376 resultados para Viés
Resumo:
A new solvothermal route has been developed for synthesizing the size-controlled CdSe nanocrystals with relatively narrow size distribution, and the photoluminescence (PL) quantum yields (QYs) of the nanocrystals can reach 5-10%. Then the obtained CdSe nanocrystals served as cores to prepare the core/shell CdSe/CdS nanocrystals via a two-phase thermal approach, which exhibited much higher PL QYs (up to 18-40%) than the CdSe core nanocrystals. The nanocrystal samples were characterized by ultraviolet-visible (UV-vis) absorption spectra, PL spectra, wide-angle Xray diffraction (WAXD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM).
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Magnetic and conductive NiZn ferrite-polyaniline nanocomposites with novel core-shell structure have been fabricated by microemulsion process. The samples were characterized by XRD, TEM, SEM, IR, UV-vis, voltage/current detector and SQUID magnetometry. The core-shell structure of nanocomposites was observed by TEM. The changes of the magnetic and conductive properties after polyaniline coating were investigated.
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A novel solution-phase method for the preparation of Au@ZnO core-shell composites was described. With this method, the composites were grown without heating that is usually needed in other solution methods. Atomic force microscopy (AFM) results show that the diameter of Au@ZnO core-shell composites is about 10.5 nm. X-ray photoelectron spectroscopy (XPS) was applied to characterize Au@ZnO core-shell composites. The optical properties of Au@ZnO core-shell composites, including UV-vis absorption and photo luminescence (PL), were observed at room temperature.
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In this paper, a method for highly ordered assembly of cuprous oxide (Cu2O) nanoparticles (NPs) by DNA templates was reported. Cetyltrimethylammonium bromide (CTAB)-capped Cu2O NPs were adsorbed onto well-aligned lambda-DNA chains to form necklace-like one-dimensional (1D) nanostructures. UV-vis, atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) were used to characterize the nanostructure. The Cu2O nanostructures fabricated with the method are both highly ordered and quite straight.
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为了了解稀土元素与酶相互作用的化学机理,用紫外-可见(UV-Vis)吸收光谱技术和电化学方法研究了La3+与过氧化物酶(POD)的模型化合物,微过氧化物酶-8(MP-8)或微过氧化物酶-11(MP-11)的相互作用机理.La3+优先与MP-8或MP-11分子中血红素卟啉环上的2个丙酸基团的羰基氧发生键合作用,使它们的聚集程度降低,卟啉环的非平面性增加.由于MP-8分子聚集的倾向要小于MP-11,La3+使MP-8聚集程度的降低和卟啉环非平面性增加的程度要大于MP-11.由于MP-11的肽链较长而能形成螺旋状构象,使肽链上的羰基基团被包埋在肽链的疏水基团中,因此,La3+与MP-11中肽链上的羰基氧基本上不能发生键合作用.而MP-8的肽链较短,不能形成螺旋状结构,La3+也能与肽链上的羰基氧发生键合作用.
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用UV-Vis吸收光谱、荧光光谱、圆二色谱以及核磁共振光谱等手段研究了硫堇(TH)与两个不同序列寡核苷酸的作用。TH与寡核苷酸作用后的吸收光谱和荧光光谱产生了明显的减色红移和荧光猝灭效应。分别计算了TH与[oligo d(GC)]2和[oligo d(AT)]2作用的荧光猝灭常数和结合常数,结果表明TH与GC序列的结合能力比与AT序列更强。通过TH与[oligo d(GC)]2作用后双螺旋链构象变化以及TH质子的1HNMR谱峰明显变宽,进一步说明TH与寡核苷酸结合的序列选择性。
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Monolayer protected gold nanoparticles (MPCs) are the focus of recent research for their stability and are deemed as the building blocks of bottom-up strategies. In this Letter, 3-mercapto-1,2-propanediol monolayer protected gold nanoparticles (MPD-MPCs) were synthesized and characterized by transmission electron microscopy, UV/Vis spectroscopy, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The value of quantized double-layer capacitance (1.13 aF) of MPD-MPCs in aqueous media was obtained by differential pulse voltammograms.
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3-Mercaptopropionic add monolayer protected gold nanoclusters (MPA-MPCs) were synthesized and characterized by transmission electron microscopy, UV-Vis spectroscopy, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The exact value of quantized double-layer capacitance of MPCS in aqueous media was obtained by differential pulse voltammograms.
