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991.
Tandem mass spectrometry (MS/MS) of intact, noncovalently-bound protein-ligand complexes can yield structural information on the site of ligand binding. Fourier transform ion cyclotron resonance (FT-ICR) top-down MS of the 29 kDa carbonic anhydrase-zinc complex and adenylate kinase bound to adenosine triphosphate (ATP) with collisionally activated dissociation (CAD) and/or electron capture dissociation (ECD) generates product ions that retain the ligand and their identities are consistent with the solution phase structure. Increasing gas phase protein charging from electrospray ionization (ESI) by the addition of supercharging reagents, such as m-nitrobenzyl alcohol and sulfolane, to the protein analyte solution improves the capability of MS/MS to generate holo-product ions. Top-down proteomics for protein sequencing can be enhanced by increasing analyte charging. 相似文献
992.
A sensitive hydrazine sensor has been fabricated using copper oxide nanoparticles modified glassy carbon electrode (GCE) to
form nano-copper oxide/GCE. The nano-copper oxide was electrodeposited on the surface of GCE in CuCl2 solution at −0.4 V and was characterized by Scanning electron microscopy and X-ray diffraction. The prepared modified electrode
showed a good electrocatalytic activity toward oxidation of hydrazine. The electrochemical behavior of hydrazine on nano-copper
oxide/GCE was explored. The oxidative current increased linearly with improving concentration of hydrazine on nano-copper
oxide/GCE from 0.1 to 600 μM and detection limit for hydrazine was evaluated to be 0.03 μM at a signal-to-noise ratio of 3.
The oxidation mechanism of hydrazine on the nano-copper oxide/GCE was also discussed. The fabricated sensor could be used
to determine hydrazine in real water. 相似文献
993.
Quanyi Hao Danni Lei Xiaoming Yin Ming Zhang Shuang Liu Qiuhong Li Libao Chen Taihong Wang 《Journal of Solid State Electrochemistry》2011,15(11-12):2563-2569
Urchin-like nano/micro-structured Fe3O4/C composite has been successfully synthesized using inexpensive starting materials. The urchin-shaped nano/micro-structure consisted of several oriented nanorods. TEM analysis revealed that there is a large number of pores and uniform amorphous carbon distribution at a nanoscale in the nanorods walls. As used in lithium-ion batteries, the mesoporous Fe3O4/C anode delivered a higher reversible capacity of about 830?mAh?g?1 at 0.1?C up to 50 cycles, as well as enhanced high-rate capability compared with urchin-like Fe2O3 and commercial Fe3O4. The improvements can be attributed to the combined effects of the nano/micro-architecture, the porosity, and the ultra-fine carbon matrix, where the three factors would contribute to possess both the merits of nanometer-sized building blocks and micro-sized assemblies and provide high electronic conductivity. It is believed that the results of this study offer new prospects for improving the lithium storage capacity of metal oxides by controlling both architecture and composition. 相似文献
994.
995.
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997.
The electronic and optical properties of InMO(4) (M = V, Nb, Ta) photocatalysts are studied using first-principles calculations. For all InMO(4), the calculated band gaps are larger than the measured optical gaps, indicating the existence of sub-bandgap transitions. Impurity states and excitons are considered to interpret the characteristic absorption onsets in the measured UV-visible diffuse reflection spectra. The novel visible-light-active water-splitting photocatalytic properties of InMO(4) are related to the sub-bandgap transitions. Correlation between the impurity states and the photocatalytic activities is discussed for InMO(4)via the conventional mechanism of photocatalytic water-splitting on semiconductors. An excitonic mechanism analogous to Photosystem II in plant photosynthesis is also proposed for the photocatalytic water-splitting process on InMO(4). 相似文献
998.
