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RSC Advances · 2017 ·Vol. 7 ·期 82 ·52024-52029 · IF 3.108

Modulating molecular structures and dielectric transitions in organic–inorganic hybrid crystals

Xiao-Fen Sun,Zhongxia Wang,Wei-Qiang Liao,Peng-Fei Li,Jixing Gao,Yi-Yang Huang,Hai-Peng Chen,Heng-Yun Ye,Yi Zhang

In this paper, three new hybrid phase transition compounds, [Hmpy]CdBr3 (1, Hmpy = N-methylpyrrolidinuium cation), [Hmpy]2CdBr4 (2) and [Hmpy]3CdBr3·CdBr4 (3), were synthetized by means of regulating the ratio of reactants. Systematic characterizations consisting of variable temperature X-ray single crystal diffraction, differential scanning calorimetry (DSC) and dielectric measurements reveal that 1 with infinite one-dimensional (1D) [CdBr3]n− chains undergoes a phase transition around 278 K; 2 with isolated [CdBr4]2− tetrahedrons exhibits a high-temperature phase transition close to 367 K, accompanied by prominent switchable dielectric behavior. Interestingly, 1D [CdBr3]n− chains and isolated [CdBr4]2− tetrahedrons both exist in 3, associated with a phase transition at 320 K. The phase transitions in the three compounds are originated from the order-disorder transitions of the Hmpy cation. It is expected that our finding would promote the development of hybrid dielectric transition materials with adjustable properties.

研究领域: 材料化学 · 凝聚态物理 · 晶体工程 · 功能材料 · 介电材料
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Interfacial architecting of organic–inorganic hybrid toward mechanically reinforced, fire-resistant and smoke-suppressed polyurethane composites

Pingfan Xu,Yaofa Luo,Peikun Zhang

Polyurethane (PU) composites integrated with outstanding fire retardancy, smoke suppression as well as ameliorated mechanical property is attractive, but remains a challenge. Here, we demonstrate the interfacial architecting of organic–inorganic hybrid (ACAPP) by reacting renewable chitooligosaccharide (COS) with ammonium polyphosphate (APP) and ammonium octamolybdate (AOM) via a one-pot, facile and eco-friendly approach. The ACAPP with multiple hydroxyl groups shows good compatibility and strong interfacial adhesion force with PU matrix due to the abundant covalent cross-linking points and hydrogen bonds networks. The incorporation of 15 wt% ACAPP enables the resultant PU composite to achieve a V-0 rating, a limiting oxygen index of 26.1%, 31.1% and 44.8% reduction in total heat release and total smoke production, respectively, far outdistancing conventional APP. The suppressed fire hazards mainly benefits from the synergy catalytic carbonization effect of ACAPP in condensed phase. Moreover, ACAPP reinforces the tensile strength of PU whilst retaining the decent ultimate elongation. This work may offer a referable exemplification for constructing green flame-retardant to balance high fire safety and mechanical properties.

研究领域: 高分子材料科学 · 阻燃化学 · 复合材料工程 · 绿色化学 · 材料界面科学
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POLYHEDRON · 2016 · IF 2.108

Growth, structure, optical and thermal properties of three new organic–inorganic hybrid crystals: (C2H7N4S)3BiCl6·H2O, (C2H7N4S)2BiBr5, and (C2H5N4S)2BiI5

Tongguang Sun,Fei Liang,Xinyuan Zhang,Heng Tu,Zheshuai Lin,Guochun Zhang,Yicheng Wu

Single crystals of three new organic–inorganic hybrid compounds, tri[1-(diaminomethylene)uronium] hexachlorobismuthate ((C 2 H 7 N 4 S) 3 BiCl 6 ·H 2 O, HATU-BCH), bis[1-(diaminomethylene)uronium] pentabromobismuthate, ((C 2 H 7 N 4 S) 2 BiBr 5 , HATU-BB), and bis [3,5-diamino-1,2,4-thiadiazol-2-ium] pentaiodobismuthate ((C 2 H 5 N 4 S) 2 BiI 5 , OHATU-BI), have been successfully grown by slow evaporation method. Their structures were determined by single - crystal X-ray diffraction, in which all anion sublattice structures consist of hexahalobismuthates octahedra with different connection modes involving isolated, shared-corner, and shared-edge. The spectra characters were studied by Infrared and Raman spectra, which interpreted by calculation of the density functional theory (DFT) method and diffuse reflectance spectra. Thermal properties were characterized by thermal gravimetric analysis and differential scanning calorimetry.

