and conventional CuO (prepared by air calcination). Advanced characterizations, including TEM, XPS, EPR, and BET, reveal that Cu/Cu 2 O/CuO@C possesses 2.3 times more oxygen vacancies and a surface area 97 times greater (106.21 m 2 /g vs. 1.09 m 2 /g) than CuO, which directly correlates with its superior catalytic performance. In the context of nitroarene hydrogenation, Cu/Cu 2 O/CuO@C demonstrates an exceptionally high rate constant (k app  = 25.33 × 10 -2 s -1 ), outperforming CuO by a factor of 40. Furthermore, Cu/Cu 2 O/CuO@C maintains 90 % of its catalytic activity after five reaction cycles and can be fully regenerated upon treatment at 400 °C. Through a combination of experimental studies and density functional theory (DFT) calculations, we propose a novel water-derived hydrogen transfer mechanism that challenges conventional understanding of the role of NaBH 4 . Notably, Cu/Cu 2 O/CuO@C also exhibits impressive versatility, efficiently degrading organic dye (Congo red/methylene blue/methyl blue) within three minutes. This work establishes MOF-derived oxygen-deficient nanocomposites as promising platforms for both amine synthesis and environmental decontamination.

CAS / MDL: 16940-66-2
研究领域: 材料科学 · 催化化学 · 环境科学
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RSC Advances · 2026 ·Vol. 16 ·期 15 ·13320-13331 · IF 6.1

Environmentally friendly fluorescence platform for detection of tetracycline in pharmaceutical formulations and human serums based on highly fluorescent 1,4-di-2-(5-phenyloxazolyl)-benzene

Muhammad S. Mustafa,Wrya O. Karim

Tetracycline (TC) is an efficient antibiotic used for curing different bacterial infections in both humans and animals. Accurate and precise detection of TC is a requisite for quality control of pharmaceutical productions and patient safety using a reliable method. This study presents a highly sensitive and selective strategy based on utilizing 1,4-di-2-(5-phenyloxazolyl)-benzene (POB) as a molecular fluorescence sensor for detecting TC. POB displays an optimal excitation and a high-intensity emission at 355 nm and 418 nm, respectively. The TC–POB interaction leads to a remarkable quenching of the fluorescence, allowing fluorometric detection of TC. A linear calibration curve in a range of 0.5–40 µM along with a limit of detection (LOD) of 0.143 µM was established. The analytical applicability of the developed method was estimated for measuring TC within pharmaceutical formulations and human serum samples, revealing high accuracy and precision. Ultimately, the greenness of the proposed method was inspected via the Analytical Greenness Metrics for Sample Preparation (AGREEprep) and the Analytical Greenness Index (BAGI), emphasizing the eco-friendly feature with respect to sample preparation steps, applicability, and practicability.

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