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111.
Christian J. Mueller Chetan R. Singh Mukundan Thelakkat 《Journal of Polymer Science.Polymer Physics》2016,54(6):639-648
To obtain novel low‐bandgap materials with tailored hole‐transport properties and extended absorption, electron rich 3,4‐ethylenedioxythiophene is introduced as a comonomer in diketopyrrolo[3,4‐c]pyrrole copolymers with different aryl flanking units. The polymers are characterized by absorption and photoluminescence spectroscopy, dynamic scanning calorimetry, cyclic voltammetry, and X‐ray diffraction. The charge transport properties of these new materials are studied carefully using an organic field effect transistor geometry where the charge carriers are transported over a narrow channel at the semiconductor/dielectric interface. These results are compared to bulk charge carrier mobilities using space‐charge limited current (SCLC) measurements, in which the charge carrier is transported through the complete film thickness of several hundred nanometers. Finally, charge carrier mobilities are correlated with the electronic structure of the compounds. We find that in particular the thiophene‐flanked copolymer PDPP[T]2‐EDOT is a very promising candidate for organic photovoltaics, showing an absorption response in the near infrared region with an optical bandgap of 1.15 eV and a very high bulk hole mobility of 2.9 × 10?4 cm2 V?1 s?1 as measured by SCLC. This value is two orders of magnitudes higher than SCLC mobilities reported for other polydiketopyrrolopyrroles and is in the range of the well‐known hole transporting polymer poly(3‐hexylthiophene). © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 639–648 相似文献
112.
Bioassay‐guided isolation of an active compound with protein tyrosine phosphatase 1B inhibitory activity from Sargassum fusiforme by high‐speed counter‐current chromatography 下载免费PDF全文
Miao Wang Xinfeng Guo Haoquan Li Yi Wang Hong Guo Yi Yang Jing Tian 《Journal of separation science》2016,39(22):4408-4414
A rapid and efficient method using high‐speed counter‐current chromatography was established for the bioassay‐guided separation of an active compound with protein tyrosine phosphatase 1B inhibitory activity from Sargassum fusiforme. Under the bioassay guidance, the ethyl acetate extract with the best IC50 value of 0.37 ± 0.07 μg/mL exhibited a potential protein tyrosine phosphatase 1B inhibitory activity, which was further separated by high‐speed counter‐current chromatography. The separation was performed with a two‐phase solvent system composed of n‐hexane/methanol/water (5:4:1, v/v). As a result, dibutyl phthalate (19.7 mg) with the purity of 95.3% was obtained from 200 mg of the ethyl acetate extract. Its IC50 was 14.05 ± 0.06 μM, which was further explained by molecular docking. The result of molecular docking showed that dibutyl phthalate enfolded in the catalytic site of protein tyrosine phosphatase 1B. The main force between dibutyl phthalate and protein tyrosine phosphatase 1B was the hydrogen bond interaction with Gln266. In addition, hydrogen bond, van der Waals force and hydrophobic interaction with the amino acids (Ala217, Ile219, and Gly220) were also responsible for the stable protein‐ligand complex. 相似文献
113.
F. Namouchi H. Guermazi C. Zerrouki S. Agnel J.J. Bonnet 《European Polymer Journal》2007,43(11):4821-4829
Charges evolution in poly(methyl methacrylate) (PMMA) samples under thermal aging effect has been studied by means of two complementary techniques, thermal step method (TSM) and thermally stimulated depolarization current (TSDC). For the first method, measurements reveal that injected charges, whose quantity is found depending on the number of applied temperature cycles, remain close to the surface sample. TSDC measurements have been carried out for different temperatures ranging from 25 °C to 140 °C. Three distinguishable dipolar relaxations (β1, β2 and α) have been highlighted. In the same way, the presence of polarization and injected charges has been confirmed. In support of electric characterization, X-ray reflectometry has been used. The obtained results equally emphasized the thermal aging effect on the material. 相似文献
114.