研究领域: 材料化学 · 晶体工程 · 配位化学 · 光谱学 · 热分析 · 计算化学
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NEW JOURNAL OF CHEMISTRY · 2020 ·Vol. 44 ·期 33 ·14103-14107 · IF 3.288

Synthesis, structure and photoluminescence properties of three copper(I) iodide based inorganic–organic hybrid structures with pyrazine derivatives

Chanchan Xu,Le Lv,Dawei Luo,Wei Liu

By using pyrazine derivatives, three different types of copper(I) iodide based inorganic–organic hybrid structures, 1D-CuI(2-mo-pz) (1, 2-mo-pz = 2-methoxy-pyrazine), 2D-CuI(2,3-dm-pz)0.5 (2, 2,3-dm-pz = 2,3-dimethyl-pyrazine), and 2D-Cu2I2(2,5-dm-pz)2 (3, 2,5-dm-pz = 2,5-dimethyl-pyrazine), have been obtained by using a slow-diffusion method. Single crystal and powder X-ray diffraction analyses reveal that these hybrid structures are a one-dimensional (1D) staircase chain based structure, two-dimensional (2D) staircase-chain based structure, and 2D rhomboid dimer based structure, respectively. All of the three compounds show photoluminescence, with the internal quantum yield (IQY) as high as 88.2% for 1. This work provides evidence that for this type of hybrid materials, the structure of the inorganic module could be determined by the selection of the organic ligands and that the substituted group on the organic ligands can influence the luminescence efficiency of the hybrid structures.

研究领域: 无机化学 · 材料化学 · 配位化学 · 光物理 · 功能材料
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Advanced Optical Materials · 2022 ·Vol. 10 ·期 15 ·2200605 · IF 10.05

Highly Reversible Moisture-Induced Bright Self-Trapped Exciton Emissions in a Copper-Based Organic–Inorganic Hybrid Metal Halide

Shaofan Fang,Bo Zhou,Huixia Li,Hanlin Hu,Haizhe Zhong,Henan Li,Yumeng Shi

Metal halide perovskites are promising optoelectronic materials due to their unique luminescent properties. However, their practical application is limited by their poor chemical stability, especially in humid environments. Moisture can cause phase changes or chemical decomposition, resulting in significant fluorescence quenching. In this study, a copper-based organic–inorganic hybrid metal halide (t-BA) 3 Cu 6 I 9 is synthesized (t-BA + is the tert-butyl-ammonium ion (C(CH 3 ) 3 NH 3 + )). This material exhibits water-induced luminescence, and its chemical stability in humid environments is being investigated. Tetragonal t-BA 3 Cu 6 I 9 is not luminescent, but it reacts quickly with water in the air. The resultant (t-BA) 2 Cu 2 I 4 ·H 2 O has a broad green emission peak at 520 nm, high photoluminescence quantum yield of 59.4%. Remarkably, (t-BA) 2 Cu 2 I 4 ·H 2 O is converted back to t-BA 3 Cu 6 I 9 at temperatures above 40 °C. This phase conversion is highly repeatable, and the luminescent intensity can be fully recovered after 50 transformation cycles. The mechanism of luminescence is investigated through temperature-dependent photoluminescence spectra and theoretical calculation, which suggests that (t-BA) 2 Cu 2 I 4 ·H 2 O has a more localized charge distribution and sufficient polyhedral distortion, resulting in a bright and efficient emission from self-trapped excitons. This is the first report of water-induced luminescence in copper-based metal halides, and it paves the way for stable luminescent materials that are responsive to humidity.

研究领域: 材料化学 · 光物理学 · 无机化学 · 功能材料 · 发光材料
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JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES · 2014 · IF 2.694

Novel regenerative large-volume immobilized enzyme reactor: Preparation, characterization and application

Guihua Ruan,Meiping Wei,Zhengyi Chen,Rihui Su,Fuyou Du,Yanjie Zheng

A novel large-volume immobilized enzyme reactor (IMER) on small column was prepared with organic–inorganic hybrid silica particles and applied for fast (10   min) and oriented digestion of protein. At first, a thin enzyme support layer was formed in the bottom of the small column by polymerization with α-methacrylic acid and dimethacrylate. After that, amino SiO 2 particles was prepared by the sol–gel method with tetraethoxysilane and 3-aminopropyltriethoxysilane. Subsequently, the amino SiO 2 particles were activated by glutaraldehyde for covalent immobilization of trypsin. Digestive capability of large-volume IMER for proteins was investigated by using bovine serum albumin (BSA), cytochrome c (Cyt- c ) as model proteins. Results showed that although the sequence coverage of the BSA (20%) and Cyt- c (19%) was low, the large-volume IMER could produce peptides with stable specific sequence at 101–105, 156–160, 205–209, 212–218, 229–232, 257–263 and 473–451 of the amino sequence of BSA when digesting 1   mg/mL BSA. Eight of common peptides were observed during each of the ten runs of large-volume IMER. Besides, the IMER could be easily regenerated by reactivating with GA and cross-linking with trypsin after breaking the –C N– bond by 0.01   M HCl. The sequence coverage of BSA from regenerated IMER increased to 25% comparing the non-regenerated IMER (17%). 14 common peptides. accounting for 87.5% of first use of IMER, were produced both with IMER and regenerated IMER. When the IMER was applied for ginkgo albumin digestion, the sequence coverage of two main proteins of ginkgo, ginnacin and legumin, was 56% and 55%, respectively. (Reviewer 2) Above all, the fast and selective digestion property of the large-volume IMER indicated that the regenerative IMER could be tentatively used for the production of potential bioactive peptides and the study of oriented protein digestion.

研究领域: 生物化学 · 分子生物学 · 蛋白质组学 · 酶工程 · 生物材料
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