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951.
Xianghua Zeng Zhimei Li Zhiyin Xiao Yanwei Wang Xiaoming Liu 《Electrochemistry communications》2010,12(3):342-345
The synthesis and characterisation of two diiron hexacarbonyl complexes [Fe2(SXS)(CO)6], 1 (SXS = ((?SCH2)2C(CH3)CH2OCOFc, Fc = ferrocenyl group) and 2 (SXS = (?SCH2CH2NHCOFc)2), were described. By using intramolecularly integrated ferrocenyl group(s) in the complexes as an internal standard, the nature of two stepwise one-electron processes of the complexes coupled with a chemical reaction was clearly demonstrated. Examining how the reduction transformed into sole one-electron process with both increasing scanning rate under Ar/CO atmosphere and lowering temperature indicated conclusively that the reduction of both complexes couples to a chemical reaction which involves CO-loss. 相似文献
952.
Platinum–cobalt (PtCo) alloy nanoparticles (NPs) are successfully fabricated by ultrasonic-electrodeposition method, using an inclusion complex (IC) film of functionalized cyclodextrin (CD)–ionic liquid (IL) as support. The morphology and composition of the PtCo alloy NPs are characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction, respectively. It is found that they are well-dispersed on the CD–IL surface and exhibit many unique features. The resulting modified glassy carbon electrode shows excellent catalytic activity for glucose oxidation. Under the physiological condition, the oxidation current of glucose is linear to its concentration up to 20 mM with sensitivity of 13.7 μA mM?1 cm?2. In addition, the interference from the oxidation of ascorbic acid and uric acid could be effectively avoided. Therefore, it is promising as a nonenzymatic glucose sensor. 相似文献
953.
Yan Li Anhuai Lu Hongrui Ding Xin Wang Changqiu Wang Cuiping Zeng Yunhua Yan 《Electrochemistry communications》2010,12(7):944-947
An investigation aimed at checking the integration of cathodic pyrrhotite Fenton's reaction with anodic microbial respiration for the enhancement of MFC performance and treatment of a real landfill leachate was carried out. The MFC equipped with a pyrrhotite-coated graphite-cathode generated the maximum power density of 4.2 W/m3 that was 133% higher than graphite-cathode. Concomitantly, electrochemical impedance spectroscopy (EIS) showed that the polarization resistance of pyrrhotite-cathode (92 Ω) was much lower than the graphite-cathode (1057 Ω), indicating that the cathodic overpotential was significantly lowered, probably due to the occurrence of pyrrhotite Fenton's reaction. The in situ generation of Fenton's reagents (Fe2+ and H2O2) at the pyrrhotite-cathode was demonstrated by the cyclic voltammetry measurement. Besides, reactive oxygen species produced from the pyrrhotite Fenton's reaction were detected and demonstrated to be vital to the enhancement of MFC power output. Further, the effectiveness of this system was examined by treating an old-aged landfill leachate. 77% of color and 78% of COD were removed from the original leachate, indicating that the pyrrhotite not only acted as a cost-effective cathodic catalyst for MFCs in power generation, but also extended the practical merits of traditional MFCs towards advanced oxidation of biorefractory pollutants. 相似文献
954.
Zhan C Wang X Wei Z Evans DJ Ru X Zeng X Liu X 《Dalton transactions (Cambridge, England : 2003)》2010,39(46):11255-11262
By using "click" chemistry between a diazide and a diiron model complex armed with two alkynyl groups, two polymeric diiron complexes (Poly-Py and Poly-Ph) were prepared. The two polymeric complexes were investigated using infrared spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermal gravimetric analysis (TGA), M?ssbauer spectroscopy, and cyclic voltammetry (Poly-Py only, due to the insolubility of Poly-Ph). To probe the coordinating mode of the diiron units in the two polymeric complexes, two control complexes (3 and 4) were also synthesised using a monoazide. Complexes 3 and 4 were well characterised and the latter was further crystallographically analysed. It turns out that in both complexes (3 and 4) and the two polymeric diiron complexes, one of the two iron atoms in the diiron unit coordinates with one of the triazole N atoms. Our results revealed that both morphologies and properties of Poly-Py and Poly-Ph are significantly affected by the organic moiety of the diazide. Compared to the protonating behaviour of the complexes 3 and 4, Poly-Py exhibited proton resistance. In electrochemical reduction, potentials for the reduction of the diiron units in Poly-Py and hence its catalytic reduction of proton in acetic acid-DMF shifted by over 400 mV compared to those for complexes 3 and 4. It is likely that the polymeric nature of Poly-Py offers the diiron units a "protective" environment in an acidic medium and more positive reduction potential. 相似文献
955.