In this study, multilayers from polyethylene imine, heparin and chitosan are prepared at three different pH values of 5, 7 and 9. Water contact angle and quartz microbalance measurements show that resulting multilayers differ in terms of wetting behaviour, layer mass and mechanical properties. The multilayer is then formed within a gradient generation microfluidic (μFL) device. Polyethylene imine or heparin solutions of pH 5 are introduced into one inlet and the same solutions but at pH 9 into another inlet of the μFL device. The pH gradient established during the multilayer formation can be visualized inside the microchamber by pH sensitive fluorophores and confocal laser scanning microscopy. From this setup it is expected that properties of multilayers displayed at distinct pH values can be realised in a gradient manner inside the μFL device. Behaviour of the osteoblast cell line MG-63 seeded and cultured on top of multilayers created inside the μFL device support this hypothesis. It is observed that more cells adhere and spread on multilayers build-up at the basic side of the μFL channel, while those cells on top of multilayers built at pH 5 are fewer and smaller. These results are consistent with the behaviour of MG-63 cells seeded on multilayers formed at discrete pH values. It is particularly interesting to see that cells start to migrate from multilayers built at pH 5 to those built at pH 9 during 6 h of culture. Overall, the presented multilayer formation setup applying pH gradients leads to surfaces that promote migration of cells. 相似文献
999.
Dr. Hai‐Feng Xiang Dr. Stephen Sin‐Yin Chui Prof. V. A. L. Roy Prof. Chi‐Ming Che 《化学:亚洲杂志》2011,6(12):3223-3229
Organic photovoltaic (OPV) cells using metal(II) (Pt, Pd, Cu, and Ni) chelates of 8‐hydroxyquinoline (Hq) or 5,7‐dimethyl‐8‐hydroxy‐quinoline (HMe2q) as an electron donor were fabricated by vacuum deposition. The bis(5,7‐dimethyl‐8‐hydroxyquinolinato)platinum(II) [Pt(Me2q)2]‐based OPVs showed the best performance with an open voltage (VOC) of 0.42 V, a short circuit current density (JSC) of 14.8 mA cm?2, and a maximum power conversion efficiency (ηP) of 2.4 %. The X‐ray single‐crystal structures together with the grazing incidence X‐ray diffraction (GIXRD) data of thin film samples reveal that the peripheral methyl substituent(s) and platinum(II) ion are essential for the high degree of film crystallinity resulting in improved performance of the as‐fabricated field‐effect transistors (FETs) and OPV cells. 相似文献
1000.
Dr. Jia Wang Dr. Yong Chen Dr. Yuen‐Chi Law Meiyi Li Dr. Ming‐Xin Zhu Dr. Wei Lu Dr. Stephen Sin‐Yin Chui Dr. Nianyong Zhu Prof. Dr. Chi‐Ming Che 《化学:亚洲杂志》2011,6(11):3011-3019
A series of phosphorescent terpyridyl platinum(II) complexes with ancillary biphenylacetylide ligands, namely, [(R3tpy)PtC≡C(biphenyl)]X (R=tBu, H, or Et2N; tpy=2,2′;6′,2′′‐terpyridyl; X is an anion) were synthesized and structurally characterized by various spectroscopic techniques and X‐ray diffraction methods. Despite a lack of long alkyl chain(s) or hydrogen‐bonding motif(s), complexes [(tpy)PtC≡C(biphenyl)]Cl and [(tBu3tpy)PtC≡C(biphenyl)]X (X=Cl, ClO4, PF6, or BF4) were found to gelate water and organic solvents, respectively. The self‐aggregation of these complexes in solutions and the resulting gels were investigated with variable‐temperature (VT) 1H NMR spectroscopy, polarized optical microscopy, and absorption/emission spectroscopy. SEM micrographs on dry gels revealed entangled nanofibers with diameters of 20–40 nm and lengths of tens of micrometers. Powder X‐ray diffraction (PXRD) study revealed various degrees of crystallinity of these fibrillar nanostructures. The substituents on both the terpyridyl and acetylide ligands and counterion of these complexes play a profound but concerted role in tuning the intermolecular metal???metal and/or π–π interactions, and hence the gelation properties. 相似文献