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In this paper, 4-ferrocene thiophenol was employed as a novel capping agent to synthesize electroactive gold nanoparticles. Transmission electron microscopy showed an average core diameter of 2.5 nm. The optical and electrochemical properties of the 4-ferrocene thiophenol capped gold nanoparticles were characterized by UV-Vis spectroscopy and cyclic voltammograms. Surface plasmon absorbance was detected at 522 nm. Cyclic voltammograms revealed the adsorbed layer reaction controlled electrode process, and the formal potential of electroactive ferrocene centers shifted anodically compared with ferrocene in solution, which could be attributed to the electron-withdrawing phenyl moiety linked to ferrocene.
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In this article, we employed triphenylmethanethiol (TPMT) as a novel rigid agent for capping gold nanoparticles and the TPMT monolayer-protected gold nanoparticles were characterized by various analytical techniques. High-resolution transmission electron microscopy showed a narrow dispersed gold core with an average core diameter of ca. 3.6 nm. The UV/vis spectrum revealed the surface plasmon absorbance at 528 nm. The p-pi conjugated structure of the TPMT ligand was confirmed by nuclear magnetic resonance. Differential scanning calorimetry and Fourier transform infrared spectroscopy revealed the rigid nature of the TPMT chains.
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Numerous reports have focused on ferrocene-terminated electroactive self-assembled monolayers (SAMs) on a flat An surface but only a few on ferrocene SAMs on An colloid. In this paper, we employ 4-ferrocene thiophenol as a novel capping agent to produce electroactive gold nanoparticles in consideration of the peculiar pi-conjugated structure. Transmission electron microscopy shows the narrow-dispersed gold core with an average core diameter of ca. 2.5 nm. UV/vis spectra examine the pi-conjugated structure of 4-ferrocene thiophenol and surface plasmon absorbance of the indicated gold nanoparticles. X-ray photoelectron spectroscopy reveals electronic properties of the An core and thiol ligands. Electrochemical measurement shows that the oxidation peak current is proportional to the scan rate, indicating the electrode process is controlled by adsorbed layer reaction. The formal potential of the Fc-MPCs is compared with that of free ferrocene in MeCN solution and the Fc-SAMs. The shifts are attributed to the phenyl moiety in the 4-ferrocene thiophenol and dielectric constant of the solvation environment.
Resumo:
Two new light-emitting PPV-based copolymers bearing electron-withdrawing triazole unit in the main chain have been synthesized by Wittig reaction between triazole diphosphonium salt and the corresponding dialdehyde monomers, respectively. Their optical and physical properties are characterized by UV-vis, photoluminescence (PL), TGA and DSC. The resulting copolymers are highly soluble in common organic solvents and have high Tg and Td values. They show blue-greenish fluorescence in solution (lambda(max) 502 and 508 nm) and green fluorescence in the solid state (lambda(max) 520 and 526 nm), respectively.
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Two PPV-based copolymers consisting siloxane linkage have been synthesized by melt condensation of bisphenol and dianilinodimethylsilane. The rigid PPV segments act as chromosphere and allow fine turning of band gap for blue-light emission, while the flexible siloxane units lead to the effective interruption of conjugation and the enhancement of solubility. The UV-vis absorption, photoluminescent and eletroluminescent properties have been studied.
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A PPV derivative containing bulky tetraphenylmethane side chains was synthesised. Its optical properties were examined. Compared to its parent PPV polymer, its UV-Vis absorption and PL showed less red-shift from solution to film, its PL showed much less concentration quenching effect and higher efficiency, its EL device showed 9-fold enhanced efficiency. These improvements were attributed to weakened inter-chain interaction caused by the tetraphenylmethane group.
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Perovskite-type organic/inorganic hybrid layered compound (C6H5C2H4NH3)(2)PbI4 was synthesized. The patterning Of (C6H5C2H4NH3)(2)PbI4 thin films on silicon substrate was realized by the micromolding in capillaries (MIMIC) process, a kind of soft lithography. Bright green luminescent stripes with different widths (50, 15, 0.8 mum) have been obtained. The structure and optical properties Of (C6H5C2H4NH3)(2)PbI4 films were characterized by X-ray diffraction (XRD), UV/Vis absorption and photoluminescence excitation and emission spectra, respectively. It is shown that the organic-inorganic layered (C6H5C2H4NH3)(2)PbI4 film was c-axis oriented, paralleling to the substrate plane. Green exciton emission at 525 nm was observed in the film, and the explanations for it were given.