The geometries and electronic properties of six polymers based on furo[3,4-b]pyridine-type heterocyclics were studied using
density functional theory (DFT) at the B3LYP/6-31G(d) level. Bond lengths, bond critical point (BCP) properties, nucleus-independent
chemical shift (NICS), and Wiberg bond indexes (WBIs) are analyzed and correlated with conduction properties. The changes
of bond length, BCP properties, NICS, and WBIs all show that the conjugational degree is increased with main chain extension.
The changes of NICS also show that the conjugation is stronger in the central section than in the outer section. And the HOMO–LUMO
energy gap (E
g) is decreased steadily upon chain elongation. The results suggest that the six polymers all have lower energy gaps (in the
range of 0.39–0.58 eV), which indicate that these proposed polymers are good candidates for the conductive materials. 相似文献
956.
Li-Min Zeng Hao-Yang Wang Yin-Long Guo 《Journal of the American Society for Mass Spectrometry》2010,21(3):482-485
A fast, selective, and sensitive GC-MS method has been developed and validated for the determination of boric acid in the
drinking water by derivatization with triethanolamine. This analytic strategy successfully converts the inorganic, nonvolatile
boric acid B(OH)3 present in the drinking water to a volatile triethanolamine borate B(OCH2CH2)3N in a quantitive manner, which facilitates the GC measurement. The SIM mode was applied in the analysis and showed high accuracy,
specificity, and reproducibility, as well as reducing the matrix effect effectively. The calibration curve was obtained from
0.01 μg/mL to 10.0 μg/mL with a satisfactory correlation coefficient of 0.9988. The limit of detection for boric acid was 0.04 μg/L. Then the method was applied for detection of the amount of boric acid in bottled drinking water and the results are in
accordance with the reported concentration value of boric acid. This study offers a perspective into the utility of GC-MS
as an alternate quantitative tool for detection of B(OH)3, even for detection of boron in various other samples by digesting the boron compounds to boric acid. 相似文献
957.
A mono‐lancunary keggin‐type decatungstosilicate (SiW11) polyoxometalate (POM) modified by γ‐aminopropyltriethoxysilane (KH550) was incorporated into polyimide (PI) through copolymerization. Nuclear magnetic resonance (NMR), fourier transition infrared spectroscopy (FTIR), and wide angle X‐ray diffraction (WAXD) were used to characterize the structure and composition of the polyoxometalate–organosilane hybrid (SiW11KH550) and PI/SiW11KH550 copolymers. The differential scanning calorimetry (DSC) studies indicate that the glass transition temperature (Tg) of PI/SiW11KH550 copolymers increases from 330°C (for neat PI) to 409°C (for the copolymer sample with 10 wt% of SiW11KH550). Dielectric measurement showed that both the dielectric constant and the dielectric loss for the copolymer thin films decreased with the increase in SiW11KH550 content, and the dielectric constant and dielectric loss values decreased to 2.1 and 3.54 × 10?3, respectively, for the copolymer sample with 10 wt% of SiW11KH550. The incorporation of SiW11KH550 into polymer matrices is a promising approach to prepare PI films with a low dielectric constant and low dielectric loss. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
958.
Two new acylated flavonoid glycosides have been isolated from the leaves of Quercus dentata Thunb. On the basis of chemical and spectral data, the structures of the compounds have been elucidated as kaempferol 3-O-(2", 4"-diacetyl-3"-cis-p-coumaroyl-6"-trans-p-coumaroyl)-beta-D-glucopyranoside (1), and kaempferol 3-O-(2"-trans-p-coumaroyl-3", 4"-diacetyl-6"-cisp-coumaroyl)-beta-D-glucopyranoside (2). 相似文献
959.
960.
乳香大环二萜类化学成分研究 总被引:4,自引:0,他引:4
采用硅胶柱层析,制备薄层层析等色谱方法,从乳香CO_2超临界提取物中分得7个大环二萜类化合物,经波谱方法鉴定为incensole acetate(1),incensole(2),incensole oxide acetate(3),isoincensole acetate(4),incensole oxide(5),isoincensoleoxide(6),isoincensolol(7),其中,化合物7为新化合物,化合物4为首次从该属植物中分离得到.采用四甲基偶氮唑蓝(MTT)法观察化合物对肿瘤细胞的抑制增殖作用. 相似文献