Effects of Neutron Irradiation on Superconducting Properties of GdBa2Cu3O7-δ Single Domain Superconductor 下载免费PDF全文
The effects of neutron irradiation with a fluence of 1015 n/cm2 on the superconducting properties of GdBa2Cu3O7-δsingle domain sample were studied. The point and cascade defects produced by the neutron irradiation were observed by high-resolution transmission electron microscopy. The cascade defects were found to have the sizes of about 4-7 nm which is comparable to the coherence lengths of high temperature superconductors. The point defects disappear while the cascades still exist through thermal annealing. The temperature dependence of magnetization for the magnetic field parallel to the crystallographic c axis shows that the neutron irradiation leads to a dramatic degradation of uperconductivity for the as-irradiated sample, a decrease of critical current density (Jc), and the weakening of the fishtail effect in the Jc versus magnetic induction B curve. However, for the as-irradiated sample annealed in the flowing oxygen atmosphere, it shows that Jc under high magnetic fields is greatly enhanced, the fishtail shifts towards higher magnetic fields, and its superconductivity is partially recovered as well due to the remaining effecive pinning centers of the cascades. These results suggest a prospective application for such a treated GdBa2Cu3O7-δsuperconductor. 相似文献
115.
国内现有化学微课的整体水平可以从3个角度进行分析: 拍摄方式、拍摄内容和拍摄技术。分析精品化学微课, 主要有4个典型特征。关于微课使用, 提出了精品微课在“翻转课堂”中需要“自主任务学习单”支撑的观点。对于未来的微课创作与使用, 需要破除6大疑惑, 解决创作中的8大问题。 相似文献
116.
Ru-Ir-Ti氧化物阳极正反电流电解失效机理研究 总被引:2,自引:0,他引:2
应用热分解法制备适用于海水电解的钛基金属氧化物阳极.由SEM、EDX和XRD分析表征该阳极的形貌、成分及相结构,结果表明,烧结后阳极表面形成了固溶体结构,分别为(Ru,Ir,Ti)O2和(Ir,Ti)O2,失效后氧化物阳极的固溶体结构几乎完全消失,活性物质丧失.强化正反向电流寿命测试、循环伏安曲线和电化学阻抗谱等测试表明,失效后氧化物阳极表面的电化学活性点大大减少,同时膜电阻增加,这是由于活性物质脱落导致的,进一步说明正反向电流导致阳极表面活性物质脱落是氧化物阳极失效的根本原因. 相似文献
117.
118.
The aromaticity of metal-metal quintuple bonded complexes of the type M2L2 (M=Cr, Mo, and W; L=amidinate) are studied employing gauge including magnetically induced ring current (GIMIC) analysis and electron density of delocalized bonds (EDDB). It is found that the complexes possess two types of aromaticity: i) Hückel aromaticity through delocalization of ligand π electrons with metal-metal δ-bond-forming 6 conjugated electrons (4π and 2δ) ring; ii) Craig-Möbius aromaticity through delocalization of π electrons of both the ligands with metal d-orbitals in Craig type orientation forming 10π electrons ring with a double twist. Extended transition state natural orbital chemical valence (ETS-NOCV) and canonical molecular orbital natural chemical shielding (CMO-NCS) analysis confirm the Craig-Möbius type arrangement of the orbitals. Furthermore, the unprecedented Hückel and Möbius type aromaticity is confirmed from the plot of the current pathways using 3D line integral convolution (3D-LIC) plots. The metal-metal bond order also increases down the group as justified from the complete active space self-consistent field (CASSCF) analysis. Due to an increase in the π and δ electron conjugation, both the Hückel and Möbius aromaticity increase down the group. 相似文献
119.
Milivoj Lovrić 《Electroanalysis》2021,33(11):2372-2380
A model of cyclic staircase voltammetry of enzymatic reactions on the rotating disk electrode is developed and the inhibition by the product is investigated. The responses are mostly time – dependent current – potential curves with maxima in the forward but not in the backward branch. If the maxima appear in both branches, the inhibition is potential – dependent either directly or indirectly. The source of the second maximum is explained. 相似文献
120.
《Journal of computational chemistry》2017,38(3):144-151
An increasing number of observations show that non‐classical isomers may play an important role in the formation of fullerenes and their exo‐ and endo‐derivatives. A quantum‐mechanical study of all classical isomers of C58, C60, and C62, and all non‐classical isomers with at most one square or heptagonal face, was carried out. Calculations at the B3LYP/6‐31G* level show that the favored isomers of C58, C60, and C62 have closely related structures and suggest plausible inter‐conversion and growth pathways among low‐energy isomers. Similarity of the favored structures is reinforced by comparison of calculated ring currents induced on faces of these polyhedral cages by radial external magnetic fields, implying patterns of magnetic response similar to those of the stable, isolated‐pentagon C60 molecule. © 2016 Wiley Periodicals, Inc. 相似文献