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141.
Xiaolong Shi Xiaoru Zhao Libing Duan Huinan Sun Jinming Liu Xiaojun Bai Mengmeng Guan Mengmeng Cao Jinru Liu 《Journal of Sol-Gel Science and Technology》2013,66(2):301-305
Sn-doped ZnO (SZO) thin films are deposited by sol–gel dip-coating method with Sn content at 0 at.% and 1–15 at.% with an increment of 2 at.%. The structure and luminescence of the films are investigated. X-ray diffraction results indicate that all the SZO samples show preferential orientation along the (002) direction, and the scanning electron microscope exhibits that the surface morphology of the films change from nanoparticles to nanorods with increasing Sn concentration. X-ray photoelectron spectroscopy reveals that Sn exists as valence of +4 in the matrix. The photoluminescence peaks at 381 and 398 nm are observed in all the samples. The ratio of intensity of peak at 381 nm to that of peak at 398 nm differed markedly. The intensity of peak at 398 nm might be due to the response for the Sn atoms, while the intensity of peak at 381 nm is probably related to the quantum size effect. 相似文献
142.
The polyhydroxyurethane/attapulgite nanocomposites (PHU/ATP) were prepared by in-situ surface-initiated polymerization of a five-membered cyclic carbonate, 2, 2-bis [p-(1, 3-dioxolan-2-one-4-yl-methoxy) phenyl] propane (B5CC) and hexamethylene diamine, from the surface of the aminopropyl attapulgite nanoparticles (APATP) for the first time. The chemical grafting of the polymer on the surface of ATP was confirmed by FTIR and the morphology of the attapulgite nanoparticles in the nanocomposites was examined by TEM. The thermal stabilities of the polyhydroxyurethane (PHU) and the polyhydroxyurethane/attapulgite nanocomposites (PHU/ATP) were compared with thermogravimetric analysis (TGA).The %G of the attapulgite nanoparticles was also calculated from the results of TGA after the free polyhydroxyurethane was washed off. 相似文献
143.
Temperature-depended handedness inversion in chiral mesoporous silica was investigated by diffuse-reflectance circular dichroism spectra. 相似文献
144.
许多疾病的特征在于各种生物分子表现出的异常活性,这些物质通常在细胞内外显示过表达现象,因此对其灵敏靶向识别可以提供诊断和治疗效用。由于基因诊疗和化学传感技术的发展,用于灵敏检测细胞内外生物化学物质的核酸探针突显优势。核酸探针可以在稳定进入细胞的同时,特异性地结合目标物质,通过光学方法检测或通过成像技术标识出来。本文综述了采用光学传感方法和成像技术,基于核酸探针检测生物分子的新进展。根据检测对象进行分类,概括分析了几个代表性体系:核酸序列、蛋白质和酶、化学物质和物理化学条件,并详细阐述其关键设计原理、灵敏度及样品检测等结果,同时指出了各类核酸探针的优缺点。 相似文献
145.
Promoting electron mobility is the key to designing high performance electron transport materials(ETMs). Formation of intermolecular interaction can be helpful to enhance their electron mobilities as a result of more ordered molecular stacking.Here, to reveal the inherent influence of intermolecular π-π stacking on the electron mobilities, we designed two ETMs, namely,2,4-diphenyl-6-[3-(2-triphenylenyl)phenyl]-1,3,5-triazine(TPTRZ) and 2,4-diphenyl-6-[4′-(2-triphenylenyl)[1,1′-biphenyl]-3-yl]-1,3,5-triazine(TPPTRZ). Thermal, photophysical and electrochemical measurement results indicate they are good ETM candidates. Additionally, TPTRZ and TPPTRZ exhibit high electron mobilities of 3.60×10~(-5) and 3.58×10~(-5) cm~2V-1 s~(-1), respectively, at an electric field of 7×10~5 V cm~(-1). By taking X-ray single crystal structure, theoretical calculation and time of flight(TOF) results into consideration, it is revealed that strong intermolecular π-π stacking induced by planar triphenylene and triphenyltriazine units renders TPTRZ and TPPTRZ small energetic and positional disorder parameters, and results in their high electron mobilities thereby. By further enhancing intermolecular π-π stacking, ETMs with even higher electron mobilities can thus be anticipated. 相似文献
146.
The effect of the impregnation and co-precipitation-kneading methods on the catalytic performance of the Ni/H-ZSM-5 catalyst was evaluated via catalytic reductive deoxygenation of cyclohexanone in a fixed bed. The catalysts were characterized by X-ray diffraction, nitrogen adsorption, and NH3-temperature programmed desorption. A sharply acidic and textural change was observed on the catalysts prepared by the different methods, while the metal active phase structure was almost the same. The results of the cyclohexanone reductive deoxygenation reaction indicated that the catalyst based on the co-precipitation-kneading method afforded a higher yield of cyclohexane, and thus proved that the co-precipitation-kneading method is suitable for the preparation of a bi-functional catalyst. 相似文献
147.
148.
Guo‐Ying Hong Zhong‐Xin Zhu Yuan‐Meng Duan Xuan Zhou Li‐Tai Jin 《Electrophoresis》2013,34(22-23):3171-3179
As a noncovalent fluorescence probe, in this study, salicylaldehyde azine (SA) was introduced as a sensitive fluorescence‐based dye for detecting proteins both in 1D and 2D polyacrylamide electrophoresis gels. Down to 0.2 ng of single protein band could be detected within 1 h, which is similar to that of glutaraldehyde‐silver stain, but approximately four times higher than that of SYPRO Ruby fluorescent stain. Furthermore, comparative analysis of the MS compatibility of SA stain with SYPRO Ruby stain indicated that SA stain is compatible with the downstream of protein identification by LC‐MS/MS. Additionally, the probable mechanism of the SA stain was investigated by molecular docking. The results demonstrated that the interaction between SA and protein was mainly contributed by hydrogen bonding and hydrophobic forces. 相似文献
149.
Triazolo‐fused 2′,3′‐cyclic nucleoside analogs were synthesized by an intramolecular 1,3‐dipolar cycloaddition of nucleoside‐derived azido alkynes in a regio‐ and stereospecific manner. The uracil base in these target compounds was successfully transformed to the corresponding cytosine. The synthesized compounds were examined in a MAGI assay for their anti‐HIV activities, and in a H9 T lymphocytes assay for their cell toxicities. 相似文献
150.
Inspired by the idea of charge decomposition in calculation of the dipole preserving and polarization consistent charges (Zhang et al., J. Comput. Chem. 2011, 32, 2127), we have proposed a numerically stable restrained electrostatic potential (ESP)‐based charge fitting method for protein. The atomic charge is composed of two parts. The dominant part is fixed to a predefined value (e.g., AMBER charge), and the residual part is to be determined by restrained fitting to residual ESP on grid points around the molecule. Nonuniform weighting factors as a function of the dominant charge are assigned to the atoms. Because the residual part is several folds to several orders smaller than the dominant part, the impact of ill‐conditioning is alleviated. This charge fitting method can be used in quantum mechanical/molecular mechanical (QM/MM) simulations and similar studies, where QM calculated electronic properties are frequently mapped to partial atomic charges. © 2012 Wiley Periodicals, Inc. 相似文献